105 results on '"Guinamard R"'
Search Results
2. The TRPM4 channel inhibitor 9-phenanthrol
- Author
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Guinamard, R, Hof, T, and Del Negro, C A
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- 2014
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3. Characterization of a Ca2+-activated Nonselective Cation Channel during Dedifferentiation of Cultured Rat Ventricular Cardiomyocytes
- Author
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Guinamard, R., Rahmati, M., Lenfant, J., and Bois, P.
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- 2002
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4. 9-Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels
- Author
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Grand, T, Demion, M, Norez, C, Mettey, Y, Launay, P, Becq, F, Bois, P, and Guinamard, R
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- 2008
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5. Effects of internal ph on the nonselective cation channel from the mouse collecting tubule
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Chraïbi, A., Guinamard, R., and Teulon, J.
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- 1995
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6. Lysosomal Cholesterol Hydrolysis Couples Efferocytosis To Anti-Inflammatory Oxysterol Production
- Author
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Ivanov, S., primary, Viaud, M., additional, Vujic, N., additional, Duta-Mare, M., additional, Dugail, I., additional, Hainault, I., additional, Stehlik, C., additional, Marchetti, S., additional, Boyer, L., additional, Guinamard, R., additional, Foufelle, F., additional, Bochem, A., additional, Hovingh, K.G., additional, Thorp, E.B., additional, Gautier, E.L., additional, Kratky, D., additional, and Yvan-Charvet, L., additional
- Published
- 2019
- Full Text
- View/download PDF
7. The SH3 Domain of Bruton's Tyrosine Kinase Interacts with Vav, Sam68 and EWS
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GUINAMARD, R., FOUGEREAU, M., and SECKINGER, P.
- Published
- 1997
8. TRPM4 variants associated with long QT syndrome
- Author
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Thomas, H., primary, Liu, H., additional, Salle, L., additional, Schott, J., additional, Ducreux, C., additional, Millat, G., additional, Chevalier, P., additional, Probst, V., additional, Guinamard, R., additional, and Bouvagnet, P., additional
- Published
- 2017
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9. Argon-induced postconditioning of human myocardium: role of the “reperfusion injury salvage kinases” signalling pathway
- Author
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Lemoine, S., primary, Coulbault, L., additional, Allouche, S., additional, Hanouz, J.-L., additional, Guinamard, R., additional, and Manrique, A., additional
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- 2012
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10. TRPM4, a Ca2+-activated nonselective cation channel in mouse sino-atrial node cells
- Author
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DEMION, M, primary, BOIS, P, additional, LAUNAY, P, additional, and GUINAMARD, R, additional
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- 2007
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11. Calcium-Activated Nonselective Cation Channels in Mammalian Cardiomyocytes
- Author
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GUINAMARD, R, primary, DEMION, M, additional, CHATELIER, A, additional, and BOIS, P, additional
- Published
- 2006
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12. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel.
- Author
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Marvão, P, primary, De Jesus Ferreira, M C, additional, Bailly, C, additional, Paulais, M, additional, Bens, M, additional, Guinamard, R, additional, Moreau, R, additional, Vandewalle, A, additional, and Teulon, J, additional
- Published
- 1998
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13. Inhibition of a small-conductance cAMP-dependent Cl- channel in the mouse thick ascending limb at low internal pH.
- Author
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Guinamard, R, primary, Paulais, M, additional, and Teulon, J, additional
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- 1996
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14. A small-conductance Cl- channel in the mouse thick ascending limb that is activated by ATP and protein kinase A.
- Author
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Guinamard, R, primary, Chraïbi, A, additional, and Teulon, J, additional
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- 1995
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15. Synapse formation and spontaneous activity in rat brainstem neurons in primary culture
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Guinamard, R., Delpy, E., Denizot, J.-P., and Jacquin, T.D.
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- 1999
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16. 380 - TRPM4 variants associated with long QT syndrome.
- Author
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Thomas, H., Liu, H., Salle, L., Schott, J., Ducreux, C., Millat, G., Chevalier, P., Probst, V., Guinamard, R., and Bouvagnet, P.
- Published
- 2017
- Full Text
- View/download PDF
17. EPAC1 and 2 inhibit K + currents via PLC/PKC and NOS/PKG pathways in rat ventricular cardiomyocytes.
- Author
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Boileve A, Romito O, Hof T, Levallois A, Brard L, d'Hers S, Fouchet A, Simard C, Guinamard R, Brette F, and Sallé L
- Subjects
- Animals, Rats, Cyclic GMP-Dependent Protein Kinases metabolism, Nitric Oxide Synthase metabolism, Nitric Oxide Synthase antagonists & inhibitors, Type C Phospholipases metabolism, Type C Phospholipases antagonists & inhibitors, Male, Rats, Wistar, Potassium metabolism, Cyclic AMP metabolism, Guanine Nucleotide Exchange Factors metabolism, Myocytes, Cardiac metabolism, Myocytes, Cardiac drug effects, Myocytes, Cardiac enzymology, Protein Kinase C metabolism, Signal Transduction, Action Potentials drug effects, Heart Ventricles metabolism, Heart Ventricles cytology
- Abstract
The exchange protein directly activated by cAMP (EPAC) has been implicated in cardiac proarrhythmic signaling pathways including spontaneous diastolic Ca
2+ leak from sarcoplasmic reticulum and increased action potential duration (APD) in isolated ventricular cardiomyocytes. The action potential (AP) lengthening following acute EPAC activation is mainly due to a decrease of repolarizing steady-state K+ current (IKSS ) but the mechanisms involved remain unknown. This study aimed to assess the role of EPAC1 and EPAC2 in the decrease of IKSS and to investigate the underlying signaling pathways. AP and K+ currents were recorded with the whole cell configuration of the patch-clamp technique in freshly isolated rat ventricular myocytes. EPAC1 and EPAC2 were pharmacologically activated with 8-(4-chlorophenylthio)-2'- O -methyl-cAMP acetoxymethyl ester (8-CPTAM, 10 µmol/L) and inhibited with R-Ce3F4 and ESI-05, respectively. Inhibition of EPAC1 and EPAC2 significantly decreased the effect of 8-CPTAM on APD and IKSS showing that both EPAC isoforms are involved in these effects. Unexpectedly, calmodulin-dependent protein kinase II (CaMKII) inhibition by AIP or KN-93, and Ca2+ chelation by intracellular BAPTA, did not impact the response to 8-CPTAM. However, inhibition of PLC/PKC and nitric oxide synthase (NOS)/PKG pathways partially prevents the 8-CPTAM-dependent decrease of IKSS . Finally, the cumulative inhibition of PKC and PKG blocked the 8-CPTAM effect, suggesting that these two actors work along parallel pathways to regulate IKSS upon EPAC activation. On the basis of such findings, we propose that EPAC1 and EPAC2 are involved in APD lengthening by inhibiting a K+ current via both PLC/PKC and NOS/PKG pathways. This may have pathological implications since EPAC is upregulated in diseases such as cardiac hypertrophy. NEW & NOTEWORHTY Exchange protein directly activated by cAMP (EPAC) proteins modulate ventricular electrophysiology at the cellular level. Both EPAC1 and EPAC2 isoforms participate in this effect. Mechanistically, PLC/PKC and nitric oxide synthase (NO)/PKG pathways are involved in regulating K+ repolarizing current whereas the well-known downstream effector of EPAC, calmodulin-dependent protein kinase II (CaMKII), does not participate. This may have pathological implications since EPAC is upregulated in diseases such as cardiac hypertrophy. Thus, EPAC inhibition may be a new approach to prevent arrhythmias under pathological conditions.- Published
- 2024
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18. Targeted Radiation Exposure Induces Accelerated Aortic Valve Remodeling in ApoE -/- Mice.
- Author
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Rucher G, Prigent K, Simard C, Frelin AM, Coquemont-Guyot M, Elie N, Delcroix N, Perzo N, Guinamard R, Berger L, Manrique A, and On Behalf Of The Stop-As Investigators
- Abstract
Thoracic radiation therapy may result in accelerated atherosclerosis and in late aortic valve stenosis (AS). In this study, we assessed the feasibility of inducing radiation-induced AS using a targeted aortic valve irradiation (10 or 20 Grays) in two groups of C57Bl6/J (WT) and ApoE
-/- mice compared to a control (no irradiation). Peak aortic jet velocity was evaluated by echocardiography to characterize AS. T2*-weighted magnetic resonance imaging after injection of MPIO-αVCAM-1 was used to examine aortic inflammation resulting from irradiation. A T2* signal void on valve leaflets and aortic sinus was considered positive. Valve remodeling and mineralization were assessed using von Kossa staining. Finally, the impact of radiation on cell viability and cycle from aortic human valvular interstitial cells (hVICs) was also assessed. The targeted aortic valve irradiation in ApoE-/- mice resulted in an AS characterized by an increase in peak aortic jet velocity associated with valve leaflet and aortic sinus remodeling, including mineralization process, at the 3-month follow-up. There was a linear correlation between histological findings and peak aortic jet velocity (r = 0.57, p < 0.01). In addition, irradiation was associated with aortic root inflammation, evidenced by molecular MR imaging ( p < 0.01). No significant effect of radiation exposure was detected on WT animals. Radiation exposure did not affect hVICs viability and cell cycle. We conclude that targeted radiation exposure of the aortic valve in mice results in ApoE-/- , but not in WT, mice in an aortic valve remodeling mimicking the human lesions. This preclinical model could be a useful tool for future assessment of therapeutic interventions., Competing Interests: The authors declare no conflict of interest.- Published
- 2023
- Full Text
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19. TRPM4 contribution in mouse uterine contractions.
- Author
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Fouchet A, Bangando HM, Aize M, Simard C, and Guinamard R
- Subjects
- Female, Pregnancy, Mice, Animals, Calcium metabolism, Oxytocin metabolism, Myometrium metabolism, Uterine Contraction, TRPM Cation Channels metabolism
- Abstract
In Brief: Inappropriate uterine contractions are a matter of concern during pregnancy or menses. We identified the transient receptor potential melastatin 4 (TRPM4) ion channel as a new actor in mouse uterine contractions highlighting this protein as a potential pharmacological target for a better control of myometrial activity., Abstract: Control of uterine contractions is of interest in the context of inappropriate myometrial activity during pregnancy and at time of delivery, but it is also a matter for menstrual pain. While several molecular determinants of myometrial contractions have been described, the complete distribution of roles to the various actors is far from understood. A key phenomenon is a variation in cytoplasmic Ca2+ which leads to the activation of calmodulin in smooth muscle and also in the phosphorylation of myosin allowing contraction. The Ca2+ - TRPM4 channel which is known to modulate Ca2+- fluxes in several cell types was shown to participate in vascular as well as detrusor muscle contraction. We thus designed a study to determine whether it also participates in myometrial contraction. Uterine rings were isolated from Trpm4+/+ and Trpm4-/- non-pregnant adult mice and contractions were recorded using an isometric force transducer. In basal conditions, spontaneous contractions were similar in both groups. Application of 9-phenanthrol, a pharmacological TRPM4 inhibitor, dose-dependently reduced contraction parameters in Trpm4+/+ rings with an IC50 around 2.10-6 mol/L. The effect of 9-phenanthrol was significantly reduced in Trpm4-/- rings. The effect of oxytocin was tested and was found to be stronger in Trpm4+/+ rings compared to Trpm4-/-. Under a constant stimulation by oxytocin, 9-phenanthrol still reduced contraction parameters in Trpm4+/+ rings with a smaller effect on Trpm4-/-. Altogether it indicates that TRPM4 participates in uterine contractions in mice and may thus be evaluated as a new target to control such contractions.
- Published
- 2023
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20. Pathophysiological Roles of the TRPV4 Channel in the Heart.
- Author
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Chaigne S, Barbeau S, Ducret T, Guinamard R, and Benoist D
- Subjects
- Female, Pregnancy, Humans, TRPV Cation Channels metabolism, Endothelial Cells metabolism, Myocytes, Cardiac metabolism, Transient Receptor Potential Channels metabolism, Myocardial Infarction metabolism
- Abstract
The transient receptor potential vanilloid 4 (TRPV4) channel is a non-selective cation channel that is mostly permeable to calcium (Ca
2+ ), which participates in intracellular Ca2+ handling in cardiac cells. It is widely expressed through the body and is activated by a large spectrum of physicochemical stimuli, conferring it a role in a variety of sensorial and physiological functions. Within the cardiovascular system, TRPV4 expression is reported in cardiomyocytes, endothelial cells (ECs) and smooth muscle cells (SMCs), where it modulates mitochondrial activity, Ca2+ homeostasis, cardiomyocytes electrical activity and contractility, cardiac embryonic development and fibroblast proliferation, as well as vascular permeability, dilatation and constriction. On the other hand, TRPV4 channels participate in several cardiac pathological processes such as the development of cardiac fibrosis, hypertrophy, ischemia-reperfusion injuries, heart failure, myocardial infarction and arrhythmia. In this manuscript, we provide an overview of TRPV4 channel implications in cardiac physiology and discuss the potential of the TRPV4 channel as a therapeutic target against cardiovascular diseases.- Published
- 2023
- Full Text
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21. Ion Channels in the Development and Remodeling of the Aortic Valve.
- Author
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Simard C, Aize M, Chaigne S, Mpweme Bangando H, and Guinamard R
- Subjects
- Humans, Aortic Valve pathology, Fibrosis, Aortic Valve Stenosis pathology, Bicuspid Aortic Valve Disease
- Abstract
The role of ion channels is extensively described in the context of the electrical activity of excitable cells and in excitation-contraction coupling. They are, through this phenomenon, a key element for cardiac activity and its dysfunction. They also participate in cardiac morphological remodeling, in particular in situations of hypertrophy. Alongside this, a new field of exploration concerns the role of ion channels in valve development and remodeling. Cardiac valves are important components in the coordinated functioning of the heart by ensuring unidirectional circulation essential to the good efficiency of the cardiac pump. In this review, we will focus on the ion channels involved in both the development and/or the pathological remodeling of the aortic valve. Regarding valve development, mutations in genes encoding for several ion channels have been observed in patients suffering from malformation, including the bicuspid aortic valve. Ion channels were also reported to be involved in the morphological remodeling of the valve, characterized by the development of fibrosis and calcification of the leaflets leading to aortic stenosis. The final stage of aortic stenosis requires, until now, the replacement of the valve. Thus, understanding the role of ion channels in the progression of aortic stenosis is an essential step in designing new therapeutic approaches in order to avoid valve replacement.
- Published
- 2023
- Full Text
- View/download PDF
22. TRPM4 Participates in Irradiation-Induced Aortic Valve Remodeling in Mice.
- Author
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Mpweme Bangando H, Simard C, Aize M, Lebrun A, Manrique A, Guinamard R, and On Behalf Of The Stop-As Investigators
- Abstract
Thoracic radiotherapy can lead to cardiac remodeling including valvular stenosis due to fibrosis and calcification. The monovalent non-selective cation channel TRPM4 is known to be involved in calcium handling and to participate in fibroblast transition to myofibroblasts, a phenomenon observed during aortic valve stenosis. The goal of this study was to evaluate if TRPM4 is involved in irradiation-induced aortic valve damage. Four-month-old Trpm4
+/+ and Trpm4-/- mice received 10 Gy irradiation at the aortic valve. Cardiac parameters were evaluated by echography until 5 months post-irradiation, then hearts were collected for morphological and histological assessments. At the onset of the protocol, Trpm4+/+ and Trpm4-/- mice exhibited similar maximal aortic valve jet velocity and mean pressure gradient. Five months after irradiation, Trpm4+/+ mice exhibited a significant increase in those parameters, compared to the untreated animals while no variation was detected in Trpm4-/- mice. Morphological analysis revealed that irradiated Trpm4+/+ mice exhibited a 53% significant increase in the aortic valve cusp surface while no significant variation was observed in Trpm4-/- animals. Collagen staining revealed aortic valve fibrosis in irradiated Trpm4+/+ mice but not in irradiated Trpm4-/- animals. It indicates that TRPM4 influences irradiation-induced valvular remodeling.- Published
- 2022
- Full Text
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23. Influenza Virus Infection Impairs the Gut's Barrier Properties and Favors Secondary Enteric Bacterial Infection through Reduced Production of Short-Chain Fatty Acids.
- Author
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Sencio V, Gallerand A, Gomes Machado M, Deruyter L, Heumel S, Soulard D, Barthelemy J, Cuinat C, Vieira AT, Barthelemy A, Tavares LP, Guinamard R, Ivanov S, Grangette C, Teixeira MM, Foligné B, Wolowczuk I, Le Goffic R, Thomas M, and Trottein F
- Subjects
- Disease Susceptibility, Dysbiosis, Enterobacteriaceae Infections metabolism, Humans, Influenza, Human metabolism, Intestinal Mucosa immunology, Enterobacteriaceae Infections etiology, Fatty Acids, Volatile biosynthesis, Host-Pathogen Interactions immunology, Influenza A virus physiology, Influenza, Human complications, Influenza, Human virology, Intestinal Mucosa metabolism, Microbial Interactions
- Abstract
Along with respiratory tract disease per se , viral respiratory infections can also cause extrapulmonary complications with a potentially critical impact on health. In the present study, we used an experimental model of influenza A virus (IAV) infection to investigate the nature and outcome of the associated gut disorders. In IAV-infected mice, the signs of intestinal injury and inflammation, altered gene expression, and compromised intestinal barrier functions peaked on day 7 postinfection. As a likely result of bacterial component translocation, gene expression of inflammatory markers was upregulated in the liver. These changes occurred concomitantly with an alteration of the composition of the gut microbiota and with a decreased production of the fermentative, gut microbiota-derived products short-chain fatty acids (SCFAs). Gut inflammation and barrier dysfunction during influenza were not attributed to reduced food consumption, which caused in part gut dysbiosis. Treatment of IAV-infected mice with SCFAs was associated with an enhancement of intestinal barrier properties, as assessed by a reduction in the translocation of dextran and a decrease in inflammatory gene expression in the liver. Lastly, SCFA supplementation during influenza tended to reduce the translocation of the enteric pathogen Salmonella enterica serovar Typhimurium and to enhance the survival of doubly infected animals. Collectively, influenza virus infection can remotely impair the gut's barrier properties and trigger secondary enteric infections. The latter phenomenon can be partially countered by SCFA supplementation.
- Published
- 2021
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24. TRPA1 and TRPV1, do we hold you in our heart?
- Author
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Guinamard R and Hof T
- Subjects
- Humans, TRPA1 Cation Channel, TRPV Cation Channels, Transient Receptor Potential Channels
- Published
- 2021
- Full Text
- View/download PDF
25. TRPM4 Participates in Aldosterone-Salt-Induced Electrical Atrial Remodeling in Mice.
- Author
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Simard C, Ferchaud V, Sallé L, Milliez P, Manrique A, Alexandre J, and Guinamard R
- Subjects
- Action Potentials, Aldosterone, Animals, Arrhythmias, Cardiac chemically induced, Arrhythmias, Cardiac genetics, Arrhythmias, Cardiac physiopathology, Connexin 43 metabolism, Disease Models, Animal, Heart Atria physiopathology, Male, Mice, Inbred C57BL, Mice, Knockout, Sodium Chloride, Dietary, TRPM Cation Channels genetics, Time Factors, Mice, Arrhythmias, Cardiac metabolism, Atrial Function, Left, Atrial Remodeling, Heart Atria metabolism, Heart Rate, TRPM Cation Channels metabolism
- Abstract
Aldosterone plays a major role in atrial structural and electrical remodeling, in particular through Ca
2+ -transient perturbations and shortening of the action potential. The Ca2+ -activated non-selective cation channel Transient Receptor Potential Melastatin 4 (TRPM4) participates in atrial action potential. The aim of our study was to elucidate the interactions between aldosterone and TRPM4 in atrial remodeling and arrhythmias susceptibility. Hyperaldosteronemia, combined with a high salt diet, was induced in mice by subcutaneously implanted osmotic pumps during 4 weeks, delivering aldosterone or physiological serum for control animals. The experiments were conducted in wild type animals ( Trpm4+/+ ) as well as Trpm4 knock-out animals ( Trpm4-/- ). The atrial diameter measured by echocardiography was higher in Trpm4-/- compared to Trpm4+/+ animals, and hyperaldosteronemia-salt produced a dilatation in both groups. Action potentials duration and triggered arrhythmias were measured using intracellular microelectrodes on the isolated left atrium. Hyperaldosteronemia-salt prolong action potential in Trpm4-/- mice but had no effect on Trpm4+/+ mice. In the control group (no aldosterone-salt treatment), no triggered arrythmias were recorded in Trpm4+/+ mice, but a high level was detected in Trpm4-/- mice. Hyperaldosteronemia-salt enhanced the occurrence of arrhythmias (early as well as delayed-afterdepolarization) in Trpm4+/+ mice but decreased it in Trpm4-/- animals. Atrial connexin43 immunolabelling indicated their disorganization at the intercalated disks and a redistribution at the lateral side induced by hyperaldosteronemia-salt but also by Trpm4 disruption. In addition, hyperaldosteronemia-salt produced pronounced atrial endothelial thickening in both groups. Altogether, our results indicated that hyperaldosteronemia-salt and TRPM4 participate in atrial electrical and structural remodeling. It appears that TRPM4 is involved in aldosterone-induced atrial action potential shortening. In addition, TRPM4 may promote aldosterone-induced atrial arrhythmias, however, the underlying mechanisms remain to be explored.- Published
- 2021
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26. Transient receptor potential vanilloid 4 channel participates in mouse ventricular electrical activity.
- Author
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Chaigne S, Cardouat G, Louradour J, Vaillant F, Charron S, Sacher F, Ducret T, Guinamard R, Vigmond E, and Hof T
- Subjects
- Animals, Calcium Channels, L-Type metabolism, Computer Simulation, HEK293 Cells, Humans, Leucine analogs & derivatives, Leucine pharmacology, Male, Mice, Inbred C57BL, Mice, Knockout, Models, Cardiovascular, Myocytes, Cardiac drug effects, Piperidines pharmacology, Quinolines pharmacology, Sulfonamides pharmacology, TRPV Cation Channels deficiency, TRPV Cation Channels genetics, Time Factors, Mice, Action Potentials drug effects, Calcium Signaling drug effects, Heart Rate drug effects, Myocytes, Cardiac metabolism, TRPV Cation Channels metabolism, Ventricular Function, Left drug effects
- Abstract
The TRPV4 channel is a calcium-permeable channel ( P
Ca / PNa ∼ 10). Its expression has been reported in ventricular myocytes, where it is involved in several cardiac pathological mechanisms. In this study, we investigated the implication of TRPV4 in ventricular electrical activity. Left ventricular myocytes were isolated from trpv4+/+ and trpv4-/- mice. TRPV4 membrane expression and its colocalization with L-type calcium channels (Cav 1.2) was confirmed using Western blot biotinylation, immunoprecipitation, and immunostaining experiments. Then, electrocardiograms (ECGs) and patch-clamp recordings showed shortened QTc and action potential (AP) duration in trpv4-/- compared with trpv4+/+ mice. Thus, TRPV4 activator GSK1016790A produced a transient and dose-dependent increase in AP duration at 90% of repolarization (APD90 ) in trpv4+/+ but not in trpv4-/- myocytes or when combined with TRPV4 inhibitor GSK2193874 (100 nM). Hence, GSK1016790A increased calcium transient (CaT) amplitude in trpv4+/+ but not in trpv4-/- myocytes, suggesting that TRPV4 carries an inward Ca2+ current in myocytes. Conversely, TRPV4 inhibitor GSK2193874 (100 nM) alone reduced APD90 in trpv4+/+ but not in trpv4-/- myocytes, suggesting that TRPV4 prolongs AP duration in basal condition. Finally, introducing TRPV4 parameters in a mathematical model predicted the development of an inward TRPV4 current during repolarization that increases AP duration and CaT amplitude, in accord with what was found experimentally. This study shows for the first time that TRPV4 modulates AP and QTc durations. It would be interesting to evaluate whether TRPV4 could be involved in long QT-mediated ventricular arrhythmias. NEW & NOTEWORTHY Transient receptor potential vanilloid 4 (TRPV4) is expressed at the membrane of mouse ventricular myocytes and colocalizes with non-T-tubular L-type calcium channels. Deletion of trpv4 gene in mice results in shortened QT interval on electrocardiogram and reduced action potential duration of ventricular myocytes. Pharmacological activation of TRPV4 channel leads to increased action potential duration and increased calcium transient amplitude in trpv4-/- but not in trpv4-/- ventricular myocytes. To the contrary, TRPV4 channel pharmacological inhibition reduces action potential duration in trpv4+/+ but not in trpv4-/- myocytes. Integration of TRPV4 channel in a computational model of mouse action potential shows that the channel carries an inward current contributing to slowing down action potential repolarization and to increase calcium transient amplitude, similarly to what is observed experimentally. This study highlights for the first time the involvement of TRPV4 channel in ventricular electrical activity.- Published
- 2021
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27. TRPM4 non-selective cation channel in human atrial fibroblast growth.
- Author
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Simard C, Magaud C, Adjlane R, Dupas Q, Sallé L, Manrique A, Bois P, Faivre JF, and Guinamard R
- Subjects
- Action Potentials, Aged, Animals, Calcium metabolism, Cell Proliferation, Cells, Cultured, Female, Humans, Male, Mice, Myocardium cytology, Myofibroblasts drug effects, Myofibroblasts physiology, Phenanthrenes, Endomyocardial Fibrosis metabolism, Myofibroblasts metabolism, TRPM Cation Channels metabolism
- Abstract
Cardiac fibroblasts play an important role in cardiac matrix turnover and are involved in cardiac fibrosis development. Ca
2+ is a driving belt in this phenomenon. This study evaluates the functional expression and contribution of the Ca2+ -activated channel TRPM4 in atrial fibroblast phenotype. Molecular and electrophysiological investigations were conducted in human atrial fibroblasts in primary culture and in atrial fibroblasts obtained from wild-type and transgenic mice with disrupted Trpm4 gene (Trpm4-/- ). A typical TRPM4 current was recorded on human cells (equal selectivity for Na+ and K+ , activation by internal Ca2+ , voltage sensitivity, conductance of 23.2 pS, inhibition by 9-phenanthrol (IC50 = 6.1 × 10-6 mol L-1 )). Its detection rate was 13% on patches at days 2-4 in culture but raised to 100% on patches at day 28. By the same time, a cell growth was observed. This growth was smaller when cells were maintained in the presence of 9-phenanthrol. Similar cell growth was measured on wild-type mice atrial fibroblasts during culture. However, this growth was minimized on Trpm4-/- mice fibroblasts compared to control animals. In addition, the expression of alpha smooth muscle actin increased during culture of atrial fibroblasts from wild-type mice. This was not observed in Trpm4-/- mice fibroblasts. It is concluded that TRPM4 participates in fibroblast growth and could thus be involved in cardiac fibrosis.- Published
- 2020
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28. ABCA1 Exerts Tumor-Suppressor Function in Myeloproliferative Neoplasms.
- Author
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Viaud M, Abdel-Wahab O, Gall J, Ivanov S, Guinamard R, Sore S, Merlin J, Ayrault M, Guilbaud E, Jacquel A, Auberger P, Wang N, Levine RL, Tall AR, and Yvan-Charvet L
- Subjects
- ATP Binding Cassette Transporter 1 deficiency, ATP Binding Cassette Transporter 1 genetics, Animals, Cell Line, Tumor, Cell Transformation, Neoplastic pathology, Cholesterol metabolism, DNA-Binding Proteins metabolism, Dioxygenases, Hematopoietic Stem Cells metabolism, Humans, Interleukin-3 metabolism, Leukemia, Myelogenous, Chronic, BCR-ABL Positive metabolism, Leukemia, Myelogenous, Chronic, BCR-ABL Positive pathology, Lipoproteins, HDL metabolism, Loss of Function Mutation genetics, Mice, Mice, Inbred C57BL, Myelopoiesis, Myeloproliferative Disorders pathology, Proto-Oncogene Proteins metabolism, Signal Transduction, Splenomegaly pathology, ATP Binding Cassette Transporter 1 metabolism, Myeloproliferative Disorders metabolism
- Abstract
Defective cholesterol efflux pathways in mice promote the expansion of hematopoietic stem and progenitor cells and a bias toward the myeloid lineage, as observed in chronic myelomonocytic leukemia (CMML). Here, we identify 5 somatic missense mutations in ABCA1 in 26 patients with CMML. These mutations confer a proliferative advantage to monocytic leukemia cell lines in vitro. In vivo inactivation of ABCA1 or expression of ABCA1 mutants in hematopoietic cells in the setting of Tet2 loss demonstrates a myelosuppressive function of ABCA1. Mechanistically, ABCA1 mutations impair the tumor-suppressor functions of WT ABCA1 in myeloproliferative neoplasms by increasing the IL-3Rβ signaling via MAPK and JAK2 and subsequent metabolic reprogramming. Overexpression of a human apolipoprotein A-1 transgene dampens myeloproliferation. These findings identify somatic mutations in ABCA1 that subvert its anti-proliferative and cholesterol efflux functions and permit the progression of myeloid neoplasms. Therapeutic increases in HDL bypass these defects and restore normal hematopoiesis., Competing Interests: Declaration of Interests R.L.L. is on the supervisory board of QIAGEN and is a scientific advisor to Loxo, Imago, C4 Therapeutics, and Isoplexis, each of which include an equity interest. He receives research support from and has consulted for Celgene and Roche, has received research support from Prelude Therapeutics, and has consulted for Astellas, Incyte, Janssen, Morphosys, and Novartis. He has received honoraria from Lilly and Amgen for invited lectures and from Gilead for grant reviews. The authors have filed a patent, EB19024, on the use of HDL-raising therapies in the treatment of myeloproliferative neoplasms., (Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Published
- 2020
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29. Transient receptor potential channels in cardiac health and disease.
- Author
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Hof T, Chaigne S, Récalde A, Sallé L, Brette F, and Guinamard R
- Subjects
- Action Potentials, Animals, Cardiovascular Agents therapeutic use, Fibroblasts drug effects, Heart Diseases drug therapy, Heart Diseases physiopathology, Humans, Molecular Targeted Therapy, Myocytes, Cardiac drug effects, Purkinje Fibers drug effects, Purkinje Fibers physiopathology, Signal Transduction, Sinoatrial Node drug effects, Sinoatrial Node physiopathology, Transient Receptor Potential Channels drug effects, Fibroblasts metabolism, Heart Diseases metabolism, Myocytes, Cardiac metabolism, Purkinje Fibers metabolism, Sinoatrial Node metabolism, Transient Receptor Potential Channels metabolism
- Abstract
Transient receptor potential (TRP) channels are nonselective cationic channels that are generally Ca
2+ permeable and have a heterogeneous expression in the heart. In the myocardium, TRP channels participate in several physiological functions, such as modulation of action potential waveform, pacemaking, conduction, inotropy, lusitropy, Ca2+ and Mg2+ handling, store-operated Ca2+ entry, embryonic development, mitochondrial function and adaptive remodelling. Moreover, TRP channels are also involved in various pathological mechanisms, such as arrhythmias, ischaemia-reperfusion injuries, Ca2+ -handling defects, fibrosis, maladaptive remodelling, inherited cardiopathies and cell death. In this Review, we present the current knowledge of the roles of TRP channels in different cardiac regions (sinus node, atria, ventricles and Purkinje fibres) and cells types (cardiomyocytes and fibroblasts) and discuss their contribution to pathophysiological mechanisms, which will help to identify the best candidates for new therapeutic targets among the cardiac TRP family.- Published
- 2019
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30. Trpm4 ion channels in pre-Bötzinger complex interneurons are essential for breathing motor pattern but not rhythm.
- Author
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Picardo MCD, Sugimura YK, Dorst KE, Kallurkar PS, Akins VT, Ma X, Teruyama R, Guinamard R, Kam K, Saha MS, and Del Negro CA
- Subjects
- Aging physiology, Animals, Behavior, Animal, Female, Male, Mice, RNA, Messenger genetics, RNA, Messenger metabolism, RNA, Small Interfering metabolism, TRPC Cation Channels genetics, TRPC Cation Channels metabolism, TRPM Cation Channels genetics, Wakefulness, Interneurons metabolism, Motor Activity, Respiration, TRPM Cation Channels metabolism
- Abstract
Inspiratory breathing movements depend on pre-Bötzinger complex (preBötC) interneurons that express calcium (Ca2+)-activated nonselective cationic current (ICAN) to generate robust neural bursts. Hypothesized to be rhythmogenic, reducing ICAN is predicted to slow down or stop breathing; its contributions to motor pattern would be reflected in the magnitude of movements (output). We tested the role(s) of ICAN using reverse genetic techniques to diminish its putative ion channels Trpm4 or Trpc3 in preBötC neurons in vivo. Adult mice transduced with Trpm4-targeted short hairpin RNA (shRNA) progressively decreased the tidal volume of breaths yet surprisingly increased breathing frequency, often followed by gasping and fatal respiratory failure. Mice transduced with Trpc3-targeted shRNA survived with no changes in breathing. Patch-clamp and field recordings from the preBötC in mouse slices also showed an increase in the frequency and a decrease in the magnitude of preBötC neural bursts in the presence of Trpm4 antagonist 9-phenanthrol, whereas the Trpc3 antagonist pyrazole-3 (pyr-3) showed inconsistent effects on magnitude and no effect on frequency. These data suggest that Trpm4 mediates ICAN, whose influence on frequency contradicts a direct role in rhythm generation. We conclude that Trpm4-mediated ICAN is indispensable for motor output but not the rhythmogenic core mechanism of the breathing central pattern generator., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2019
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31. Lysosomal Cholesterol Hydrolysis Couples Efferocytosis to Anti-Inflammatory Oxysterol Production.
- Author
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Viaud M, Ivanov S, Vujic N, Duta-Mare M, Aira LE, Barouillet T, Garcia E, Orange F, Dugail I, Hainault I, Stehlik C, Marchetti S, Boyer L, Guinamard R, Foufelle F, Bochem A, Hovingh KG, Thorp EB, Gautier EL, Kratky D, Dasilva-Jardine P, and Yvan-Charvet L
- Subjects
- Animals, Apoptosis, Biological Transport, Cholesterol Esters metabolism, Erythrocytes metabolism, Hydrolysis, Hypercholesterolemia metabolism, Inflammasomes metabolism, Liver X Receptors metabolism, Lymphocytes metabolism, Mice, Mice, Inbred C57BL, Mitochondria metabolism, NLR Family, Pyrin Domain-Containing 3 Protein metabolism, Neuropeptides metabolism, Receptors, LDL metabolism, Splenomegaly metabolism, Sterol Esterase antagonists & inhibitors, rac1 GTP-Binding Protein metabolism, Cholesterol metabolism, Inflammation metabolism, Lysosomes metabolism, Macrophages metabolism, Oxysterols metabolism, Sterol Esterase metabolism
- Abstract
Rationale: Macrophages face a substantial amount of cholesterol after the ingestion of apoptotic cells, and the LIPA (lysosomal acid lipase) has a major role in hydrolyzing cholesteryl esters in the endocytic compartment., Objective: Here, we directly investigated the role of LIPA-mediated clearance of apoptotic cells both in vitro and in vivo., Methods and Results: We show that LIPA inhibition causes a defective efferocytic response because of impaired generation of 25-hydroxycholesterol and 27-hydroxycholesterol. Reduced synthesis of 25-hydroxycholesterol after LIPA inhibition contributed to defective mitochondria-associated membrane leading to mitochondrial oxidative stress-induced NLRP3 (NOD-like receptor family, pyrin domain containing) inflammasome activation and caspase-1-dependent Rac1 (Ras-related C3 botulinum toxin substrate 1) degradation. A secondary event consisting of failure to appropriately activate liver X receptor-mediated pathways led to mitigation of cholesterol efflux and apoptotic cell clearance. In mice, LIPA inhibition caused defective clearance of apoptotic lymphocytes and stressed erythrocytes by hepatic and splenic macrophages, culminating in splenomegaly and splenic iron accumulation under hypercholesterolemia., Conclusions: Our findings position lysosomal cholesterol hydrolysis as a critical process that prevents metabolic inflammation by enabling efficient macrophage apoptotic cell clearance., (© 2018 American Heart Association, Inc.)
- Published
- 2018
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32. Argon Exposure Induces Postconditioning in Myocardial Ischemia-Reperfusion.
- Author
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Lemoine S, Blanchart K, Souplis M, Lemaitre A, Legallois D, Coulbault L, Simard C, Allouche S, Abraini JH, Hanouz JL, Rouet R, Sallé L, Guinamard R, and Manrique A
- Subjects
- Animals, Atrial Appendage drug effects, Atrial Appendage physiopathology, Guinea Pigs, Humans, Male, Myocardial Reperfusion Injury physiopathology, Organ Culture Techniques, Rats, Rats, Wistar, Argon administration & dosage, Ischemic Postconditioning methods, Myocardial Reperfusion methods, Myocardial Reperfusion Injury prevention & control
- Abstract
Background and Purpose: Cardioprotection against ischemia-reperfusion (I/R) damages remains a major concern during prehospital management of acute myocardial infarction. Noble gases have shown beneficial effects in preconditioning studies. Because emergency proceedings in the context of myocardial infarction require postconditioning strategies, we evaluated the effects of argon in such protocols on mammalian cardiac tissue., Experimental Approaches: In rat, cardiac I/R was induced in vivo by transient coronary artery ligature and cardiac functions were evaluated by magnetic resonance imaging. Hypoxia-reoxygenation (H/R)-induced arrhythmias were evaluated in vitro using intracellular microelectrodes on both rat-isolated ventricle and a model of border zone in guinea pig ventricle. Hypoxia-reoxygenation loss of contractile force was assessed in human atrial appendages. In those models, postconditioning was induced by 5 minutes application of argon at the time of reperfusion., Key Results: In the in vivo model, I/R produced left ventricular ejection fraction decrease (24%) and wall motion score increase (36%) which was prevented when argon was applied in postconditioning. In vitro, argon postconditioning abolished H/R-induced arrhythmias such as early after depolarizations, conduction blocks, and reentries. Recovery of contractile force in human atrial appendages after H/R was enhanced in the argon group, increasing from 51% ± 2% in the nonconditioned group to 83% ± 7% in the argon-treated group ( P < .001). This effect of argon was abolished in the presence of wortmannin and PD98059 which inhibit prosurvival phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt) and MEK/extracellular receptor kinase 1/2 (ERK 1/2), respectively, or in the presence of the mitochondrial permeability transition pore opener atractyloside, suggesting the involvement of the reperfusion injury salvage kinase pathway., Conclusion and Implications: Argon has strong cardioprotective properties when applied in conditions of postconditioning and thus appears as a potential therapeutic tool in I/R situations.
- Published
- 2017
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33. TRPM4 non-selective cation channel variants in long QT syndrome.
- Author
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Hof T, Liu H, Sallé L, Schott JJ, Ducreux C, Millat G, Chevalier P, Probst V, Guinamard R, and Bouvagnet P
- Subjects
- Adolescent, Adult, Aged, Child, Child, Preschool, Female, Humans, Infant, Male, Middle Aged, Young Adult, Amino Acid Substitution, Long QT Syndrome genetics, Long QT Syndrome physiopathology, TRPM Cation Channels genetics
- Abstract
Background: Long QT syndrome (LQTS) is an inherited arrhythmic disorder characterized by prolongation of the QT interval, a risk of syncope, and sudden death. There are already a number of causal genes in LQTS, but not all LQTS patients have an identified mutation, which suggests LQTS unknown genes., Methods: A cohort of 178 LQTS patients, with no mutations in the 3 major LQTS genes (KCNQ1, KCNH2, and SCN5A), was screened for mutations in the transient potential melastatin 4 gene (TRPM4)., Results: Four TRPM4 variants (2.2% of the cohort) were found to change highly conserved amino-acids and were either very rare or absent from control populations. Therefore, these four TRPM4 variants were predicted to be disease causing. Furthermore, no mutations were found in the DNA of these TRPM4 variant carriers in any of the 13 major long QT syndrome genes. Two of these variants were further studied by electrophysiology (p.Val441Met and p.Arg499Pro). Both variants showed a classical TRPM4 outward rectifying current, but the current was reduced by 61 and 90% respectively, compared to wild type TRPM4 current., Conclusions: This study supports the view that TRPM4 could account for a small percentage of LQTS patients. TRPM4 contribution to the QT interval might be multifactorial by modulating whole cell current but also, as shown in Trpm4
-/- mice, by modulating cardiomyocyte proliferation. TRPM4 enlarges the subgroup of LQT genes (KCNJ2 in Andersen syndrome and CACNA1C in Timothy syndrome) known to increase the QT interval through a more complex pleiotropic effect than merely action potential alteration.- Published
- 2017
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34. Disruption of Glut1 in Hematopoietic Stem Cells Prevents Myelopoiesis and Enhanced Glucose Flux in Atheromatous Plaques of ApoE(-/-) Mice.
- Author
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Sarrazy V, Viaud M, Westerterp M, Ivanov S, Giorgetti-Peraldi S, Guinamard R, Gautier EL, Thorp EB, De Vivo DC, and Yvan-Charvet L
- Subjects
- Animals, Aorta, Thoracic metabolism, Apolipoproteins E deficiency, Bone Marrow Transplantation, Cell Division, Cytokine Receptor Common beta Subunit physiology, Disease Progression, Energy Metabolism, Gene Expression Regulation, Glucose Transporter Type 1 deficiency, Glycolysis, Hypercholesterolemia genetics, Hypoxia-Inducible Factor 1, alpha Subunit deficiency, Hypoxia-Inducible Factor 1, alpha Subunit physiology, Metformin pharmacology, Mice, Mice, Inbred C57BL, Mice, Knockout, Multipotent Stem Cells metabolism, RNA, Messenger biosynthesis, RNA, Messenger genetics, Receptors, Interleukin-3 antagonists & inhibitors, Receptors, Interleukin-3 physiology, Spleen metabolism, Tyrphostins pharmacology, Glucose metabolism, Glucose Transporter Type 1 physiology, Hematopoietic Stem Cells metabolism, Hypercholesterolemia metabolism, Myelopoiesis physiology, Plaque, Atherosclerotic metabolism
- Abstract
Rationale: Inflamed atherosclerotic plaques can be visualized by noninvasive positron emission and computed tomographic imaging with (18)F-fluorodeoxyglucose, a glucose analog, but the underlying mechanisms are poorly understood., Objective: Here, we directly investigated the role of Glut1-mediated glucose uptake in apolipoprotein E-deficient (ApoE(-/-)) mouse model of atherosclerosis., Methods and Results: We first showed that the enhanced glycolytic flux in atheromatous plaques of ApoE(-/-) mice was associated with the enhanced metabolic activity of hematopoietic stem and multipotential progenitor cells and higher Glut1 expression in these cells. Mechanistically, the regulation of Glut1 in ApoE(-/-) hematopoietic stem and multipotential progenitor cells was not because of alterations in hypoxia-inducible factor 1α signaling or the oxygenation status of the bone marrow but was the consequence of the activation of the common β subunit of the granulocyte-macrophage colony-stimulating factor/interleukin-3 receptor driving glycolytic substrate utilization by mitochondria. By transplanting bone marrow from WT, Glut1(+/-), ApoE(-/-), and ApoE(-/-)Glut1(+/-) mice into hypercholesterolemic ApoE-deficient mice, we found that Glut1 deficiency reversed ApoE(-/-) hematopoietic stem and multipotential progenitor cell proliferation and expansion, which prevented the myelopoiesis and accelerated atherosclerosis of ApoE(-/-) mice transplanted with ApoE(-/-) bone marrow and resulted in reduced glucose uptake in the spleen and aortic arch of these mice., Conclusions: We identified that Glut1 connects the enhanced glucose uptake in atheromatous plaques of ApoE(-/-) mice with their myelopoiesis through regulation of hematopoietic stem and multipotential progenitor cell maintenance and myelomonocytic fate and suggests Glut1 as potential drug target for atherosclerosis., (© 2016 American Heart Association, Inc.)
- Published
- 2016
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35. TRPM4 non-selective cation channels influence action potentials in rabbit Purkinje fibres.
- Author
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Hof T, Sallé L, Coulbault L, Richer R, Alexandre J, Rouet R, Manrique A, and Guinamard R
- Subjects
- Animals, Calcium metabolism, Cells, Cultured, Female, Myocytes, Cardiac physiology, Potassium metabolism, Purkinje Fibers cytology, Purkinje Fibers physiology, Rabbits, Sodium metabolism, Action Potentials, Myocytes, Cardiac metabolism, Purkinje Fibers metabolism, TRPM Cation Channels metabolism
- Abstract
Key Points: The transient receptor potential melastatin 4 (TRPM4) inhibitor 9-phenanthrol reduces action potential duration in rabbit Purkinje fibres but not in ventricle. TRPM4-like single channel activity is observed in isolated rabbit Purkinje cells but not in ventricular cells. The TRPM4-like current develops during the notch and early repolarization phases of the action potential in Purkinje cells., Abstract: Transient receptor potential melastatin 4 (TRPM4) Ca(2+)-activated non-selective cation channel activity has been recorded in cardiomyocytes and sinus node cells from mammals. In addition, TRPM4 gene mutations are associated with human diseases of cardiac conduction, suggesting that TRPM4 plays a role in this aspect of cardiac function. Here we evaluate the TRPM4 contribution to cardiac electrophysiology of Purkinje fibres. Ventricular strips with Purkinje fibres were isolated from rabbit hearts. Intracellular microelectrodes recorded Purkinje fibre activity and the TRPM4 inhibitor 9-phenanthrol was applied to unmask potential TRPM4 contributions to the action potential. 9-Phenanthrol reduced action potential duration measured at the point of 50 and 90% repolarization with an EC50 of 32.8 and 36.1×10(-6) mol l(-1), respectively, but did not modulate ventricular action potentials. Inside-out patch-clamp recordings were used to monitor TRPM4 activity in isolated Purkinje cells. TRPM4-like single channel activity (conductance = 23.8 pS; equal permeability for Na(+) and K(+); sensitivity to voltage, Ca(2+) and 9-phenanthrol) was observed in 43% of patches from Purkinje cells but not from ventricular cells (0/16). Action potential clamp experiments performed in the whole-cell configuration revealed a transient inward 9-phenanthrol-sensitive current (peak density = -0.65 ± 0.15 pA pF(-1); n = 5) during the plateau phases of the Purkinje fibre action potential. These results show that TRPM4 influences action potential characteristics in rabbit Purkinje fibres and thus could modulate cardiac conduction and be involved in triggering arrhythmias., (© 2015 The Authors. The Journal of Physiology © 2015 The Physiological Society.)
- Published
- 2016
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36. Maintenance of Macrophage Redox Status by ChREBP Limits Inflammation and Apoptosis and Protects against Advanced Atherosclerotic Lesion Formation.
- Author
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Sarrazy V, Sore S, Viaud M, Rignol G, Westerterp M, Ceppo F, Tanti JF, Guinamard R, Gautier EL, and Yvan-Charvet L
- Subjects
- Animals, Apoptosis drug effects, Atherosclerosis genetics, Atherosclerosis metabolism, Atherosclerosis pathology, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Bone Marrow Cells drug effects, Bone Marrow Cells immunology, Bone Marrow Cells pathology, Female, Gene Expression Regulation, Glucose metabolism, Glycolysis genetics, Humans, Inflammation, Lipoproteins, LDL pharmacology, Macrophage Activation drug effects, Macrophages drug effects, Macrophages pathology, Mice, Mice, Knockout, Nuclear Proteins genetics, Nuclear Proteins metabolism, Oxidation-Reduction, Plaque, Atherosclerotic genetics, Plaque, Atherosclerotic metabolism, Plaque, Atherosclerotic pathology, Primary Cell Culture, Receptors, LDL deficiency, Receptors, LDL genetics, Signal Transduction, Toll-Like Receptor 4 genetics, Toll-Like Receptor 4 immunology, Toll-Like Receptor 4 metabolism, Transcription Factors genetics, Transcription Factors metabolism, Atherosclerosis immunology, Macrophages immunology, Nuclear Proteins immunology, Plaque, Atherosclerotic immunology, Receptors, LDL immunology, Transcription Factors immunology
- Abstract
Enhanced glucose utilization can be visualized in atherosclerotic lesions and may reflect a high glycolytic rate in lesional macrophages, but its causative role in plaque progression remains unclear. We observe that the activity of the carbohydrate-responsive element binding protein ChREBP is rapidly downregulated upon TLR4 activation in macrophages. ChREBP inactivation refocuses cellular metabolism to a high redox state favoring enhanced inflammatory responses after TLR4 activation and increased cell death after TLR4 activation or oxidized LDL loading. Targeted deletion of ChREBP in bone marrow cells resulted in accelerated atherosclerosis progression in Ldlr(-/-) mice with increased monocytosis, lesional macrophage accumulation, and plaque necrosis. Thus, ChREBP-dependent macrophage metabolic reprogramming hinders plaque progression and establishes a causative role for leukocyte glucose metabolism in atherosclerosis., (Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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37. TRPM4 in cardiac electrical activity.
- Author
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Guinamard R, Bouvagnet P, Hof T, Liu H, Simard C, and Sallé L
- Subjects
- Action Potentials, Animals, Calcium metabolism, Diastole physiology, Humans, RNA, Messenger analysis, TRPM Cation Channels genetics, Heart physiology, TRPM Cation Channels physiology
- Abstract
TRPM4 forms a non-selective cation channel activated by internal Ca(2+). Its functional expression was demonstrated in cardiomyocytes of several mammalian species including humans, but the channel is also present in many other tissues. The recent characterization of the TRPM4 inhibitor 9-phenanthrol, and the availability of transgenic mice have helped to clarify the role of TRPM4 in cardiac electrical activity, including diastolic depolarization from the sino-atrial node cells in mouse, rat, and rabbit, as well as action potential duration in mouse cardiomyocytes. In rat and mouse, pharmacological inhibition of TRPM4 prevents cardiac ischaemia-reperfusion injuries and decreases the occurrence of arrhythmias. Several studies have identified TRPM4 mutations in patients with inherited cardiac diseases including conduction blocks and Brugada syndrome. This review identifies TRPM4 as a significant actor in cardiac electrophysiology., (Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com.)
- Published
- 2015
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38. Rapid and MR-Independent IK1 Activation by Aldosterone during Ischemia-Reperfusion.
- Author
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Alexandre J, Hof T, Puddu PE, Rouet R, Guinamard R, Manrique A, Beygui F, Sallé L, and Milliez P
- Subjects
- Animals, Female, Heart Ventricles pathology, Male, Myocardial Infarction metabolism, Myocardial Infarction pathology, Myocardial Reperfusion Injury pathology, Myocytes, Cardiac pathology, Rabbits, Aldosterone pharmacology, Heart Ventricles metabolism, Membrane Potentials drug effects, Myocardial Contraction drug effects, Myocardial Reperfusion Injury metabolism, Myocytes, Cardiac metabolism
- Abstract
In ST elevation myocardial infarction (STEMI) context, clinical studies have shown the deleterious effect of high aldosterone levels on ventricular arrhythmia occurrence and cardiac mortality. Previous in vitro reports showed that during ischemia-reperfusion, aldosterone modulates K+ currents involved in the holding of the resting membrane potential (RMP). The aim of this study was to assess the electrophysiological impact of aldosterone on IK1 current during myocardial ischemia-reperfusion. We used an in vitro model of "border zone" using right rabbit ventricle and standard microelectrode technique followed by cell-attached recordings from freshly isolated rabbit ventricular cardiomyocytes. In microelectrode experiments, aldosterone (10 and 100 nmol/L, n=7 respectively) increased the action potential duration (APD) dispersion at 90% between ischemic and normoxic zones (from 95±4 ms to 116±6 ms and 127±5 ms respectively, P<0.05) and reperfusion-induced sustained premature ventricular contractions occurrence (from 2/12 to 5/7 preparations, P<0.05). Conversely, potassium canrenoate 100 nmol/L and RU 28318 1 μmol/l alone did not affect AP parameters and premature ventricular contractions occurrence (except Vmax which was decreased by potassium canrenoate during simulated-ischemia). Furthermore, aldosterone induced a RMP hyperpolarization, evoking an implication of a K+ current involved in the holding of the RMP. Cell-attached recordings showed that aldosterone 10 nmol/L quickly activated (within 6.2±0.4 min) a 30 pS K+-selective current, inward rectifier, with pharmacological and biophysical properties consistent with the IK1 current (NPo =1.9±0.4 in control vs NPo=3.0±0.4, n=10, P<0.05). These deleterious effects persisted in presence of RU 28318, a specific MR antagonist, and were successfully prevented by potassium canrenoate, a non specific MR antagonist, in both microelectrode and patch-clamp recordings, thus indicating a MR-independent IK1 activation. In this ischemia-reperfusion context, aldosterone induced rapid and MR-independent deleterious effects including an arrhythmia substrate (increased APD90 dispersion) and triggered activities (increased premature ventricular contractions occurrence on reperfusion) possibly related to direct IK1 activation.
- Published
- 2015
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39. Proarrhythmic effects of aldosterone during myocardial ischemia-reperfusion: implication of the sarcolemmal-KATP channels.
- Author
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Alexandre J, Puddu PE, Simard C, Hof T, Sallé L, Guinamard R, Manrique A, Rouet R, Beygui F, and Milliez P
- Subjects
- Action Potentials drug effects, Aldosterone pharmacology, Animals, Benzopyrans pharmacology, Dihydropyridines pharmacology, Disease Models, Animal, Female, Glyburide pharmacology, Heart Ventricles drug effects, Heart Ventricles physiopathology, In Vitro Techniques, KATP Channels agonists, KATP Channels antagonists & inhibitors, Male, Myocardial Reperfusion Injury metabolism, Myocardial Reperfusion Injury physiopathology, Perfusion, Rabbits, Aldosterone metabolism, Heart Ventricles metabolism, KATP Channels metabolism, Sarcolemma metabolism
- Abstract
Objective: To assess the electrophysiological impact of aldosterone during myocardial ischemia-reperfusion., Methods: We used an in vitro model of "border zone" using rabbit right ventricle and standard microelectrodes., Results: Aldosterone (10 and 100 nmol/L) shortened ischemic action potential [action potential duration at 90% of repolarization (APD90), from 55 ± 3 to 39 ± 1 ms and 36 ± 3 ms, respectively, P < 0.05] and induced resting membrane potential (RMP) hyperpolarization in the nonischemic zone (from -83 ± 1 to -93 ± 7 mV and -94 ± 3 mV, respectively, P < 0.05) and in the ischemic zone during reperfusion (from -81 ± 2 to -88 ± 2 mV and -91 ± 2 mV, respectively, P < 0.05). Bimakalim, an ATP-sensitive potassium (K(ATP)) channel opener, also induced RMP hyperpolarization and APD90 shortening. Aldosterone (10 and 100 nmol/L) increased APD90 dispersion between ischemic and nonischemic zones (from 96 ± 3 to 117 ± 5 ms and 131 ± 6 ms, respectively, P < 0.05) and reperfusion-induced severe premature ventricular contraction occurrence (from 18% to 67% and 75%, respectively, P < 0.05). Adding glibenclamide, a nonspecific K(ATP) antagonist, to aldosterone superfusion abolished these effects different to sodium 5-hydroxydecanoate, a mitochondrial-K(ATP) antagonist., Conclusions: In this in vitro rabbit model of border zone, aldosterone induced RMP hyperpolarization and decreased ischemic APD90 evoking the modulation of K currents. Glibenclamide prevented these effects different to 5-hydroxydecanoate, suggesting that sarcolemmal-K(ATP) channels may be involved in this context.
- Published
- 2014
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40. Current recordings at the single channel level in adult mammalian isolated cardiomyocytes.
- Author
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Guinamard R, Hof T, and Sallé L
- Subjects
- Animals, Cell Culture Techniques methods, Cell Separation instrumentation, Cells, Cultured, Equipment Design, Heart Atria cytology, Heart Ventricles cytology, Humans, Cell Separation methods, Myocytes, Cardiac cytology, Myocytes, Cardiac metabolism, Patch-Clamp Techniques methods, TRPM Cation Channels metabolism
- Abstract
This chapter describes appropriate methods to investigate mammalian cardiac channels properties at the single channel level. Cell isolation is performed from new born or adult heart by enzymatic digestion on minced tissue or using the Langendorff apparatus. Isolation proceeding is suitable for rabbit, rat, and mouse hearts. In addition, isolation of human atrial cardiomyocytes is described. Such freshly isolated cells or cells maintained in primary culture are suitable for patch-clamp studies. Here we describe the single channel variants of the patch-clamp technique (cell-attached, inside-out, outside-out) used to investigate channel properties. Proceedings for the evaluation of biophysical properties such as conductance, ionic selectivity, regulations by extracellular and intracellular mechanisms are described. To illustrate the study, we provide an example by the characterization of a calcium-activated non-selective cation channel (TRPM4).
- Published
- 2014
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41. Implication of the TRPM4 nonselective cation channel in mammalian sinus rhythm.
- Author
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Hof T, Simard C, Rouet R, Sallé L, and Guinamard R
- Subjects
- Animals, Bradycardia metabolism, Bradycardia physiopathology, Disease Models, Animal, Female, Gene Expression Regulation, Heart Atria pathology, Heart Atria physiopathology, Heart Rate drug effects, Mice, Mice, Inbred C57BL, Patch-Clamp Techniques, Protein Kinase Inhibitors, Rabbits, Rats, Sinoatrial Node metabolism, Sinoatrial Node pathology, TRPM Cation Channels antagonists & inhibitors, TRPM Cation Channels genetics, Bradycardia therapy, Heart Atria metabolism, Heart Rate physiology, Phenanthrenes pharmacology, Sinoatrial Node physiopathology, TRPM Cation Channels biosynthesis
- Abstract
Background: The transient receptor potential melastatin 4 (TRPM4) channel is expressed in the sinoatrial node, but its physiologic roles in this tissue with cardiac pacemaker properties remain unknown. This Ca(2+)-activated nonselective cation channel (NSCCa) induces cell depolarization at negative potentials. It is implicated in burst generation in neurons and participates in induction of ectopic beating in cardiac ventricular preparations submitted to hypoxia/reoxygenation. Accordingly, TRPM4 may participate in action potential (AP) triggering in the sinoatrial node., Objective: The purpose of this study was to investigate the influence of TRPM4 on spontaneous heart beating., Methods: Spontaneous APs were recorded using intracellular microelectrodes in mouse, rat, and rabbit isolated right atria., Results: In the spontaneously beating mouse atrium, superfusion of the TRPM4-specific inhibitor 9-phenanthrol produced a concentration-dependent reduction in AP rate (maximal reduction = 62% that of control; EC50 = 8 × 10(-6) mol●L(-1)) without affecting other AP parameters. These effects were absent in TRPM4(-/-) mice. 9-Phenanthrol exerted a rate-dependent reduction with a higher effect at low rates. Similar results were obtained in rat. Moreover, application of 9-phenanthrol produced a reduction in diastolic depolarization slope in rabbit sinus node pacemaker cells., Conclusion: These data showed that TRPM4 modulates beating rate. Pacemaker activity in the sinoatrial node results from the slow diastolic depolarization slope due to the "funny" current, Na/Ca exchange, and a Ca(2+)-activated nonselective cation current, which can be attributable in part to TRPM4 that may act against bradycardia., (© 2013 Heart Rhythm Society. All rights reserved.)
- Published
- 2013
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42. The TRPM4 non-selective cation channel contributes to the mammalian atrial action potential.
- Author
-
Simard C, Hof T, Keddache Z, Launay P, and Guinamard R
- Subjects
- Action Potentials genetics, Animals, Cells, Cultured, Female, Heart Atria cytology, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Myocytes, Cardiac cytology, Myocytes, Cardiac metabolism, Patch-Clamp Techniques, TRPM Cation Channels genetics, Action Potentials physiology, Heart Atria metabolism, TRPM Cation Channels metabolism
- Abstract
The TRPM4 calcium-activated non-selective monovalent cation channel has been reported in mammalian atrial cardiomyocytes, but its implication in this tissue remains unknown. We used a combination of pharmacological tools and disruption of the Trpm4 gene in mice to investigate the channel implication in atrial action potential (AP). To search for TRPM4 activity, single channel currents were recorded on freshly isolated atrial cardiomyocytes using the patch-clamp technique. To investigate TRPM4 implication in AP, the transmembrane potential was recorded on the multicellular preparation using intracellular microelectrodes after isolating the mouse atrium, under electrical stimulation (rate=5Hz). Isolated atrial cardiomyocytes from the Trpm4(+/+) mouse expressed a typical TRPM4 current while cardiomyocytes from Trpm4(-/-) mouse did not. The Trpm4(+/+) mouse atrium exhibited AP durations at 50, 70 and 90% repolarization of 8.9±0.5ms, 16.0±1.0ms, and 30.2±1.6ms, respectively. The non-selective cation channel inhibitor flufenamic acid (10(-6) and 10(-5)mol·L(-1)) produced a concentration-dependent decrease in AP duration. Similarly, the TRPM4-inhibitor 9-phenanthrol reversibly reduced the duration of AP with an EC50 at 21×10(-6)mol·L(-1), which is similar to that reported for TRPM4 current inhibition in HEK-293 cells. 9-Phenanthrol had no effect on other AP parameters. The effect of 9-phenanthrol is markedly reduced in the mouse ventricle, which displays only weak expression of the channel. Moreover, atria from Trpm4(-/-) mice exhibited an AP that was 20% shorter than that of atria from littermate control mice, and the effect of 9-phenanthrol on AP was abolished in the Trpm4(-/-) mice. Our results showed that TRPM4 is implicated in the waveform of the atrial action potential. It is thus a potential target for pharmacological approaches against atrial arrhythmias., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
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43. Flufenamic acid as an ion channel modulator.
- Author
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Guinamard R, Simard C, and Del Negro C
- Subjects
- Animals, Anti-Inflammatory Agents, Non-Steroidal chemistry, Cell Line, Flufenamic Acid chemistry, Humans, Ion Channels genetics, Patch-Clamp Techniques, Protein Binding, Anti-Inflammatory Agents, Non-Steroidal pharmacology, Flufenamic Acid pharmacology, Ion Channels agonists, Ion Channels antagonists & inhibitors
- Abstract
Flufenamic acid has been known since the 1960s to have anti-inflammatory properties attributable to the reduction of prostaglandin synthesis. Thirty years later, flufenamic acid appeared to be an ion channel modulator. Thus, while its use in medicine diminished, its use in ionic channel research expanded. Flufenamic acid commonly not only affects non-selective cation channels and chloride channels, but also modulates potassium, calcium and sodium channels with effective concentrations ranging from 10(-6)M in TRPM4 channel inhibition to 10(-3)M in two-pore outwardly rectifying potassium channel activation. Because flufenamic acid effects develop and reverse rapidly, it is a convenient and widely used tool. However, given the broad spectrum of its targets, experimental results have to be interpreted cautiously. Here we provide an overview of ion channels targeted by flufenamic acid to aid in interpreting its effects at the molecular, cellular, and system levels. If it is used with good practices, flufenamic acid remains a useful tool for ion channel research. Understanding the targets of FFA may help reevaluate its physiological impacts and revive interest in its therapeutic potential., (Copyright © 2013 Elsevier Inc. All rights reserved.)
- Published
- 2013
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44. Epac activator critically regulates action potential duration by decreasing potassium current in rat adult ventricle.
- Author
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Brette F, Blandin E, Simard C, Guinamard R, and Sallé L
- Subjects
- Adrenergic beta-Agonists pharmacology, Animals, Calcium Signaling, Carbazoles pharmacology, Cells, Cultured, Cyclic AMP pharmacology, Cyclic AMP-Dependent Protein Kinases antagonists & inhibitors, Drug Evaluation, Preclinical, Guanine Nucleotide Exchange Factors agonists, Heart Ventricles cytology, Isoproterenol pharmacology, Male, Myocytes, Cardiac drug effects, Pyrroles pharmacology, Rats, Rats, Wistar, Action Potentials drug effects, Cyclic AMP analogs & derivatives, Guanine Nucleotide Exchange Factors physiology, Myocytes, Cardiac physiology, Potassium metabolism
- Abstract
Sympathetic stimulation is an important modulator of cardiac function via the classic cAMP-dependent signaling pathway, PKA. Recently, this paradigm has been challenged by the discovery of a family of guanine nucleotide exchange proteins directly activated by cAMP (Epac), acting in parallel to the classic signaling pathway. In cardiac myocytes, Epac activation is known to modulate Ca(2+) cycling yet their actions on cardiac ionic currents remain poorly characterized. This study attempts to address this paucity of information using the patch clamp technique to record action potential (AP) and ionic currents on rat ventricular myocytes. Epac was selectively activated by 8-CPT-AM (acetoxymethyl ester form of 8-CPT). AP amplitude, maximum depolarization rate and resting membrane amplitude were unaltered by 8-CPT-AM, strongly suggesting that Na(+) current and inward rectifier K(+) current are not regulated by Epac. In contrast, AP duration was significantly increased by 8-CPT-AM (prolongation of duration at 50% and 90% of repolarization by 41±10% and 43±8% respectively, n=11). L-type Ca(2+) current density was unaltered by 8-CPT-AM (n=16) so this cannot explain the action potential lengthening. However, the steady state component of K(+) current was significantly inhibited by 8-CPT-AM (-38±6%, n=15), while the transient outward K(+) current was unaffected by 8-CPT-AM. These effects were PKA-independent since they were observed in the presence of PKA inhibitor KT5720. Isoprenaline (100nM) induced a significant prolongation of AP duration, even in the presence of KT5720. This study provides the first evidence that the cAMP-binding protein Epac critically modulates cardiac AP duration by decreasing steady state K(+) current. These observations may be relevant to diseases in which Epac is upregulated, like cardiac hypertrophy., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
- Full Text
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45. Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel.
- Author
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Liu H, Chatel S, Simard C, Syam N, Salle L, Probst V, Morel J, Millat G, Lopez M, Abriel H, Schott JJ, Guinamard R, and Bouvagnet P
- Subjects
- Adult, Alleles, Brugada Syndrome mortality, Brugada Syndrome physiopathology, Electrocardiography, Female, Humans, Male, Membrane Potentials genetics, Middle Aged, Sodium Channels genetics, Sodium Channels metabolism, TRPM Cation Channels metabolism, Brugada Syndrome genetics, Death, Sudden, Cardiac, Mutation, TRPM Cation Channels genetics
- Abstract
Brugada syndrome (BrS) is a condition defined by ST-segment alteration in right precordial leads and a risk of sudden death. Because BrS is often associated with right bundle branch block and the TRPM4 gene is involved in conduction blocks, we screened TRPM4 for anomalies in BrS cases. The DNA of 248 BrS cases with no SCN5A mutations were screened for TRPM4 mutations. Among this cohort, 20 patients had 11 TRPM4 mutations. Two mutations were previously associated with cardiac conduction blocks and 9 were new mutations (5 absent from ~14'000 control alleles and 4 statistically more prevalent in this BrS cohort than in control alleles). In addition to Brugada, three patients had a bifascicular block and 2 had a complete right bundle branch block. Functional and biochemical studies of 4 selected mutants revealed that these mutations resulted in either a decreased expression (p.Pro779Arg and p.Lys914X) or an increased expression (p.Thr873Ile and p.Leu1075Pro) of TRPM4 channel. TRPM4 mutations account for about 6% of BrS. Consequences of these mutations are diverse on channel electrophysiological and cellular expression. Because of its effect on the resting membrane potential, reduction or increase of TRPM4 channel function may both reduce the availability of sodium channel and thus lead to BrS.
- Published
- 2013
- Full Text
- View/download PDF
46. A calcium-permeable non-selective cation channel in the thick ascending limb apical membrane of the mouse kidney.
- Author
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Guinamard R, Paulais M, Lourdel S, and Teulon J
- Subjects
- Adenosine Triphosphate metabolism, Animals, Anti-Inflammatory Agents pharmacology, Calcium Signaling drug effects, Flufenamic Acid pharmacology, Hydrogen-Ion Concentration, Ion Channel Gating drug effects, Ion Transport drug effects, Ion Transport physiology, Male, Mice, Calcium metabolism, Calcium Signaling physiology, Ion Channel Gating physiology, Loop of Henle metabolism, TRPM Cation Channels metabolism
- Abstract
Non-selective cation channels have been described in the basolateral membrane of the renal tubule, but little is known about functional channels on the apical side. Apical membranes of microdissected fragments of mouse cortical thick ascending limbs were searched for ion channels using the cell-free configuration of the patch-clamp technique. A cation channel with a linear current-voltage relationship (19pS) that was permeable both to monovalent cations [P(NH4)(1.7)>P(Na) (1.0)=P(K) (1.0)] and to Ca(2+) (P(Ca)/P(Na)≈0.3) was detected. Unlike the basolateral TRPM4 Ca(2+)-impermeable non-selective cation channel, this non-selective cation channel was insensitive to internal Ca(2+), pH and ATP. The channel was already active after patch excision, and its activity increased after reduced pressure was applied via the pipette. External gadolinium (10(-5)M) decreased the channel-open probability by 70% in outside-out patches, whereas external amiloride (10(-4)M) had no effect. Internal flufenamic acid (10(-4)M) inhibited the channel in inside-out patches. Its properties suggest that the current might be supported by the TRPM7 protein that is expressed in the loop of Henle. The conduction properties of the channel suggest that it could be involved in Ca(2+) signaling., (Copyright © 2011 Elsevier B.V. All rights reserved.)
- Published
- 2012
- Full Text
- View/download PDF
47. Transient receptor potential melastatin 4 inhibitor 9-phenanthrol abolishes arrhythmias induced by hypoxia and re-oxygenation in mouse ventricle.
- Author
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Simard C, Sallé L, Rouet R, and Guinamard R
- Subjects
- Action Potentials drug effects, Animals, Arrhythmias, Cardiac etiology, Arrhythmias, Cardiac physiopathology, Calcium Channels drug effects, Female, Flufenamic Acid pharmacology, Heart Ventricles drug effects, Heart Ventricles physiopathology, In Vitro Techniques, Mice, Mice, Inbred C57BL, Myocardial Reperfusion Injury complications, Myocardial Reperfusion Injury physiopathology, Patch-Clamp Techniques, Potassium Channels drug effects, TRPM Cation Channels physiology, Anti-Arrhythmia Agents pharmacology, Arrhythmias, Cardiac drug therapy, Phenanthrenes pharmacology, TRPM Cation Channels antagonists & inhibitors
- Abstract
Background and Purpose: Hypoxia and subsequent re-oxygenation are associated with cardiac arrhythmias such as early afterdepolarizations (EADs), which may be partly explained by perturbations in cytosolic calcium concentration. Transient receptor potential melastatin 4 (TRPM4), a calcium-activated non-selective cation channel, is functionally expressed in the heart. Based on its biophysical properties, it is likely to participate in EADs. Hence, modulators of TRPM4 activity may influence arrhythmias. The aim of this study was to investigate the possible anti-arrhythmic effect of 9-phenanthrol, a TRPM4 inhibitor in a murine heart model of hypoxia and re-oxygenation-induced EADs., Experimental Approach: Mouse heart was removed, and the right ventricle was pinned in a superfusion chamber. After a period of normoxia, the preparation was superfused for 2 h with a hypoxic solution and then re-oxygenated. Spontaneous electrical activity was investigated by intracellular microelectrode recordings., Key Results: In normoxic conditions, the ventricle exhibited spontaneous action potentials. Application of the hypoxia and re-oxygenation protocol unmasked hypoxia-induced EADs, the occurrence of which increased under re-oxygenation. The frequency of these EADs was reduced by superfusion with either flufenamic acid, a blocker of Ca(2+) -dependent cation channels or with 9-phenanthrol. Superfusion with 9-phenanthrol (10(-5) or 10(-4) mol·L(-1) ) caused a dramatic dose-dependent abolition of EADs., Conclusions and Implications: Hypoxia and re-oxygenation-induced EADs can be generated in the mouse heart model. 9-Phenanthrol abolished EADs, which strongly suggests the involvement of TRPM4 in the generation of EAD. This identifies non-selective cation channels inhibitors as new pharmacological candidates in the treatment of arrhythmias., (© 2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society.)
- Published
- 2012
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48. Epithelial-mesenchymal-transition-like and TGFβ pathways associated with autochthonous inflammatory melanoma development in mice.
- Author
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Wehbe M, Soudja SM, Mas A, Chasson L, Guinamard R, de Tenbossche CP, Verdeil G, Van den Eynde B, and Schmitt-Verhulst AM
- Subjects
- Animals, Cell Differentiation, Cell Line, Tumor, Chemokine CCL2 metabolism, Down-Regulation, Enzyme Activation, Humans, JNK Mitogen-Activated Protein Kinases metabolism, MAP Kinase Signaling System, Melanocytes metabolism, Melanocytes pathology, Melanoma, Amelanotic genetics, Melanoma, Amelanotic metabolism, Melanoma, Experimental genetics, Melanoma, Experimental metabolism, Melanoma, Experimental pathology, Mice, Mitogen-Activated Protein Kinases metabolism, Nerve Tissue Proteins genetics, POU Domain Factors genetics, Skin Neoplasms genetics, Skin Neoplasms metabolism, Smad3 Protein metabolism, Up-Regulation, Epithelial-Mesenchymal Transition, Melanoma, Amelanotic pathology, Signal Transduction, Skin Neoplasms pathology, Transforming Growth Factor beta metabolism
- Abstract
We compared gene expression signatures of aggressive amelanotic (Amela) melanomas with those of slowly growing pigmented melanomas (Mela), identifying pathways potentially responsible for the aggressive Amela phenotype. Both tumors develop in mice upon conditional deletion in melanocytes of Ink4a/Arf tumor suppressor genes with concomitant expression of oncogene H-Ras(G12V) and a known tumor antigen. We previously showed that only the aggressive Amela tumors were highly infiltrated by leukocytes concomitant with local and systemic inflammation. We report that Amela tumors present a pattern of de-differentiation with reduced expression of genes involved in pigmentation. This correlates with reduced and enhanced expression, respectively, of microphthalmia-associated (Mitf) and Pou3f2/Brn-2 transcription factors. The reduced expression of Mitf-controlled melanocyte differentiation antigens also observed in some human cutaneous melanoma has important implications for immunotherapy protocols that generally target such antigens. Induced Amela tumors also express Epithelial-Mesenchymal-Transition (EMT)-like and TGFβ-pathway signatures. These are correlated with constitutive Smad3 signaling in Amela tumors and melanoma cell lines. Signatures of infiltrating leukocytes and some chemokines such as chemotactic cytokine ligand 2 (Ccl2) that contribute to leukocyte recruitment further characterize Amela tumors. Inhibition of the mitogen-activated protein kinase (MAPK) activation pathway in Amela tumor lines leads to reduced expression of EMT hallmark genes and inhibits both proinflammatory cytokine Ccl2 gene expression and Ccl2 production by the melanoma cells. These results indicate a link between EMT-like processes and alterations of immune functions, both being controlled by the MAPK pathway. They further suggest that targeting the MAPK pathway within tumor cells will impact tumor-intrinsic oncogenic properties as well as the nature of the tumor microenvironment.
- Published
- 2012
- Full Text
- View/download PDF
49. The non-selective monovalent cationic channels TRPM4 and TRPM5.
- Author
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Guinamard R, Sallé L, and Simard C
- Subjects
- Animals, Biophysics, Calcium Signaling, Humans, Ion Transport, Protein Conformation, TRPM Cation Channels chemistry, TRPM Cation Channels drug effects, TRPM Cation Channels physiology
- Abstract
Transient Receptor Potential (TRP) proteins are non-selective cationic channels with a consistent Ca(2+)-permeability, except for TRPM4 and TRPM5 that are not permeable to this ion. However, Ca(2+) is a major regulator of their activity since both channels are activated by a rise in internal Ca(2+). Thus TRPM4 and TRPM5 are responsible for most of the Ca(2+)-activated non-selective cationic currents (NSC(Ca)) recorded in a large variety of tissues. Their activation induces cell-membrane depolarization that modifies the driving force for ions as well as activity of voltage gated channels and thereby strongly impacts cell physiology. In the last few years, the ubiquitously expressed TRPM4 channel has been implicated in insulin secretion, the immune response, constriction of cerebral arteries, the activity of inspiratory neurons and cardiac dysfunction. Conversely, TRPM5 whose expression is more restricted, has until now been mainly implicated in taste transduction.
- Published
- 2011
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50. Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.
- Author
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Liu H, El Zein L, Kruse M, Guinamard R, Beckmann A, Bozio A, Kurtbay G, Mégarbané A, Ohmert I, Blaysat G, Villain E, Pongs O, and Bouvagnet P
- Subjects
- Animals, CHO Cells, COS Cells, Cardiac Conduction System Disease, Cells, Cultured, Chlorocebus aethiops, Cricetinae, Cricetulus, Family, Female, Genes, Dominant, Genetic Linkage, Heart Block genetics, Heart Block metabolism, Humans, Male, Mutation physiology, Pedigree, TRPM Cation Channels metabolism, TRPM Cation Channels physiology, Transfection, TRPM Cation Channels genetics
- Abstract
Background: Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way., Methods and Results: One Lebanese family and 2 French families with autosomal dominant isolated cardiac conduction blocks were used for linkage analysis. A maximum combined multipoint lod score of 10.5 was obtained on a genomic interval including more than 300 genes. After screening 12 genes of this interval for mutation, we found a heterozygous missense mutation of the TRPM4 gene in each family (p.Arg164Trp, p.Ala432Thr, and p.Gly844Asp). This gene encodes the TRPM4 channel, a calcium-activated nonselective cation channel of the transient receptor potential melastatin (TRPM) ion channel family. All 3 mutations result in an increased current density. This gain of function is due to an elevated TRPM4 channel density at the cell surface secondary to impaired endocytosis and deregulation of Small Ubiquitin MOdifier conjugation (SUMOylation). Furthermore, we showed by immunohistochemistry that TRPM4 channel signal level is higher in atrial cardiomyocytes than in common ventricular cells, but is highest in Purkinje fibers. Small bundles of highly TRPM4-positive cells were found in the subendocardium and in rare intramural bundles., Conclusions: the TRPM4 gene is a causative gene in isolated cardiac conduction disease with mutations resulting in a gain of function and TRPM4 channel being highly expressed in cardiac Purkinje fibers.
- Published
- 2010
- Full Text
- View/download PDF
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