123 results on '"Jonas, Jean-Christophe"'
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2. The lack of functional nicotinamide nucleotide transhydrogenase only moderately contributes to the impairment of glucose tolerance and glucose-stimulated insulin secretion in C57BL/6J vs C57BL/6N mice
- Author
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Close, Anne-Françoise, Chae, Heeyoung, and Jonas, Jean-Christophe
- Published
- 2021
- Full Text
- View/download PDF
3. Metallothionein 1 negatively regulates glucose-stimulated insulin secretion and is differentially expressed in conditions of beta cell compensation and failure in mice and humans
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Bensellam, Mohammed, Shi, Yan-Chuan, Chan, Jeng Yie, Laybutt, D. Ross, Chae, Heeyoung, Abou-Samra, Michel, Pappas, Evan G., Thomas, Helen E., Gilon, Patrick, and Jonas, Jean-Christophe
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- 2019
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4. NNT reverse mode of operation mediates glucose control of mitochondrial NADPH and glutathione redox state in mouse pancreatic β-cells
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Santos, Laila R.B., Muller, Carole, de Souza, Arnaldo H., Takahashi, Hilton K., Spégel, Peter, Sweet, Ian R., Chae, Heeyoung, Mulder, Hindrik, and Jonas, Jean-Christophe
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- 2017
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5. Phlda3 regulates beta cell survival during stress
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Bensellam, Mohammed, Chan, Jeng Yie, Lee, Kailun, Joglekar, Mugdha V., Hardikar, Anandwardhan A., Loudovaris, Thomas, Thomas, Helen E., Jonas, Jean-Christophe, and Laybutt, D. Ross
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- 2019
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6. Prolonged culture of human pancreatic islets under glucotoxic conditions changes their acute beta cell calcium and insulin secretion glucose response curves from sigmoid to bell-shaped
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Tariq, Mohammad, primary, de Souza, Arnaldo H., additional, Bensellam, Mohammed, additional, Chae, Heeyoung, additional, Jaffredo, Manon, additional, Close, Anne-Françoise, additional, Deglasse, Jean-Philippe, additional, Santos, Laila R. B., additional, Buemi, Antoine, additional, Mourad, Nizar I., additional, Wojtusciszyn, Anne, additional, Raoux, Matthieu, additional, Gilon, Patrick, additional, Broca, Christophe, additional, and Jonas, Jean-Christophe, additional
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- 2022
- Full Text
- View/download PDF
7. In depth functional characterization of human induced pluripotent stem cell-derived beta cells in vitro and in vivo
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Fantuzzi, Federica, primary, Toivonen, Sanna, additional, Schiavo, Andrea Alex, additional, Chae, Heeyoung, additional, Tariq, Mohammad, additional, Sawatani, Toshiaki, additional, Pachera, Nathalie, additional, Cai, Ying, additional, Vinci, Chiara, additional, Virgilio, Enrico, additional, Ladriere, Laurence, additional, Suleiman, Mara, additional, Marchetti, Piero, additional, Jonas, Jean-Christophe, additional, Gilon, Patrick, additional, Eizirik, Décio L., additional, Igoillo-Esteve, Mariana, additional, and Cnop, Miriam, additional
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- 2022
- Full Text
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8. Hypoxia reduces ER-to-Golgi protein trafficking and increases cell death by inhibiting the adaptive unfolded protein response in mouse beta cells
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Bensellam, Mohammed, Maxwell, Emma L., Chan, Jeng Yie, Luzuriaga, Jude, West, Phillip K., Jonas, Jean-Christophe, Gunton, Jenny E., and Laybutt, D. Ross
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- 2016
- Full Text
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9. Fertility restoration using immature testicular tissue cryopreserved before gonadotoxic treatment : optimization of the transplantation technique
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UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Wyns, Christine, Poels, Jonathan, des Rieux, Anne, Jonas, Jean-Christophe, Tajeddine, Nicolas, Tombal, Bertrand, Rives, Nathalie, Lybaert, Pascale, Del Vento, Federico, UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Wyns, Christine, Poels, Jonathan, des Rieux, Anne, Jonas, Jean-Christophe, Tajeddine, Nicolas, Tombal, Bertrand, Rives, Nathalie, Lybaert, Pascale, and Del Vento, Federico
- Abstract
Chemotherapy and radiotherapy can induce permanent infertility of the treated patient. For prepubertal boys, no option is currently available for the restauration of fertility after anti-cancer treatments. This represents a major concern that moved several centers all over Europe and North America to develop fertility preservation programs that though experimental, are met with high rates of acceptance by the patients and their parents. As no mature gametes can be found in the testicle before puberty, the only available option is the preservation of spermatogonia, diploid germ cells that are precursors of spermatozoa. Retrieval of immature testicular tissue (ITT) through a small biopsy is a safe and efficient method to preserve germ cells before exposure to gonadotoxic treatments. Amongst the several alternatives currently under-study for fertility restoration, transplantation of frozen-thawed ITT fragments is the most promising option. This procedure has not been performed yet on human subjects, although the xeno-transplantation of such fragments to the nude mice provided a valuable model to study. However, every report on human ITT xeno-transplants described an arrest of spermatogenesis at the pachytene spermatocytes stage and an important germ cells loss. After multiple reports of failed attempts at improving the transplantation procedure through in vivo administration of antioxidants or hormonal supplementation and in vitro culture with supporting molecules before grafting, application of tissue engineering led to promising results in autografts of mice testicular tissue. Indeed, administration of nanoparticles delivering Vascular endothelial growth factor (VEGF) and encapsulation in an alginate matrix improved respectively short-term vascularization and spermatogonial survival. The purpose of our project was to obtain a further improvement of testicular tissue transplantation technique applying tissue engineering. In the first part of the experience, we compare, (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2022
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- 2022
10. Improving ovarian tissue transplantation using adipose tissue-derived stem cells
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UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Dolmans, Marie-Madeleine, Jonas, Jean-Christophe, Jordan, Bénédicte, Andrade Amorim, Christiani, Dehoux, Jean-Paul, Marbaix, Etienne, Herraiz, Sonia, Smitz, Johan, Cacciottola, Luciana, UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Dolmans, Marie-Madeleine, Jonas, Jean-Christophe, Jordan, Bénédicte, Andrade Amorim, Christiani, Dehoux, Jean-Paul, Marbaix, Etienne, Herraiz, Sonia, Smitz, Johan, and Cacciottola, Luciana
- Abstract
Ovarian tissue cryopreservation and further transplantation has proved its effectiveness in restoring fertility after cancer, with over 200 live births worldwide to date. However, it is limited by massive ischemic damage that occurs shortly after transplantation, causing a significant decline in the ovarian reserve. This project aimed to develop a novel strategy using adipose tissue-derived stem cells (ASCs) for ovarian tissue transplantation, after our preliminary results revealed their impact on hypoxia and revascularization. ASCs are able to protect the ovarian reserve from hypoxic damage, thereby reducing follicle loss. Moreover, their secretome, rich in growth factors, is able to both enhance graft revascularization and reperfusion, and mitigate the primordial follicle burn-out due to abnormal activation soon after transplantation. The present work proved the effecicacy of ASC use in ovarian tissue transplantation, which is now one step closer to clinical application., (MED - Sciences médicales) -- UCL, 2022
- Published
- 2022
11. In depth functional characterization of human induced pluripotent stem cell-derived beta cells in vitro and in vivo
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, Fantuzzi, Federica, Toivonen, Sanna, Schiavo, Andrea Alex, Chae, Hee-Young, Tariq, Mohammad, Sawatani, Toshiaki, Pachera, Nathalie, Cai, Ying, Vinci, Chiara, Virgilio, Enrico, Ladriere, Laurence, Suleiman, Mara, Marchetti, Piero, Jonas, Jean-Christophe, Gilon, Patrick, Eizirik, Décio L., Igoillo-Esteve, Mariana, Cnop, Miriam, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, Fantuzzi, Federica, Toivonen, Sanna, Schiavo, Andrea Alex, Chae, Hee-Young, Tariq, Mohammad, Sawatani, Toshiaki, Pachera, Nathalie, Cai, Ying, Vinci, Chiara, Virgilio, Enrico, Ladriere, Laurence, Suleiman, Mara, Marchetti, Piero, Jonas, Jean-Christophe, Gilon, Patrick, Eizirik, Décio L., Igoillo-Esteve, Mariana, and Cnop, Miriam
- Abstract
In vitro differentiation of human induced pluripotent stem cells (iPSCs) into beta cells represents an important cell source for diabetes research. Here, we fully characterized iPSC-derived beta cell function in vitro and in vivo in humanized mice. Using a 7-stage protocol, human iPSCs were differentiated into islet-like aggregates with a yield of insulin-positive beta cells comparable to that of human islets. The last three stages of differentiation were conducted with two different 3D culture systems, rotating suspension or static microwells. In the latter, homogeneously small-sized islet-like aggregates were obtained, while in rotating suspension size was heterogeneous and aggregates often clumped. In vitro function was assessed by glucose-stimulated insulin secretion, NAD(P)H and calcium fluctuations. Stage 7 aggregates slightly increased insulin release in response to glucose in vitro. Aggregates were transplanted under the kidney capsule of NOD-SCID mice to allow for further in vivo beta cell maturation. In transplanted mice, grafts showed glucose-responsiveness and maintained normoglycemia after streptozotocin injection. In situ kidney perfusion assays showed modulation of human insulin secretion in response to different secretagogues. In conclusion, iPSCs differentiated with equal efficiency into beta cells in microwells compared to rotating suspension, but the former had a higher experimental success rate. In vitro differentiation generated aggregates lacking fully mature beta cell function. In vivo, beta cells acquired the functional characteristics typical of human islets. With this technology an unlimited supply of islet-like organoids can be generated from human iPSCs that will be instrumental to study beta cell biology and dysfunction in diabetes.
- Published
- 2022
12. Prolonged culture of human pancreatic islets under glucotoxic conditions changes their acute beta cell calcium and insulin secretion glucose response curves from sigmoid to bell-shaped
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation, Tariq, Mohammad, de Souza, Arnaldo H., Bensellam, Mohammed, Chae, Heeyoung, Jaffredo, Manon, Close, Anne-Françoise, Deglasse, Jean-Philippe, Santos, Laila R. B., Buemi, Antoine, Mourad, Nizar I., Wojtusciszyn, Anne, Raoux, Matthieu, Gilon, Patrick, Broca, Christophe, Jonas, Jean-Christophe, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC/CHEX - Pôle de chirgurgie expérimentale et transplantation, Tariq, Mohammad, de Souza, Arnaldo H., Bensellam, Mohammed, Chae, Heeyoung, Jaffredo, Manon, Close, Anne-Françoise, Deglasse, Jean-Philippe, Santos, Laila R. B., Buemi, Antoine, Mourad, Nizar I., Wojtusciszyn, Anne, Raoux, Matthieu, Gilon, Patrick, Broca, Christophe, and Jonas, Jean-Christophe
- Abstract
Aims/hypothesis: The rapid remission of type 2 diabetes by a diet very low in energy correlates with a marked improvement in glucose-stimulated insulin secretion (GSIS), emphasising the role of beta cell dysfunction in the early stages of the disease. In search of novel mechanisms of beta cell dysfunction after long-term exposure to mild to severe glucotoxic conditions, we extensively characterised the alterations in insulin secretion and upstream coupling events in human islets cultured for 1–3 weeks at ~5, 8, 10 or 20 mmol/l glucose and subsequently stimulated by an acute stepwise increase in glucose concentration. Methods: Human islets from 49 non-diabetic donors (ND-islets) and six type 2 diabetic donors (T2D-islets) were obtained from five isolation centres. After shipment, the islets were precultured for 3–7 days in RPMI medium containing ~5 mmol/l glucose and 10% (vol/vol) heat-inactivated FBS with selective islet picking at each medium renewal. Islets were then cultured for 1–3 weeks in RPMI containing ~5, 8, 10 or 20 mmol/l glucose before measurement of insulin secretion during culture, islet insulin and DNA content, beta cell apoptosis and cytosolic and mitochondrial glutathione redox state, and assessment of dynamic insulin secretion and upstream coupling events during acute stepwise stimulation with glucose [NAD(P)H autofluorescence, ATP/(ATP+ADP) ratio, electrical activity, cytosolic Ca2+ concentration ([Ca2+]c)]. Results: Culture of ND-islets for 1–3 weeks at 8, 10 or 20 vs 5 mmol/l glucose did not significantly increase beta cell apoptosis or oxidative stress but decreased insulin content in a concentration-dependent manner and increased beta cell sensitivity to subsequent acute stimulation with glucose. Islet glucose responsiveness was higher after culture at 8 or 10 vs 5 mmol/l glucose and markedly reduced after culture at 20 vs 5 mmol/l glucose. In addition, the [Ca2+]c and insulin secretion responses to acute stepwise stimulation with glucose were
- Published
- 2022
13. In depth functional characterization of human induced pluripotent stem cell-derived beta cells in vitro and in vivo
- Author
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Fantuzzi, Federica, Toivonen, Sanna, Schiavo, Andréa Alex, Chae, Heedong, Tariq, Mohammad, Sawatani, Toshiaki, Pachera, Nathalie, Cai, Ying, Vinci, Chiara, Virgilio, Enrico, Ladrière, Laurence, Suleiman, Mara, Marchetti, Piero, Jonas, Jean-Christophe JJC, Gilon, Patrick, Eizirik, Décio L, Igoillo Esteve, Mariana, Cnop, Miriam, Fantuzzi, Federica, Toivonen, Sanna, Schiavo, Andréa Alex, Chae, Heedong, Tariq, Mohammad, Sawatani, Toshiaki, Pachera, Nathalie, Cai, Ying, Vinci, Chiara, Virgilio, Enrico, Ladrière, Laurence, Suleiman, Mara, Marchetti, Piero, Jonas, Jean-Christophe JJC, Gilon, Patrick, Eizirik, Décio L, Igoillo Esteve, Mariana, and Cnop, Miriam
- Abstract
In vitro differentiation of human induced pluripotent stem cells (iPSCs) into beta cells represents an important cell source for diabetes research. Here, we fully characterized iPSC-derived beta cell function in vitro and in vivo in humanized mice. Using a 7-stage protocol, human iPSCs were differentiated into islet-like aggregates with a yield of insulin-positive beta cells comparable to that of human islets. The last three stages of differentiation were conducted with two different 3D culture systems, rotating suspension or static microwells. In the latter, homogeneously small-sized islet-like aggregates were obtained, while in rotating suspension size was heterogeneous and aggregates often clumped. In vitro function was assessed by glucose-stimulated insulin secretion, NAD(P)H and calcium fluctuations. Stage 7 aggregates slightly increased insulin release in response to glucose in vitro .Aggregates were transplanted under the kidney capsule of NOD-SCID mice to allow for further in vivo beta cell maturation. In transplanted mice, grafts showed glucose-responsiveness and maintained normoglycemia after streptozotocin injection. In situ kidney perfusion assays showed modulation of human insulin secretion in response to different secretagogues. In conclusion, iPSCs differentiated with equal efficiency into beta cells in microwells compared to rotating suspension, but the former had a higher experimental success rate. In vitro differentiation generated aggregates lacking fully mature beta cell function. In vivo ,beta cells acquired the functional characteristics typical of human islets. With this technology an unlimited supply of islet-like organoids can be generated from human iPSCs that will be instrumental to study beta cell biology and dysfunction in diabetes., SCOPUS: ar.j, info:eu-repo/semantics/published
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- 2022
14. Identification of a human-specific alteration of beta cell function after prolonged culture of pancreatic islets under glucotoxic conditions
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Tariq, Mohammad, De Souza, Arnaldo Henrique, Chae, Hee-Young, Jaffredo, Manon, Wojtusciszyn, Anne, Raoux, Matthieu, Gilon, Patrick, Broca, Christophe, Jonas, Jean-Christophe, and UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition
- Abstract
Background and aims: The rapid reversibility of recent type 2 diabetes (T2D) by very low-calorie diet in some patients correlates with a marked improvement of glucose-stimulated insulin secretion (GSIS), emphasizing the role of β-cell dysfunction in the early stages of the disease. In search of human-specific mechanisms of β-cell dysfunction, we extensively characterized the glucotoxic alterations of insulin secretion and upstream coupling events in human pancreatic islets cultured for 1 to 3 weeks at ~5, 8, 10 or 20 mmol/l glucose and acutely stimulated by a stepwise increase in glucose concentration. Materials and methods: Islets from 46 non-diabetic (ND) and 6 type 2 diabetic (T2D) donors were obtained from 5 isolation centers over the last 10 years. The islets were precultured 3-7 days in RPMI containing 5 mmol/l glucose and 10% FBS. They were then cultured for 1-3 weeks in the same medium containing 5.5, 8.5, 10.5 or 20.5 mmol/l glucose before measurements of insulin secretion during culture, islet insulin/DNA content ratio, β-cell apoptosis, cytosolic and mitochondrial thiol redox state, and assessment of dynamic insulin secretion and upstream coupling events during stepwise stimulation with glucose (NAD(P)H autofluorescence, ATP/(ATP+ADP) ratio, electrical activity, cytosolic Ca2+ concentration ([Ca2+]c)). Results: Culture of ND-islets for 1 to 3 weeks at ~8, 10 or 20 vs 5 mmol/l glucose did not increase β-cell apoptosis or oxidative stress but concentration-dependently decreased insulin content and increased the β-cell sensitivity to subsequent stimulation with glucose. The islet glucose responsiveness (max amplitude of GSIS per islet) was larger after culture at 8 or 10 vs 5 mmol/l glucose but was markedly reduced after culture at 20 vs 5 mmol/l glucose. In the latter islets, [Ca2+]c and insulin secretion responses to acute stepwise stimulation with glucose were bell-shaped, with a maximal stimulation at 5 to 10 mmol/l glucose followed by a rapid sustained inhibition above that concentration. This glucotoxic alteration was a robust characteristic of human islets. It resulted from long-term stimulation of glucose metabolism and was fully reversible after culture at 5 mmol/l glucose. Finally, acute activation/inhibition of glucokinase during perifusion of islets cultured at 20 mmol/l glucose indicated that the acute reduction of [Ca2+]c and insulin secretion above 10 mmol/l glucose was due to overstimulation rather than inhibition of glucose metabolism. Similar results were obtained in islets from T2D-donors. Conclusion: Long-term exposure of human islets to mildly elevated glucose concentrations markedly increases their glucose sensitivity and reveals a bell-shaped glucose response curve for changes in [Ca2+]c and insulin secretion. This human-specific glucotoxic alteration may contribute to β-cell dysfunction in T2D independently from a detectable increase in β-cell apoptosis and oxidative stress.
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- 2022
15. Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreichʼs ataxia
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Igoillo-Esteve, Mariana, Gurgul-Convey, Ewa, Hu, Amélie, Romagueira Bichara Dos Santos, Laila, Abdulkarim, Baroj, Chintawar, Satyan, Marselli, Lorella, Marchetti, Piero, Jonas, Jean-Christophe, Eizirik, Décio L., Pandolfo, Massimo, and Cnop, Miriam
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- 2015
- Full Text
- View/download PDF
16. Transcriptome analysis of islets from diabetes‐resistant and diabetes‐prone obese mice reveals novel gene regulatory networks involved in beta‐cell compensation and failure
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Chan, Jeng Yie, primary, Bensellam, Mohammed, additional, Lin, Ruby C. Y., additional, Liang, Cassandra, additional, Lee, Kailun, additional, Jonas, Jean‐Christophe, additional, and Laybutt, D. Ross, additional
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- 2021
- Full Text
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17. Dual EPR measurement of oxygen consumption and superoxide production : principle and applications
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UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - Faculté de pharmacie et des sciences biomédicales, Gallez, Bernard, Jordan, Bénédicte, Sonveaux, Pierre, Feron, Olivier, Jonas, Jean-Christophe, Hardy, Micael, Mouithys-Mickalad, Ange, d'Hose, Donatienne, UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - Faculté de pharmacie et des sciences biomédicales, Gallez, Bernard, Jordan, Bénédicte, Sonveaux, Pierre, Feron, Olivier, Jonas, Jean-Christophe, Hardy, Micael, Mouithys-Mickalad, Ange, and d'Hose, Donatienne
- Abstract
A growing body of evidence indicates that mitochondria play a key role in many disorders as well as in cancer progression and response to treatment. Next to being the main cellular energy generator through respiration, mitochondria are also the major producer of superoxide and other downstream reactive oxygen species in the cell. In this thesis, we aimed to develop an integrated electron paramagnetic resonance (EPR) toolbox enabling the assessment of mitochondrial (dys)function by measuring the oxygen consumption rate and superoxide production in a same cellular or mitochondrial preparation. This EPR toolbox was used for the benefit of two different projects: discovering potential radiosensitizers in anticancer therapy (like statins) and assessing the impact of agents such as Boscalid and Bixafen, which are succinate dehydrogenase inhibitors (SDHI), on the mitochondrial function of human cells., (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2021
- Published
- 2021
18. Emerging Roles of Metallothioneins in Beta Cell Pathophysiology: Beyond and above Metal Homeostasis and Antioxidant Response
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UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, Bensellam, Mohammed, Laybutt, D. Ross, Jonas, Jean-Christophe, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, Bensellam, Mohammed, Laybutt, D. Ross, and Jonas, Jean-Christophe
- Abstract
Metallothioneins (MTs) are low molecular weight, cysteine-rich, metal-binding proteins whose precise biological roles have not been fully characterized. Existing evidence implicated MTs in heavy metal detoxification, metal ion homeostasis and antioxidant defense. MTs were thus categorized as protective effectors that contribute to cellular homeostasis and survival. This view has, however, been challenged by emerging evidence in different medical fields revealing novel pathophysiological roles of MTs, including inflammatory bowel disease, neurodegenerative disorders, carcinogenesis and diabetes. In the present focused review, we discuss the evidence for the role of MTs in pancreatic beta-cell biology and insulin secretion. We highlight the pattern of specific isoforms of MT gene expression in rodents and human beta-cells. We then discuss the mechanisms involved in the regulation of MTs in islets under physiological and pathological conditions, particularly type 2 diabetes, and analyze the evidence revealing adaptive and negative roles of MTs in beta-cells and the potential mechanisms involved. Finally, we underscore the unsettled questions in the field and propose some future research directions.
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- 2021
19. Transcriptome analysis of islets from diabetes-resistant and diabetes-prone obese mice reveals novel gene regulatory networks involved in beta cell compensation and failure.
- Author
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Chan JY, Bensellam M, Lin RCY, Liang C, Lee K, Jonas, Jean-Christophe, Laybutt DR, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Chan JY, Bensellam M, Lin RCY, Liang C, Lee K, Jonas, Jean-Christophe, and Laybutt DR
- Abstract
The mechanisms underpinning beta cell compensation for obesity-associated insulin resistance and beta cell failure in type 2 diabetes remain poorly understood. We used a large-scale strategy to determine the time-dependent transcriptomic changes in islets of diabetes-prone db/db and diabetes-resistant ob/ob mice at 6 and 16 weeks of age. Differentially expressed genes were subjected to cluster, gene ontology, pathway and gene set enrichment analyses. A distinctive gene expression pattern was observed in 16 wk db/db islets in comparison to the other groups with alterations in transcriptional regulators of islet cell identity, upregulation of glucose/lipid metabolism and various stress response genes, and downregulation of specific amino acid transport and metabolism genes. In contrast, ob/ob islets displayed a coordinated downregulation of metabolic and stress response genes at 6 weeks of age, suggestive of a preemptive reconfiguration in these islets to lower the threshold of metabolic activation in response to increased insulin demand thereby preserving beta cell function and preventing cellular stress. In addition, amino acid transport and metabolism genes were upregulated in ob/ob islets, suggesting an important role of glutamate metabolism in beta cell compensation. Gene set enrichment analysis of differentially expressed genes identified enrichment of binding motifs for transcription factors, FOXO4, NFATC1 and MAZ. siRNA-mediated knockdown of these genes in MIN6 cells altered cell death, insulin secretion and stress gene expression. In conclusion, these data revealed novel gene regulatory networks involved in beta cell compensation and failure. Preemptive metabolic reconfiguration in diabetes-resistant islets may dampen metabolic activation and cellular stress during obesity.
- Published
- 2021
20. The lack of functional nicotinamide nucleotide transhydrogenase only moderately contributes to the impairment of glucose tolerance and glucose-stimulated insulin secretion in C57BL/6J vs C57BL/6N mice.
- Author
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Close, Anne-Françoise, Chae, Heeyoung, Jonas, Jean-Christophe, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Close, Anne-Françoise, Chae, Heeyoung, and Jonas, Jean-Christophe
- Abstract
Aims/hypothesis: Nicotinamide nucleotide transhydrogenase (NNT) is involved in mitochondrial NADPH production and its spontaneous inactivating mutation (NntTr [Tr, truncated]) is usually considered to be the main cause of the lower glucose tolerance of C57BL/6J vs C57BL/6N mice. However, the impact of this mutation on glucose tolerance remains disputed. Here, we singled out the impact of NntTr from that of other genetic variants between C57BL/6J and C57BL/6N mice on mitochondrial glutathione redox state (EGSH), glucose-stimulated insulin secretion (GSIS) and glucose tolerance. Methods: Male and female N5BL/6J mice that express wild-type Nnt (NntWT) or NntTr (N5-WT and N5-Tr mice) on the C57BL/6J genetic background were obtained by crossing N5BL/6J NntWT/Tr heterozygous mice. C57BL/6J and C57BL/6N mice were from Janvier Labs. The Nnt genotype was confirmed by PCR and the genetic background by whole genome sequencing of one mouse of each type. Glucose tolerance was assessed by IPGTT, ITT and fasting/refeeding tests. Stimulus-secretion coupling events and GSIS were measured in isolated pancreatic islets. Cytosolic and mitochondrial EGSH were measured using the fluorescent redox probe GRX1-roGFP2 (glutaredoxin 1 fused to redox-sensitive enhanced GFP). Results: The Nnt genotype and genetic background of each type of mouse were confirmed. As reported previously in C57BL/6N vs C57BL/6J islets, the glucose regulation of mitochondrial (but not cytosolic) EGSH and of NAD(P)H autofluorescence was markedly improved in N5-WT vs N5-Tr islets, confirming the role of NNT in mitochondrial redox regulation. However, ex vivo GSIS was only 1.2-1.4-times higher in N5-WT vs N5-Tr islets, while it was 2.4-times larger in C57BL/6N vs N5-WT islets, questioning the role of NNT in GSIS. In vivo, the ITT results did not differ between N5-WT and N5-Tr or C57BL/6N mice. However, the glucose excursion during an IPGTT was only 15-20% lower in female N5-WT mice than in N5-Tr and C57BL/6J mice and r
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- 2021
21. Non-canonical mitochondrial STAT3 signaling mediates exercise-induced insulin secretion down-regulation
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Leite, Nayara C., primary, de Paula, Flávia, additional, Lubaczeuski, Camila, additional, Borck, Patricia C., additional, Juan-Mateu, Jonàs, additional, Souza, Jane C., additional, Eizirik, Decio L., additional, Boschero, Antonio C., additional, Jonas, Jean-Christophe, additional, Carneiro, Everardo M., additional, and Zoppi, Claudio C., additional
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- 2021
- Full Text
- View/download PDF
22. Emerging Roles of Metallothioneins in Beta Cell Pathophysiology: Beyond and above Metal Homeostasis and Antioxidant Response
- Author
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Bensellam, Mohammed, primary, Laybutt, D. Ross, additional, and Jonas, Jean-Christophe, additional
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- 2021
- Full Text
- View/download PDF
23. Inhibition of aquaporin-1 prevents myocardial remodeling by blocking the transmembrane transport of hydrogen peroxide
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Montiel, Virginie, Bella, Ramona, Michel, Lauriane Y. M., Esfahani, Hrag, De Mulder, Delphine, Robinson, Emma L., Deglasse, Jean-Philippe, Tiburcy, Malte, Chow, Pak Hin, Jonas, Jean-Christophe JJC, Gilon, Patrick, Steinhorn, Benjamin, Michel, Thomas, Beauloye, Christophe, Bertrand, Luc, Farah, Charlotte, Dei Zotti, Flavia, Debaix, Huguette, Bouzin, Caroline, Brusa, Davide, Horman, Sandrine, Vanoverschelde, Jean-Louis, Bergmann, Olaf, Gilis, Dimitri, Rooman, Marianne, Ghigo, Alessandra, Geninatti-Crich, Simonetta, Yool, Andrea, Zimmermann, Wolfram, Roderick, Llewelyn, Devuyst, Olivier, Balligand, Jean Luc, Montiel, Virginie, Bella, Ramona, Michel, Lauriane Y. M., Esfahani, Hrag, De Mulder, Delphine, Robinson, Emma L., Deglasse, Jean-Philippe, Tiburcy, Malte, Chow, Pak Hin, Jonas, Jean-Christophe JJC, Gilon, Patrick, Steinhorn, Benjamin, Michel, Thomas, Beauloye, Christophe, Bertrand, Luc, Farah, Charlotte, Dei Zotti, Flavia, Debaix, Huguette, Bouzin, Caroline, Brusa, Davide, Horman, Sandrine, Vanoverschelde, Jean-Louis, Bergmann, Olaf, Gilis, Dimitri, Rooman, Marianne, Ghigo, Alessandra, Geninatti-Crich, Simonetta, Yool, Andrea, Zimmermann, Wolfram, Roderick, Llewelyn, Devuyst, Olivier, and Balligand, Jean Luc
- Abstract
Pathological remodeling of the myocardium has long been known to involve oxidant signaling, but strategies using systemic antioxidants have generally failed to prevent it. We sought to identify key regulators of oxidant-mediated cardiac hypertrophy amenable to targeted pharmacological therapy. Specific isoforms of the aquaporin water channels have been implicated in oxidant sensing, but their role in heart muscle is unknown. RNA sequencing from human cardiac myocytes revealed that the archetypal AQP1 is a major isoform. AQP1 expression correlates with the severity of hypertrophic remodeling in patients with aortic stenosis. The AQP1 channel was detected at the plasma membrane of human and mouse cardiac myocytes from hypertrophic hearts, where it colocalized with NADPH oxidase-2 and caveolin-3. We show that hydrogen peroxide (H 2 O 2 ), produced extracellularly, is necessary for the hypertrophic response of isolated cardiac myocytes and that AQP1 facilitates the transmembrane transport of H 2 O 2 through its water pore, resulting in activation of oxidant-sensitive kinases in cardiac myocytes. Structural analysis of the amino acid residues lining the water pore of AQP1 supports its permeation by H 2 O 2 .Deletion of Aqp1 or selective blockade of the AQP1 intrasubunit pore inhibited H 2 O 2 transport in mouse and human cells and rescued the myocyte hypertrophy in human induced pluripotent stem cell–derived engineered heart muscle. Treatment of mice with a clinically approved AQP1 inhibitor, Bacopaside, attenuated cardiac hypertrophy. We conclude that cardiac hypertrophy is mediated by the transmembrane transport of H 2 O 2 by the water channel AQP1 and that inhibitors of AQP1 represent new possibilities for treating hypertrophic cardiomyopathies., info:eu-repo/semantics/published
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- 2020
24. Inhibition of aquaporin-1 prevents myocardial remodeling by blocking the transmembrane transport of hydrogen peroxide
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Montiel, Virginie, primary, Bella, Ramona, additional, Michel, Lauriane Y. M., additional, Esfahani, Hrag, additional, De Mulder, Delphine, additional, Robinson, Emma L., additional, Deglasse, Jean-Philippe, additional, Tiburcy, Malte, additional, Chow, Pak Hin, additional, Jonas, Jean-Christophe, additional, Gilon, Patrick, additional, Steinhorn, Benjamin, additional, Michel, Thomas, additional, Beauloye, Christophe, additional, Bertrand, Luc, additional, Farah, Charlotte, additional, Dei Zotti, Flavia, additional, Debaix, Huguette, additional, Bouzin, Caroline, additional, Brusa, Davide, additional, Horman, Sandrine, additional, Vanoverschelde, Jean-Louis, additional, Bergmann, Olaf, additional, Gilis, Dimitri, additional, Rooman, Marianne, additional, Ghigo, Alessandra, additional, Geninatti-Crich, Simonetta, additional, Yool, Andrea, additional, Zimmermann, Wolfram H., additional, Roderick, H. Llewelyn, additional, Devuyst, Olivier, additional, and Balligand, Jean-Luc, additional
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- 2020
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25. Editorial Overview: “Islet Biology in Type 2 Diabetes”
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Gaisano, Herbert Y., primary, Jonas, Jean-Christophe, additional, and Gloyn, Anna L., additional
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- 2020
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26. Nutrient Metabolism, Subcellular Redox State, and Oxidative Stress in Pancreatic Islets and β-Cells
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Roma, Leticia P., primary and Jonas, Jean-Christophe, additional
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- 2020
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27. Aspalathin Protects Insulin‐Producing β Cells against Glucotoxicity and Oxidative Stress‐Induced Cell Death
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Moens, Céline, primary, Bensellam, Mohammed, additional, Himpe, Eddy, additional, Muller, Christo J. F., additional, Jonas, Jean‐Christophe, additional, and Bouwens, Luc, additional
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- 2020
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28. Exenatide induces frataxin expression and improves mitochondrial function in Friedreich ataxia
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Igoillo-Esteve, Mariana, primary, Oliveira, Ana F., additional, Cosentino, Cristina, additional, Fantuzzi, Federica, additional, Demarez, Céline, additional, Toivonen, Sanna, additional, Hu, Amélie, additional, Chintawar, Satyan, additional, Lopes, Miguel, additional, Pachera, Nathalie, additional, Cai, Ying, additional, Abdulkarim, Baroj, additional, Rai, Myriam, additional, Marselli, Lorella, additional, Marchetti, Piero, additional, Tariq, Mohammad, additional, Jonas, Jean-Christophe, additional, Boscolo, Marina, additional, Pandolfo, Massimo, additional, Eizirik, Décio L., additional, and Cnop, Miriam, additional
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- 2020
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- View/download PDF
29. Proof-of-concept for 2D/CT element analysis of entire cryofrozen islets of Langerhans using a cryoloop synchrotron X-ray fluorescence setup
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De Samber, Björn, primary, Bensellam, Mohammed, additional, Van Malderen, Stijn J. M., additional, Seiboth, Frank, additional, Brückner, Dennis, additional, Garrevoet, Jan, additional, Falkenberg, Gerald, additional, Jonas, Jean-Christophe, additional, and Vincze, Laszlo, additional
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- 2020
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30. Exenatide induces frataxin expression and improves mitochondrial function in Friedreich ataxia.
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Igoillo Esteve, Mariana, Martins Oliveira, Ana Filipa, Cosentino, Cristina, Fantuzzi, Federica, Demarez, Céline, Toivonen, Sanna, Hu, Amelie, Chintawar, Satyan, Lopes, Miguel, Pachera, Nathalie, Cai, Ying, Abdulkarim, Baroj, Rai, Myriam, Marselli, Lorella, Marchetti, Piero, Tariq, Mohammad, Jonas, Jean-Christophe JJC, Boscolo, Marina, Pandolfo, Massimo, Eizirik, Decio L., Cnop, Miriam, Igoillo Esteve, Mariana, Martins Oliveira, Ana Filipa, Cosentino, Cristina, Fantuzzi, Federica, Demarez, Céline, Toivonen, Sanna, Hu, Amelie, Chintawar, Satyan, Lopes, Miguel, Pachera, Nathalie, Cai, Ying, Abdulkarim, Baroj, Rai, Myriam, Marselli, Lorella, Marchetti, Piero, Tariq, Mohammad, Jonas, Jean-Christophe JJC, Boscolo, Marina, Pandolfo, Massimo, Eizirik, Decio L., and Cnop, Miriam
- Abstract
Friedreich ataxia is an autosomal recessive neurodegenerative disease associated with a high diabetes prevalence. No treatment is available to prevent or delay disease progression. Friedreich ataxia is caused by intronic GAA trinucleotide repeat expansions in the frataxin-encoding FXN gene that reduce frataxin expression, impair iron-sulfur cluster biogenesis, cause oxidative stress, and result in mitochondrial dysfunction and apoptosis. Here we examined the metabolic, neuroprotective and frataxin-inducing effects of glucagon-like-peptide 1 (GLP-1) analogs in in vivo and in vitro models and in Friedreich ataxia patients. The GLP-1 analog exenatide improved glucose homeostasis of frataxin-deficient mice through enhanced insulin content and secretion in pancreatic β-cells. Exenatide induced frataxin and iron-sulfur cluster-containing proteins in β-cells and brain, and was protective to sensory neurons in dorsal root ganglia. GLP-1 analogs also induced frataxin expression, reduced oxidative stress and improved mitochondrial function in Friedreich ataxia patients' induced pluripotent stem cell-derived β-cells and sensory neurons. The frataxin-inducing effect of exenatide was confirmed in a pilot trial in Friedreich ataxia patients, showing modest frataxin induction in platelets over a 5-week treatment course. Taken together, GLP-1 analogs improve mitochondrial function in frataxin-deficient cells and induce frataxin expression. Our findings identify incretin receptors as a therapeutic target in Friedreich ataxia., info:eu-repo/semantics/published
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- 2019
31. Targeting soluble 5’-nucleotidases NT5C1A and NT5C2 as a strategy for AMPK activation
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UCL - SSS/DDUV/PHOS - Protein phosphorylation, UCL - Faculté de pharmacie et des sciences biomédicales, Rider, Mark, Leclercq, Isabelle, Jonas, Jean-Christophe, Cani, Patrice, Bertrand, Luc, Sakamoto, Kei, Kviklyte, Samanta, UCL - SSS/DDUV/PHOS - Protein phosphorylation, UCL - Faculté de pharmacie et des sciences biomédicales, Rider, Mark, Leclercq, Isabelle, Jonas, Jean-Christophe, Cani, Patrice, Bertrand, Luc, Sakamoto, Kei, and Kviklyte, Samanta
- Abstract
AMP-activated protein kinase (AMPK) is a key player in the control of cellular energy homeostasis. AMPK activation is associated with beneficial effects to counteract the metabolic syndrome, and AMPK is now recognized as a potential drug target for the treatment of type 2 diabetes. However, research findings have been controversial. The aim of the thesis was to understand whether genetic deletion of AMP-metabolizing enzymes would be a viable approach to achieve AMPK activation and whether enzyme inhibition could be a pharmacological strategy for the treatment of type 2 diabetes. The first part of the thesis focused on the effects of cytosolic 5`-nucleotidase 1A (NT5C1A) and of cytosolic 5`-nucleotidase II (NT5C2) deletion in incubated skeletal muscles. The second part focused on whether NT5C2 deletion could improve glycaemic control in mice fed normal and high fat diet in comparison to wild-type mice., La protéine kinase activée par l'AMP (AMPK) est impliquée dans le contrôle de l’homéostasie énergétique cellulaire. Son activation a des effets bénéfiques pour contrecarrer le syndrome métabolique et l'AMPK est reconnue comme cible potentielle pour le traitement du diabète de type 2. Cependant, les résultats actuels de la recherche font débat. Cette thèse visait à évaluer si la délétion génétique des enzymes métabolisant l’AMP constitue une approche valable pour activer l’AMPK et si l’inhibition de cette dernière pouvait servir de stratégie pharmacologique pour le traitement du diabète de type 2. La première partie de l’étude s’est concentrée sur les effets liés aux délétions des 5`-nucleotidase 1A (NT5C1A) et 5`-nucleotidase II (NT5C2) cytosoliques dans les muscles squelettiques incubés. La seconde a investigué si la délétion de NT5C2 améliore le contrôle de la glycémie chez des souris soumises à un régime normal ou riche en graisse, en comparaison à des souris de type sauvage., (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2019
- Published
- 2019
32. Metallothionein 1 negatively regulates glucose-stimulated insulin secretion and is differentially expressed in conditions of beta cell compensation and failure in mice and humans
- Author
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Bensellam, Mohammed, Shi, Yan-Chuan, Chan, Jeng Yie, Laybutt, D. Ross, Chae, Heeyoung, Abou Samra, Michel, Pappas, Evan G., Thomas, Helen E., Gilon, Patrick, Jonas, Jean-Christophe, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Bensellam, Mohammed, Shi, Yan-Chuan, Chan, Jeng Yie, Laybutt, D. Ross, Chae, Heeyoung, Abou Samra, Michel, Pappas, Evan G., Thomas, Helen E., Gilon, Patrick, and Jonas, Jean-Christophe
- Abstract
Aims/hypothesis: The mechanisms responsible for beta cell compensation in obesity and for beta cell failure in type 2 diabetes are poorly defined. The mRNA levels of several metallothionein (MT) genes are upregulated in islets from individuals with type 2 diabetes, but their role in beta cells is not clear. Here we examined: 1) the temporal changes of islet Mt1 and Mt2 gene expression in mouse models of beta cell compensation and failure; and 2) the role of Mt1 and Mt2 in beta cell function and glucose homeostasis in mice. Methods: Mt1 and Mt2 expression was assessed in islets from: (1) control lean (chow diet-fed) and diet-induced obese (high-fat diet-fed for 6 weeks) mice; (2) mouse models of prediabetes (6-week-old db/db mice) and diabetes (16-week-old db/db mice) and age-matched db/+ (control) mice; and (3) obese non-diabetic ob/ob mice (16-week-old) and age-matched ob/+ (control) mice. MT1E, MT1X and MT2A expression was assessed in islets from humans with and without type 2 diabetes. Mt1-Mt2 double-knockout (KO) mice, transgenic mice overexpressing Mt1 under the control of its natural promoter (Tg-Mt1) and corresponding control mice were also studied. In MIN6 cells, MT1 and MT2 were inhibited by small interfering RNAs. mRNA levels were assessed by real-time RT-PCR, plasma insulin and islet MT levels by ELISA, glucose tolerance by i.p. glucose tolerance tests and fasting 1 h refeeding tests, insulin tolerance by i.p. insulin tolerance tests, insulin secretion by RIA, cytosolic free Ca2+ concentration with Fura-2 leakage resistant (Fura-2 LR), cytosolic free Zn2+ concentration with Fluozin-3, and NAD(P)H by autofluorescence. Results: Mt1 and Mt2 mRNA levels were reduced in islets of murine models of beta cell compensation, whereas they were increased in diabetic db/db mice. In humans, MT1X mRNA levels were significantly upregulated in islets from individuals with type 2 diabetes in comparison with non-diabetic donors, while MT1E and MT2A mRNA levels were unchange
- Published
- 2019
33. Anticancer photodynamic therapy from direct cytotoxic effects to immunogenic cell death induction
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UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - Faculté de pharmacie et des sciences biomédicales, Feron, Olivier, Jonas, Jean-Christophe, Machiels, Jean-Pascal, Coulie, Pierre, Michiels, Carine, Agostinis, Patrizia, Vooijs, Marc, Doix, Bastien, UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - Faculté de pharmacie et des sciences biomédicales, Feron, Olivier, Jonas, Jean-Christophe, Machiels, Jean-Pascal, Coulie, Pierre, Michiels, Carine, Agostinis, Patrizia, Vooijs, Marc, and Doix, Bastien
- Abstract
Photodynamic therapy (PDT) is a medical treatment aimed at destroying pathological tissues including (pre-)cancerous lesions using photosensitizers (PS). Exposure of these compounds to light (often from a laser) induces local cytotoxicity following the photochemical production of singlet oxygen and reactive oxygen species. The induction of immunogenic cell death by PDT has recently suggested its potential use in cancer immunotherapy. OR141 is the lead compound of a family of benzophenazine-type PS discovered at UCLouvain. Here, we explored the direct anticancer effects of OR141 and its ability to stimulate the immune system, including through the optimization of a dendritic cell-based antitumor vaccine. This research has demonstrated the possibility of using white light to activate this PS, considerably broadening its spectrum of use. Our work also revealed the value of a submaximal dose of PS to promote the host's immune response and the existence of an optimal timing of PDT delivery when combined with radiotherapy., La thérapie photodynamique (PDT) est un traitement médical visant à détruire des tissus pathologiques dont des lésions (pré-)cancéreuses à l’aide de photosensibilisateurs (PS). L’exposition à la lumière (souvent d’un laser) de ces composés induit une cytotoxicité locale suite à la production photochimique d’oxygène singulet et d’espèces réactives de l’oxygène. L’induction d’une mort cellulaire de type immunogénique par la PDT a récemment suggéré son utilisation potentielle dans l’immunothérapie du cancer. OR141 est le chef de file d’une famille de PS découverts à l’UCLouvain. Nous avons exploré les effets anticancéreux directs d’OR141 et sa capacité à stimuler le système immunitaire, ce compris via l’optimisation d’un vaccin antitumoral à base de cellules dendritiques. Ces recherches ont démontré la possibilité d’utiliser une lumière blanche pour activer ce PS, élargissant considérablement son spectre d’utilisation. Notre travail a également révélé l’intérêt d’une dose submaximale de PS pour favoriser la réponse immunitaire de l’hôte ainsi que l’existence d’un timing optimal de délivrance de la PDT lorsque combinée à la radiothérapie., (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2019
- Published
- 2019
34. Transcriptome analysis of islets from diabetes-resistant and diabetes-prone obese mice reveals novel gene regulatory networks involved in beta-cell compensation and failure.
- Author
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Jeng Yie Chan, Bensellam, Mohammed, Lin, Ruby C. Y., Liang, Cassandra, Lee, Kailun, Jonas, Jean-Christophe, and Laybutt, D. Ross
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- 2021
- Full Text
- View/download PDF
35. Metallothionein 1 inhibits glucose-stimulated insulin secretion and is differentially regulated in conditions of beta cell compensation and failure
- Author
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Bensellam, Mohammed, Shi, Yan-Chuan, Chan, Jeng Yie, Laybutt, D. Ross, Jonas, Jean-Christophe, 54th EASD Annual Meeting of the European Association for the Study of Diabetes, and UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition
- Subjects
beta cell compensation ,beta cell failure ,islets ,endocrine system ,obesity ,type 2 diabetes ,glucose-stimulated insulin secretion - Abstract
Background and aims: The mechanisms responsible for β cell compensation in obesity and for β cell failure in type 2 diabetes (T2D) are poorly defined. Metallothioneins play a role in both Zn2+ homeostasis and the regulation of cellular redox state. The mRNA levels of several metallothionein genes are upregulated in islets from subjects with T2D, but their role in β cells is not clear. Here we examined: 1) the temporal changes of islet Mt1 and Mt2 gene expression in models of β cell compensation and failure, and 2) the role of Mt1 and Mt2 in β cell function and glucose homeostasis. Materials and methods: Mt1 and Mt2 expression was assessed in islets from control lean (chow diet) and diet-induced obese (DIO) mice (8 weeks high fat diet), and pre-diabetic (6-week-old) and diabetic (16-week-old) db/db mice and age-matched db/+ (control) mice. Mt1-Mt2 double knockout (KO) mice, Mt1 overexpressing transgenic mice (Tg-Mt1) and corresponding control mice were studied. Mt1 and Mt2 were inhibited in MIN6 cells by small interfering RNAs. mRNA levels were assessed by real-time RT-PCR, plasma insulin and islet metallothionein levels by ELISA, glucose tolerance by i.p. glucose tolerance tests (ipGTT) and fasting-1h refeeding tests, insulin secretion by RIA, cytosolic free Ca2+ with Fura-2 LR, NAD(P)H by autofluorescence and cytosolic redox state using roGFP1 ratiometric thiol redox probe. Results: Increased plasma insulin levels (β cell compensation) correlated with marked downregulation of Mt1 and Mt2 mRNA levels in islets of DIO mice (Mt1: ~4-fold, p
- Published
- 2018
36. Glucose Acutely Reduces Cytosolic and Mitochondrial H2O2in Rat Pancreatic Beta Cells
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Deglasse, Jean-Philippe, primary, Roma, Leticia Prates, additional, Pastor-Flores, Daniel, additional, Gilon, Patrick, additional, Dick, Tobias P., additional, and Jonas, Jean-Christophe, additional
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- 2019
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37. Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes.
- Author
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Cosentino, Cristina, Toivonen, Sanna, Diaz Villamil, Esteban, Atta, Mohamed MA, Ravanat, Jean-Luc, Demine, Stéphane, Schiavo, Andréa Alex, Pachera, Nathalie, Deglasse, Jean-Philippe, Jonas, Jean-Christophe JJC, Balboa, Diego, Otonkoski, Timo, Pearson, Ewan ER, Marchetti, Piero, Eizirik, Decio L., Cnop, Miriam, Igoillo Esteve, Mariana, Cosentino, Cristina, Toivonen, Sanna, Diaz Villamil, Esteban, Atta, Mohamed MA, Ravanat, Jean-Luc, Demine, Stéphane, Schiavo, Andréa Alex, Pachera, Nathalie, Deglasse, Jean-Philippe, Jonas, Jean-Christophe JJC, Balboa, Diego, Otonkoski, Timo, Pearson, Ewan ER, Marchetti, Piero, Eizirik, Decio L., Cnop, Miriam, and Igoillo Esteve, Mariana
- Abstract
Transfer RNAs (tRNAs) are non-coding RNA molecules essential for protein synthesis. Post-transcriptionally they are heavily modified to improve their function, folding and stability. Intronic polymorphisms in CDKAL1, a tRNA methylthiotransferase, are associated with increased type 2 diabetes risk. Loss-of-function mutations in TRMT10A, a tRNA methyltransferase, are a monogenic cause of early onset diabetes and microcephaly. Here we confirm the role of TRMT10A as a guanosine 9 tRNA methyltransferase, and identify tRNAGln and tRNAiMeth as two of its targets. Using RNA interference and induced pluripotent stem cell-derived pancreatic β-like cells from healthy controls and TRMT10A-deficient patients we demonstrate that TRMT10A deficiency induces oxidative stress and triggers the intrinsic pathway of apoptosis in β-cells. We show that tRNA guanosine 9 hypomethylation leads to tRNAGln fragmentation and that 5'-tRNAGln fragments mediate TRMT10A deficiency-induced β-cell death. This study unmasks tRNA hypomethylation and fragmentation as a hitherto unknown mechanism of pancreatic β-cell demise relevant to monogenic and polygenic forms of diabetes., SCOPUS: ar.j, info:eu-repo/semantics/published
- Published
- 2018
38. Biomarkers of tumor redox status in response to modulations of glutathione and thioredoxin antioxidant pathways.
- Author
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UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Kengen, Julie, Deglasse, Jean-Philippe, Neveu, Marie-Aline, Mignion, Lionel, Desmet, Céline, Gourgue, Florian, Jonas, Jean-Christophe, Gallez, Bernard, Jordan, Bénédicte, UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Kengen, Julie, Deglasse, Jean-Philippe, Neveu, Marie-Aline, Mignion, Lionel, Desmet, Céline, Gourgue, Florian, Jonas, Jean-Christophe, Gallez, Bernard, and Jordan, Bénédicte
- Abstract
The ability of certain cancer cells to maintain a highly reduced intracellular environment is correlated with aggressiveness and drug resistance. Since the gluthathione (GSH) and thioredoxin (TRX) systems cooperate to a tight regulation of ROS in cell physiology, and to a stimulation of tumor initiation and progression, modulation of the GSH and TRX pathways are emerging as new potential targets in cancer. In vivo methods to assess changes in tumor redox status are critically needed to assess the relevance of redox-targeted agents. The current study assesses in vitro and in vivo biomarkers of tumor redox status in response to treatments targeting the GSH and TRX pathways, by comparing cytosolic and mitochondrial redox nitroxide Electron Paramagnetic Resonance (EPR) probes, and cross-validation with redox dynamic fluorescent measurement. For that purpose, the effect of the GSH modulator buthionine sulfoximine (BSO) and of the TRX reductase inhibitor auranofin were measured in vitro using both cytosolic and mitochondrial EPR and roGFP probes in breast and cervical cancer cells. In vivo, mice bearing breast or cervical cancer xenografts were treated with the GSH or TRX modulators and monitored using the mito-TEMPO spin probe. Our data highlight the importance of using mitochondria targeted spin probes to assess changes in tumor redox status induced by redox modulators. Further in vivo validation of the mito-tempo spin probe with alternative in vivo methods should be considered, yet the spin probe used in vivo in xenografts demonstrated sensitivity to the redox status modulators.
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- 2018
39. Glucolipotoxic conditions induce beta-cell iron import, cytosolic ROS formation and apoptosis
- Author
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UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Hansen, Jakob B, Dos Santos, Laila RB, Liu, Ying, Prentice, Kacey J, Teudt, Frederik, Tonnesen, Morten, Jonas, Jean-Christophe, Wheeler, Michael B, Mandrup-Poulsen, Thomas, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, Hansen, Jakob B, Dos Santos, Laila RB, Liu, Ying, Prentice, Kacey J, Teudt, Frederik, Tonnesen, Morten, Jonas, Jean-Christophe, Wheeler, Michael B, and Mandrup-Poulsen, Thomas
- Abstract
Type 2 diabetes (T2D) arises when the pancreatic beta-cell fails to compensate for increased insulin needs due to insulin resistance. Glucolipotoxicity has been proposed to induce beta-cell dysfunction in T2D by formation of reactive oxygen species (ROS). Here we examined if modelling glucolipotoxic conditions by high glucose-high free fatty acid (FFA) exposure (GLT) regulate beta-cell iron transport, thereby increasing the cytosolic labile iron pool and iron-catalyzed ROS formation. We show that GLT -induced ROS production is regulated by an increased labile iron pool (LIP) associated with elevated expression of genes regulating iron import. Using pharmacological and transgenic approaches, we show that iron reduction and decreased iron import protects from GLT-induced ROS production, prevents impairment of the mitochondrial membrane potential, and inhibits apoptosis. This study identifies a novel pathway underlying GLT-induced apoptosis involving increased iron import, generation of hydroxyl radicals from hydrogen peroxide through the Fenton reaction in the cytosolic compartment associated with dissipation of the mitochondrial membrane potential and beta cell apoptosis.
- Published
- 2018
40. Ovarian tissue cryopreservation and transplantation : angiogenesis enhancement in cryopreserved ovarian tissue grafts using adipose tissue-derived stem cells
- Author
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UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Dolmans, Marie-Madeleine, Jonas, Jean-Christophe, Amorim, Christiani Andrade, Jordan, Bénédicte, Marbaix, Etienne, Lysy, Philippe, Diaz-Garcia, César, Demeestere, Isabelle, Manavella Isasmendi, Diego Daniel, UCL - SSS/IREC/GYNE - Pôle de Gynécologie, UCL - Faculté de médecine et médecine dentaire, Dolmans, Marie-Madeleine, Jonas, Jean-Christophe, Amorim, Christiani Andrade, Jordan, Bénédicte, Marbaix, Etienne, Lysy, Philippe, Diaz-Garcia, César, Demeestere, Isabelle, and Manavella Isasmendi, Diego Daniel
- Abstract
Ovarian tissue cryopreservation and transplantation is the only way for prepubertal and young female cancer patients to preserve their fertility, but this promising technique (more than 130 births) still has limitations due to follicle loss post-grafting. Indeed, avascular grafts need 5 days to become revascularized, during which time >60% of follicles are lost. In this context, the aim of the present work was to identify a better transplantation technique to limit this follicular loss by stimulating early angiogenesis in ovarian tissue grafts using adipose tissue-derived stem cells (ASCs). This new technique involved a two-step transplantation procedure with (i) preparation of the grafting site and (ii) transplantation of ovarian fragments to the prepared site. A key question that was also addressed in the present work was the mechanism by which ASCs exert their proangiogenic effects in grafted ovarian tissue., La congélation et la transplantation du tissu ovarien est la seule possibilité pour les jeunes patientes prépubères de préserver leur fertilité avant traitement anti-cancéreux. Cette technique prometteuse (plus de 130 naissances) présente néanmoins encore des limitations dans son succès dû à la perte folliculaire post-greffe. En effet, la greffe avasculaire de fragments d’ovaire met 5 jours avant d’être revascularisée, temps pendant lequel >60% des follicules meurent. Dans ce contexte, le présent travail a comme but de trouver une meilleure technique de greffe ovarienne qui a fin de limiter cette perte folliculaire, en stimulant une angiogenèse précoce dans les greffons de tissu ovarien via des cellules souches adipeuses. Cette nouvelle technique consiste en une procédure de transplantation en deux étapes: (i) préparation du site de greffe et (ii) transplantation de tissu ovarien sur le site préparé. Le mécanisme par lequel les cellules souches exercent leurs effets pro-angiogéniques dans le tissu ovarien greffé est aussi analysé., (MED - Sciences médicales) -- UCL, 2018
- Published
- 2018
41. Glucolipotoxic conditions induce beta-cell iron import, cytosolic ROS formation and apoptosis
- Author
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Hansen, Jakob Bondo, Dos Santos, Laila Romagueira Bichara, Liu, Ying, Prentice, Kacey J., Teudt, Frederik, Tonnesen, Morten, Jonas, Jean-Christophe, Wheeler, Michael B., Mandrup-Poulsen, Thomas, Hansen, Jakob Bondo, Dos Santos, Laila Romagueira Bichara, Liu, Ying, Prentice, Kacey J., Teudt, Frederik, Tonnesen, Morten, Jonas, Jean-Christophe, Wheeler, Michael B., and Mandrup-Poulsen, Thomas
- Abstract
Type 2 diabetes (T2D) arises when the pancreatic beta-cell fails to compensate for increased insulin needs due to insulin resistance. Glucolipotoxicity (GLT) has been proposed to induce beta-cell dysfunction in T2D by formation of reactive oxygen species (ROS). Here, we examined if modeling glucolipotoxic conditions by high glucose-high free fatty acid (FFA) exposure (GLT) regulates beta-cell iron transport, by increasing the cytosolic labile iron pool (LIP). In isolated mouse islets, the GLT-induced increase in the LIP catalyzed cytosolic ROS formation and induced apoptosis. We show that GLT-induced ROS production is regulated by an increased LIP associated with elevated expression of genes regulating iron import. Using pharmacological and transgenic approaches, we show that iron reduction and decreased iron import protects from GLT-induced ROS production, prevents impairment of the mitochondrial membrane potential (MMP) and inhibits apoptosis. This study identifies a novel pathway underlying GLT-induced apoptosis involving increased iron import, generation of hydroxyl radicals from hydrogen peroxide through the Fenton reaction in the cytosolic compartment associated with dissipation of the MMP and beta-cell apoptosis.
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- 2018
42. Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes
- Author
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Cosentino, Cristina, primary, Toivonen, Sanna, additional, Diaz Villamil, Esteban, additional, Atta, Mohamed, additional, Ravanat, Jean-Luc, additional, Demine, Stéphane, additional, Schiavo, Andrea Alex, additional, Pachera, Nathalie, additional, Deglasse, Jean-Philippe, additional, Jonas, Jean-Christophe, additional, Balboa, Diego, additional, Otonkoski, Timo, additional, Pearson, Ewan R, additional, Marchetti, Piero, additional, Eizirik, Décio L, additional, Cnop, Miriam, additional, and Igoillo-Esteve, Mariana, additional
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- 2018
- Full Text
- View/download PDF
43. Somatostatin Is Only Partly Required for the Glucagonostatic Effect of Glucose but Is Necessary for the Glucagonostatic Effect of KATP Channel Blockers
- Author
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Lai, Bao-Khanh, primary, Chae, Heeyoung, additional, Gómez-Ruiz, Ana, additional, Cheng, Panpan, additional, Gallo, Paola, additional, Antoine, Nancy, additional, Beauloye, Christophe, additional, Jonas, Jean-Christophe, additional, Seghers, Victor, additional, Seino, Susumu, additional, and Gilon, Patrick, additional
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- 2018
- Full Text
- View/download PDF
44. Glucolipotoxic conditions induce β-cell iron import, cytosolic ROS formation and apoptosis
- Author
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Hansen, Jakob Bondo, primary, Dos Santos, Laila Romagueira Bichara, additional, Liu, Ying, additional, Prentice, Kacey J, additional, Teudt, Frederik, additional, Tonnesen, Morten, additional, Jonas, Jean-Christophe, additional, Wheeler, Michael B, additional, and Mandrup-Poulsen, Thomas, additional
- Published
- 2018
- Full Text
- View/download PDF
45. Mechanisms of β-cell dedifferentiation in diabetes: recent findings and future research directions
- Author
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Bensellam, Mohammed, primary, Jonas, Jean-Christophe, additional, and Laybutt, D Ross, additional
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- 2018
- Full Text
- View/download PDF
46. Biomarkers of tumour redox status in response to modulations of glutathione and thioredoxin antioxidant pathways
- Author
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Kengen, Julie, primary, Deglasse, Jean-Philippe, additional, Neveu, Marie-Aline, additional, Mignion, Lionel, additional, Desmet, Céline, additional, Gourgue, Florian, additional, Jonas, Jean-Christophe, additional, Gallez, Bernard, additional, and Jordan, Bénédicte F., additional
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- 2018
- Full Text
- View/download PDF
47. Functional characterization and imaging of oxidative lactate metabolism in cancer
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UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - Faculté de pharmacie et des sciences biomédicales, Sonveaux, Pierre, Delzenne, Nathalie, Jordan, Bénédicte, Jonas, Jean-Christophe, Grégoire, Vincent, Bormans, Guy, Baltazar, Fátima, Van Hee, Vincent, UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - Faculté de pharmacie et des sciences biomédicales, Sonveaux, Pierre, Delzenne, Nathalie, Jordan, Bénédicte, Jonas, Jean-Christophe, Grégoire, Vincent, Bormans, Guy, Baltazar, Fátima, and Van Hee, Vincent
- Abstract
Increasing evidence indicate that lactate, the end-product of a glycolytic metabolism, promotes tumor progression. In addition to being used as an oxidative fuel, lactate indeed stimulates angiogenesis by activating transcription factors HIF-1 in oxidative cancer cells and endothelial cells, and NF-kB in endothelial cells. Our work shows that lactate does not activate NF-kB in oxidative cancer cells, because NADH produced during its oxidation is used in mitochondria rather than fueling NAP(P)H oxidases. Thus, lactate influx inhibition can prevent the oxidative use of lactate in cancer. A main target is inward monocarboxylate transporter 1 (MCT1). We therefore developed a tracer of lactate for positron emission tomography that allows to predict and to document a response to MCT1 inhibitors in vivo. Together, our work contributes to a better understanding and therapeutic exploitation of lactate transport in cancer., (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2017
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- 2017
48. The role of activating transcription factor 3 in mouse skeletal muscle
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UCL - SSS/IONS - Institute of NeuroScience, UCL - Faculté des sciences de la motricité, Francaux , Marc, Lemaigre, Frédéric, Deldicque, Louise, Thonnard, Jean-Louis, Thissen, Jean-Paul, Jonas, Jean-Christophe, Pilegaard, Henriette, Demoulin, Jean-Baptiste, Fernandez Verdejo, Rodrigo, UCL - SSS/IONS - Institute of NeuroScience, UCL - Faculté des sciences de la motricité, Francaux , Marc, Lemaigre, Frédéric, Deldicque, Louise, Thonnard, Jean-Louis, Thissen, Jean-Paul, Jonas, Jean-Christophe, Pilegaard, Henriette, Demoulin, Jean-Baptiste, and Fernandez Verdejo, Rodrigo
- Abstract
Exercise has anti-inflammatory properties useful to prevent and treat some chronic diseases. The expression of activating transcription factor 3 (ATF3) increases in skeletal muscle after exercise. In many tissues, ATF3 regulates the inflammatory response. Whether ATF3 contributes to the anti-inflammatory properties of exercise in skeletal muscle was unknown. To understand the role of ATF3 in skeletal muscle, we used a mutant mouse model unable to express ATF3 (ATF3-KO). We found that the expression of some inflammation-related genes was higher in ATF3-KO than control mice postexercise. ATF3-KO mice also had an impaired molecular adaptation to training in skeletal muscle. Our data suggest ATF3 is an important regulator of the inflammation postexercise, which could influence training adaptation in skeletal muscle. Since inflammation is involved in the pathogenesis of many diseases, the identification of ATF3 as an exercise-induced anti-inflammatory factor is relevant for future studies., (MOTR - Sciences de la motricité) -- UCL, 2017
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- 2017
49. Dynamic changes of oxygenation in wound healing in mice diabetic models monitored by Electron Paramagnetic Resonance (EPR) oximetry
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UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - Faculté de pharmacie et des sciences biomédicales, Gallez, Bernard, Levêque, Philippe, Feron, Olivier, Jordan, Bénédicte, Jonas, Jean-Christophe, Vandeleene, Bernard, Germonpré, Peter, Frapart, Yves-Michel, Desmet, Céline, UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - Faculté de pharmacie et des sciences biomédicales, Gallez, Bernard, Levêque, Philippe, Feron, Olivier, Jordan, Bénédicte, Jonas, Jean-Christophe, Vandeleene, Bernard, Germonpré, Peter, Frapart, Yves-Michel, and Desmet, Céline
- Abstract
Oxygen is essential in wound healing and hypoxia is described as a major cause of wound healing impairment. Tissue oxygenation is an important parameter in the clinical management of chronic wounds such as diabetic ulcers. But until now, no techniques are able to perform absolute, non-invasive and repeated measurements of oxygenation directly in a tissue. Electron Paramagnetic Resonance (EPR) oximetry is a technique that allows this kind of measurements, but was never applied in the context of diabetic wound healing. The aim of the thesis was the implementation of EPR oximetry to follow diabetic wound oxygenation variations. The first part of the thesis consisted in the validation of the technique to measure wound oxygenation. Then, the use of EPR oximetry as a biomarker of treatment response in diabetic wounds was assessed., L’oxygène est essentiel à la cicatrisation des plaies et l’hypoxie est décrite comme une cause majeure de problèmes de cicatrisation. L’oxygénation tissulaire est un paramètre important dans la gestion clinique des plaies chroniques comme les ulcères diabétiques. Mais jusqu’à présent, aucune technique n’est capable de réaliser une mesure absolue, non-invasive et répétée de l’oxygénation directement dans un tissu. L’oxymétrie par Résonance Paramagnétique Electronique (RPE) est une technique qui permet de réaliser ce type de mesures mais n’a jamais été appliquée dans le contexte de cicatrisation de plaies diabétiques. Le but de la thèse était d’implémenter l’oxymétrie RPE pour suivre les variations en oxygénation dans les plaies diabétiques. La première partie de la thèse a consisté en la validation de la technique pour mesurer l’oxygénation dans les plaies. Ensuite, l’utilisation de l’oxymétrie RPE comme biomarqueur de réponse à un traitement dans les plaies diabétiques a été évaluée., (BIFA - Sciences biomédicales et pharmaceutiques) -- UCL, 2017
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- 2017
50. Influence des acides gras libres sur la fonction et la survie des cellules de la lignée ostéogénique et rôle de la lipotoxicité dans la pathogénie de l’ostéonécrose de la tête fémorale
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Rasschaert, Joanne, Gangji, Valérie, Lebrun, Philippe, Body, Jean-Jacques, Communi, Didier, Moreno Reyes, Mario Rodrigo, Jonas, Jean-Christophe JJC, Serteyn, Didier, Hardouin, Pierre, Gillet, Céline, Rasschaert, Joanne, Gangji, Valérie, Lebrun, Philippe, Body, Jean-Jacques, Communi, Didier, Moreno Reyes, Mario Rodrigo, Jonas, Jean-Christophe JJC, Serteyn, Didier, Hardouin, Pierre, and Gillet, Céline
- Abstract
L’os est un tissu dynamique, en remodelage constant grâce à un processus finement régulé impliquant des facteurs locaux et systémiques. Un déséquilibre entre la formation et la résorption osseuses, assurées respectivement par les ostéoblastes et les ostéoclastes, conduit à une altération de la microarchitecture de l’os, une augmentation du risque de fracture, et à l’apparition de pathologies telles que l’ostéonécrose et l’ostéoporose. Ces deux maladies ont pour caractéristiques communes une diminution du nombre de cellules stromales mésenchymateuses (MSC), les progéniteurs des ostéoblastes, et des anomalies fonctionnelles des MSC et des cellules ostéoblastiques (Ob). De surcroit, elles présentent toutes deux une accumulation d’adipocytes au sein de la moelle osseuse. De récentes publications suggèrent que cette accumulation d’adipocytes médullaires pourrait avoir des conséquences délétères sur la physiologie des cellules ostéoformatrices et de leurs progéniteurs, partageant ce même microenvironnement osseux. Une relation inverse entre l’excès d’adiposité médullaire et la masse osseuse est en effet aujourd’hui clairement établie. Par son importante activité sécrétrice de cytokines et d’adipokines ainsi que sa capacité à stocker et libérer des acides gras libres (AGL), l’adipocyte médullaire est capable de modifier la composition du microenvironnement osseux, et ainsi d’influencer le métabolisme et la fonction des cellules avoisinantes, et notamment des cellules osseuses. Afin d’étudier l’influence des AGL sur la survie et la fonction des cellules ostéogéniques, nous avons utilisé un AGL saturé, le palmitate (Palm ;C16 :0) et un AGL monoinsaturé, l’oléate (Ole ;C18 :1), tous deux étant particulièrement abondants dans l’organisme et l’alimentation de l’homme et couramment utilisés dans les études de lipotoxicité. Dans un premier temps, nous avons travaillé sur des MSC isolées de la moelle osseuse de sujets sains (HV-MSC), qui ont éventuellement été différenciées en Ob., Doctorat en Sciences biomédicales et pharmaceutiques (Médecine), info:eu-repo/semantics/nonPublished
- Published
- 2017
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