15 results on '"Horvat, Anemari"'
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2. Astrocytes with TDP-43 inclusions exhibit reduced noradrenergic cAMP and Ca2+ signaling and dysregulated cell metabolism
- Author
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Velebit, Jelena, Horvat, Anemari, Smolič, Tina, Prpar Mihevc, Sonja, Rogelj, Boris, Zorec, Robert, and Vardjan, Nina
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- 2020
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3. Astrocyte Specific Remodeling of Plasmalemmal Cholesterol Composition by Ketamine Indicates a New Mechanism of Antidepressant Action
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Lasič, Eva, Lisjak, Marjeta, Horvat, Anemari, Božić, Mićo, Šakanović, Aleksandra, Anderluh, Gregor, Verkhratsky, Alexei, Vardjan, Nina, Jorgačevski, Jernej, Stenovec, Matjaž, and Zorec, Robert
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- 2019
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4. Adrenergic activation attenuates astrocyte swelling induced by hypotonicity and neurotrauma
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Vardjan, Nina, Horvat, Anemari, Anderson, Jamie E., Yu, Dou, Croom, Deborah, Zeng, Xiang, Lužnik, Zala, Kreft, Marko, Teng, Yang D., Kirov, Sergei A., and Zorec, Robert
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- 2016
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5. The Activation of GPR27 Increases Cytosolic L-Lactate in 3T3 Embryonic Cells and Astrocytes.
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Dolanc, Dorian, Zorec, Tomaž M., Smole, Zala, Maver, Anja, Horvat, Anemari, Pillaiyar, Thanigaimalai, Trkov Bobnar, Saša, Vardjan, Nina, Kreft, Marko, Chowdhury, Helena Haque, and Zorec, Robert
- Subjects
MONOCARBOXYLATE transporters ,FLUORESCENCE resonance energy transfer ,ORPHANS ,ASTROCYTES - Abstract
G-protein-coupled receptors (GPCRs) represent a family with over 800 members in humans, and one-third of these are targets for approved drugs. A large number of GPCRs have unknown physiologic roles. Here, we investigated GPR27, an orphan GPCR belonging to the family of super conserved receptor expressed in the brain, with unknown functions. Cytosolic levels of L-lactate ([lactate]
i ), the end product of aerobic glycolysis, were measured with the Laconic fluorescence resonance energy transfer nanosensor. In single 3T3 wild-type (WT) embryonic cells, the application of 8535 (1 µM), a surrogate agonist known to activate GPR27, resulted in an increase in [lactate]i . Similarly, an increase was recorded in primary rat astrocytes, a type of neuroglial cell abundant in the brain, which contain glycogen and express enzymes of aerobic glycolysis. In CRISPR-Cas9 GPR27 knocked out 3T3 cells, the 8535-induced increase in [lactate]i was reduced compared with WT controls. Transfection of the GPR27-carrying plasmid into the 3T3KOGPR27 cells rescued the 8535-induced increase in [lactate]i . These results indicate that stimulation of GPR27 enhances aerobic glycolysis and L-lactate production in 3T3 cells and astrocytes. Interestingly, in the absence of GPR27 in 3T3 cells, resting [lactate]i was increased in comparison with controls, further supporting the view that GPR27 regulates L-lactate homeostasis. [ABSTRACT FROM AUTHOR]- Published
- 2022
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6. Astrocyte arborization enhances Ca2+ but not cAMP signaling plasticity.
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Pirnat, Samo, Božić, Mićo, Dolanc, Dorian, Horvat, Anemari, Tavčar, Petra, Vardjan, Nina, Verkhratsky, Alexei, Zorec, Robert, and Stenovec, Matjaž
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- 2021
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7. Lactate as an Astroglial Signal Augmenting Aerobic Glycolysis and Lipid Metabolism.
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Horvat, Anemari, Zorec, Robert, and Vardjan, Nina
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LIPID metabolism ,LACTATION ,G protein coupled receptors ,GLYCOLYSIS ,HOMEOSTASIS - Abstract
Astrocytes, heterogeneous neuroglial cells, contribute to metabolic homeostasis in the brain by providing energy substrates to neurons. In contrast to predominantly oxidative neurons, astrocytes are considered primarily as glycolytic cells. They take up glucose from the circulation and in the process of aerobic glycolysis (despite the normal oxygen levels) produce L-lactate, which is then released into the extracellular space via lactate transporters and possibly channels. Astroglial L-lactate can enter neurons, where it is used as a metabolic substrate, or exit the brain via the circulation. Recently, L-lactate has also been considered to be a signaling molecule in the brain, but the mechanisms of L-lactate signaling and how it contributes to the brain function remain to be fully elucidated. Here, we provide an overview of L-lactate signaling mechanisms in the brain and present novel insights into the mechanisms of L-lactate signaling via G-protein coupled receptors (GPCRs) with the focus on astrocytes. We discuss how increased extracellular L-lactate upregulates cAMP production in astrocytes, most likely via L-lactate-sensitive G
s -protein coupled GPCRs. This activates aerobic glycolysis, enhancing L-lactate production and accumulation of lipid droplets, suggesting that L-lactate augments its own production in astrocytes (i.e., metabolic excitability) to provide more L-lactate for neurons and that astrocytes in conditions of increased extracellular L-lactate switch to lipid metabolism. [ABSTRACT FROM AUTHOR]- Published
- 2021
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8. Astrocytes in stress accumulate lipid droplets.
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Smolič, Tina, Tavčar, Petra, Horvat, Anemari, Černe, Urška, Halužan Vasle, Ana, Tratnjek, Larisa, Kreft, Mateja Erdani, Scholz, Nicole, Matis, Maja, Petan, Toni, Zorec, Robert, and Vardjan, Nina
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- 2021
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9. Astroglial cAMP signalling in space and time.
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Horvat, Anemari and Vardjan, Nina
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Highlights • Genetically encoded fluorescent cAMP sensors have enabled the first measurements of the temporal dynamics of cAMP signalling in living astrocytes. • Compared with Ca2+ signalling with fast phasic dynamics, cAMP signalling in astrocytes -exhibits >4-fold slower tonic dynamics. • Ca2+ potentiates cAMP signalling -in astrocytes, indicating cross-talk between the Ca2+- and cAMP-signalling pathways. • Astroglial cAMP signalling in subcellular compartments needs to be evaluated in the future. Abstract To maintain a high level of specificity and normal cell function, the cyclic adenosine monophosphate (cAMP) pathway is tightly regulated in space and time. Recent advances in cAMP reporter technology have provided insights into spatio-temporal characteristics of cAMP signalling in individual living cells, including astrocytes. Astrocytes are glial cells in the central nervous system with many homeostatic functions. In contrast to neurons, astrocytes are electrically silent, but, in response to extracellular stimuli through activation of surface receptors, they can increase intracellular levels of secondary messengers, e.g. Ca2+ and cAMP. This enables them to communicate with neighbouring cells, such as neurons and endothelial cells of blood vessels. The dynamics of receptor-mediated Ca2+ signalling in astrocytes has been extensively studied in the past in contrast to cAMP signalling. Here, we present the first insights into the temporal dynamics of cAMP signalling in living astrocytes, which revealed that cAMP signals in astrocytes exhibit tonic dynamics and are slower than Ca2+ signals with phasic dynamics. We debate on the heterogeneity of basal cAMP levels in astrocytes and how hypotonicity-induced astrocyte swelling affects temporal dynamics of cAMP signalling. Understanding the spatio-temporal characteristics of cAMP signalling in astrocytes is of extreme importance because cAMP governs many important cellular processes and any malfunctions may lead to pathology. [ABSTRACT FROM AUTHOR]
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- 2019
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10. Enhancement of Astroglial Aerobic Glycolysis by Extracellular Lactate-Mediated Increase in cAMP.
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Vardjan, Nina, Chowdhury, Helena H., Horvat, Anemari, Velebit, Jelena, Malnar, Maja, Muhič, Marko, Kreft, Marko, Krivec, Špela G., Bobnar, Saša T., Miš, Katarina, Pirkmajer, Sergej, Offermanns, Stefan, Henriksen, Gjermund, Storm-Mathisen, Jon, Bergersen, Linda H., and Zorec, Robert
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GLYCOLYSIS ,ASTROCYTES ,LACTATES - Abstract
Besides being a neuronal fuel, L-lactate is also a signal in the brain. Whether extracellular L-lactate affects brain metabolism, in particular astrocytes, abundant neuroglial cells, which produce L-lactate in aerobic glycolysis, is unclear. Recent studies suggested that astrocytes express low levels of the L-lactate GPR81 receptor (EC
50 ≈ 5 mM) that is in fat cells part of an autocrine loop, in which the Gi-protein mediates reduction of cytosolic cyclic adenosine monophosphate (cAMP). To study whether a similar signaling loop is present in astrocytes, affecting aerobic glycolysis, we measured the cytosolic levels of cAMP, D-glucose and L-lactate in single astrocytes using fluorescence resonance energy transfer (FRET)-based nanosensors. In contrast to the situation in fat cells, stimulation by extracellular L-lactate and the selective GPR81 agonists, 3-chloro-5-hydroxybenzoic acid (3Cl-5OH-BA) or 4-methyl-N-(5-(2-(4-methylpiperazin- 1-yl)-2-oxoethyl)-4-(2-thienyl)-1,3-thiazol-2-yl)cyclohexanecarboxamide (Compound 2), like adrenergic stimulation, elevated intracellular cAMP and L-lactate in astrocytes, which was reduced by the inhibition of adenylate cyclase. Surprisingly, 3Cl-5OH-BA and Compound 2 increased cytosolic cAMP also in GPR81-knock out astrocytes, indicating that the effect is GPR81-independent and mediated by a novel, yet unidentified, excitatory L-lactate receptor-like mechanism in astrocytes that enhances aerobic glycolysis and L-lactate production via a positive feedback mechanism. [ABSTRACT FROM AUTHOR]- Published
- 2018
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11. Adrenergic stimulation of single rat astrocytes results in distinct temporal changes in intracellular Ca2+ and cAMP-dependent PKA responses.
- Author
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Horvat, Anemari, Zorec, Robert, and Vardjan, Nina
- Abstract
During the arousal and startle response, locus coeruleus neurons, innervating practically all brain regions, release catecholamine noradrenaline, which reaches neural brain cells, including astrocytes. These glial cells respond to noradrenergic stimulation by simultaneous activation of the α- and β-adrenergic receptors (ARs) in the plasma membrane with increasing cytosolic levels of Ca 2+ and cAMP, respectively. AR-activation controls a myriad of processes in astrocytes including glucose metabolism, gliosignal vesicle homeostasis, gene transcription, cell morphology and antigen-presenting functions, all of which have distinct temporal characteristics. It is known from biochemical studies that Ca 2+ and cAMP signals in astrocytes can interact, however it is presently unclear whether the temporal properties of the two second messengers are time associated upon AR-activation. We used confocal microscopy to study AR agonist-induced intracellular changes in Ca 2+ and cAMP in single cultured cortical rat astrocytes by real-time monitoring of the Ca 2+ indicator Fluo4-AM and the fluorescence resonance energy transfer-based nanosensor A-kinase activity reporter 2 (AKAR2), which reports the activity of cAMP via its downstream effector protein kinase A (PKA). The results revealed that the activation of α 1 -ARs by phenylephrine triggers periodic (phasic) Ca 2+ oscillations within 10 s, while the activation of β-ARs by isoprenaline leads to a ∼10-fold slower tonic rise to a plateau in cAMP/PKA activity devoid of oscillations. Thus the concomitant activation of α- and β-ARs triggers the Ca 2+ and cAMP second messenger systems in astrocytes with distinct temporal properties, which appears to be tailored to regulate downstream effectors in different time domains. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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12. Memory Formation Shaped by Astroglia.
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Zorec, Robert, Horvat, Anemari, Vardjan, Nina, and Verkhratsky, Alexei
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ASTROCYTES ,MEMORY ,CENTRAL nervous system physiology ,PHYSIOLOGY - Abstract
Astrocytes, the most heterogeneous glial cells in the central nervous system (CNS), execute a multitude of homeostatic functions and contribute to memory formation. Consolidation of synaptic and systemic memory is a prolonged process and hours are required to form long-term memory. In the past, neurons or their parts have been considered to be the exclusive cellular sites of these processes, however, it has now become evident that astrocytes provide an important and essential contribution to memory formation. Astrocytes participate in the morphological remodeling associated with synaptic plasticity, an energy-demanding process that requires mobilization of glycogen, which, in the CNS, is almost exclusively stored in astrocytes. Synaptic remodeling also involves bidirectional astroglial-neuronal communication supported by astroglial receptors and release of gliosignaling molecules. Astroglia exhibit cytoplasmic excitability that engages second messengers, such as Ca
2+ , for phasic, and cyclic adenosine monophosphate (cAMP), for tonic signal coordination with neuronal processes. The detection of signals by astrocytes and the release of gliosignaling molecules, in particular by vesicle-based mechanisms, occurs with a significant delay after stimulation, orders of magnitude longer than that present in stimulus-secretion coupling in neurons. These particular arrangements position astrocytes as integrators ideally tuned to support time-dependent memory formation. [ABSTRACT FROM AUTHOR]- Published
- 2015
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13. Cover Image, Volume 69, Issue 12.
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Pirnat, Samo, Božić, Mićo, Dolanc, Dorian, Horvat, Anemari, Tavčar, Petra, Vardjan, Nina, Verkhratsky, Alexei, Zorec, Robert, and Stenovec, Matjaž
- Published
- 2021
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14. Ca2+ as the prime trigger of aerobic glycolysis in astrocytes.
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Horvat, Anemari, Muhič, Marko, Smolič, Tina, Begić, Ena, Zorec, Robert, Kreft, Marko, and Vardjan, Nina
- Abstract
[Display omitted] • Ca
2+ signals are key triggers of augmented aerobic glycolysis in astrocytes. • cAMP aids to Ca2+ -driven increase in aerobic glycolysis in astrocytes. • Aerobic glycolysis in astrocytes depends on extracellular d -glucose. • Aerobic glycolysis in astrocytes depends on glycogen shunt activity. Astroglial aerobic glycolysis, a process during which d -glucose is converted to l -lactate, a brain fuel and signal, is regulated by the plasmalemmal receptors, including adrenergic receptors (ARs) and purinergic receptors (PRs), modulating intracellular Ca2+ and cAMP signals. However, the extent to which the two signals regulate astroglial aerobic glycolysis is poorly understood. By using agonists to stimulate intracellular α 1 -/β-AR-mediated Ca2+ /cAMP signals, β-AR-mediated cAMP and P 2 R-mediated Ca2+ signals and genetically encoded fluorescence resonance energy transfer-based glucose and lactate nanosensors in combination with real-time microscopy, we show that intracellular Ca2+ , but not cAMP, initiates a robust increase in the concentration of intracellular free d -glucose ([glc] i) and l -lactate ([lac] i), both depending on extracellular d -glucose, suggesting Ca2+ -triggered glucose uptake and aerobic glycolysis in astrocytes. When the glycogen shunt, a process of glycogen remodelling, was inhibited, the α 1 -/β-AR-mediated increases in [glc] i and [lac] i were reduced by ∼65 % and ∼30 %, respectively, indicating that at least ∼30 % of the utilization of d -glucose is linked to glycogen remodelling and aerobic glycolysis. Additional activation of β-AR/cAMP signals aided to α 1 -/β-AR-triggered [lac] i increase, whereas the [glc] i increase was unaltered. Taken together, an increase in intracellular Ca2+ is the prime mechanism of augmented aerobic glycolysis in astrocytes, while cAMP has only a moderate role. The results provide novel information on the signals regulating brain metabolism and open new avenues to explore whether astroglial Ca2+ signals are dysregulated and contribute to neuropathologies with impaired brain metabolism. [ABSTRACT FROM AUTHOR]- Published
- 2021
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15. ERNEST COST action overview on the (patho)physiology of GPCRs and orphan GPCRs in the nervous system.
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Birgül Iyison, Necla, Abboud, Clauda, Abboud, Dayana, Abdulrahman, Abdulrasheed O., Bondar, Ana‐Nicoleta, Dam, Julie, Georgoussi, Zafiroula, Giraldo, Jesús, Horvat, Anemari, Karoussiotis, Christos, Paz‐Castro, Alba, Scarpa, Miriam, Schihada, Hannes, Scholz, Nicole, Güvenc Tuna, Bilge, and Vardjan, Nina
- Abstract
G protein‐coupled receptors (GPCRs) are a large family of cell surface receptors that play a critical role in nervous system function by transmitting signals between cells and their environment. They are involved in many, if not all, nervous system processes, and their dysfunction has been linked to various neurological disorders representing important drug targets. This overview emphasises the GPCRs of the nervous system, which are the research focus of the members of ERNEST COST action (CA18133) working group ‘Biological roles of signal transduction’. First, the (patho)physiological role of the nervous system GPCRs in the modulation of synapse function is discussed. We then debate the (patho)physiology and pharmacology of opioid, acetylcholine, chemokine, melatonin and adhesion GPCRs in the nervous system. Finally, we address the orphan GPCRs, their implication in the nervous system function and disease, and the challenges that need to be addressed to deorphanize them. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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