The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Electrophysiology of Islet Cells
Abstract
Stimulus-Secretion Coupling (SSC) of pancreatic islet cells comprises electrical activity. Changes of the membrane potential (V(m)) are regulated by metabolism-dependent alterations in ion channel activity. This coupling is best explored in beta-cells. The effect of glucose is directly linked to mitochondrial metabolism as the ATP/ADP ratio determines the open probability of ATP-sensitive K(+) channels (K(ATP) channels). Nucleotide sensitivity and concentration in the direct vicinity of the channels are controlled by several factors including phospholipids, fatty acids, and kinases, e.g., creatine and adenylate kinase. Closure of K(ATP) channels leads to depolarization of beta-cells via a yet unknown depolarizing current. Ca(2+) influx during action potentials (APs) results in an increase of the cytosolic Ca(2+) concentration ([Ca(2+)](c)) that triggers exocytosis. APs are elicited by the opening of voltage-dependent Na(+) and/or Ca(2+) channels and repolarized by voltage- and/or Ca(2+)-dependent K(+) channels. At a constant stimulatory glucose concentration APs are clustered in bursts that are interrupted by hyperpolarized interburst phases. Bursting electrical activity induces parallel fluctuations in [Ca(2+)](c) and insulin secretion. Bursts are terminated by I(Kslow) consisting of currents through Ca(2+)-dependent K(+) channels and K(ATP) channels. This review focuses on structure, characteristics, physiological function, and regulation of ion channels in beta-cells. Info…
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“At 10 mM glucose, the active and silent phases last 5-10 s and 10-20 s, respectively and there are 2-4 bursts/min (154, 273, 570).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [154]
In the citing paper
“A number of hormones and neurotransmitters (e.g. somatostatin and adrenaline) transiently repolarise the β-cell and inhibit action potential firing and insulin secretion (154, 543).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [154]
In the citing paper
“Increasing glucose concentrations produce a progressive increase in burst duration at the expense of the repolarized intervals until firing finally becomes continuous, usually above ~20 mM glucose (154, 273).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [154]
Citations
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“Electrophysiological Characteristics The first measurements of single beta cell KATP channel currents were performed in 1984 by Cook and Hales (Cook and Hales 1984) in inside/outside patches where they could show the inhibition by cytosolic ATP.”
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“The existence of BK channels in pancreatic beta cells and insulin-secreting cell lines has been verified by several groups (Braun et al. 2008; MacDonald et al. 2002a; Ribalet et al. 1988; Satin et al. 1989; Kukuljan et al. 1991; D€ufer et al. 2011).”
BackgroundInfluentialTransient receptor potential M3 channels are ionotropic steroid receptors in pancreatic β cells
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Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men
Rorsman, P., & Ashcroft, F. M. (2018) · Physiological Reviews · doi:10.1152/physrev.00008.2017 · Cited by 793
Metabolic Signaling in Fuel-Induced Insulin Secretion
Prentki, M., Matschinsky, F. M., & Madiraju, S. R. M. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.05.018 · Cited by 548
“2 and the activating effect of MgADP on the SUR1 component of the channel (Drews et al., 2010; Proks et al., 2010).”
BackgroundOxidative stress and beta-cell dysfunction
Drews, G., Krippeit-Drews, P., & Düfer, M. (2010) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-010-0862-9 · Cited by 315
“KATP channels are closed by ATP deriving from oxidative phosphorylation of (specialised) mitochondrial respiratory chains (for review see [97]).”
BackgroundSelf-citationCalcium signaling in pancreatic β-cells in health and in Type 2 diabetes
Gilon, P., Chae, H., Rutter, G. A., & Ravier, M. A. (2014) · Cell Calcium · doi:10.1016/j.ceca.2014.09.001 · Cited by 221
“001 he scope of this article to review all of these mechanisms, but elevant informations can be found elsewhere [19,22,58,63].”
BackgroundSerotonin regulates glucose-stimulated insulin secretion from pancreatic β cells during pregnancy
Ohara‐Imaizumi, M., Kim, H., Yoshida, M., Fujiwara, T., Aoyagi, K., Toyofuku, Y., Nakamichi, Y., Nishiwaki, C., Okamura, T., Uchida, T., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310953110 · Cited by 176
“Glucose also depolarizes β cells: Rising ATP from glucose catabolism depolarizes the cell by closing ATP-sensitive K channels, which causes Ca to enter the cell through voltagegated Ca channels and trigger insulin granule exocytosis (24).”
BackgroundGuo, J. H., Chen, H., Ruan, Y. C., Zhang, X. L., Zhang, X. H., Fok, K. L., Tsang, L. L., Yu, M. K., Huang, W. Q., Sun, X., et al. (2014) · Nature Communications · doi:10.1038/ncomms5420 · Cited by 157
Functional Role of Serotonin in Insulin Secretion in a Diet-Induced Insulin-Resistant State
Kim, K., Oh, C., Ohara‐Imaizumi, M., Park, S., Namkung, J., Yadav, V. K., Tamarina, N. A., Roe, M. W., Philipson, L. H., Karsenty, G., et al. (2014) · Endocrinology · doi:10.1210/en.2014-1687 · Cited by 135
Cao, D.-S., Zhong, L., Hsieh, T.-H. J., Abooj, M., Bishnoi, M., Hughes, L. K., & Premkumar, L. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038005 · Cited by 136
“The most predominant mechanism of insulin secretion in response to increased blood glucose levels is by the triggering pathway brought about by alteration in ATP/ADP ratio that results in the block of KATP channel, membrane depolarization, Ca 2+ influx through voltage-gated Ca channels, and exocytosis of insulin conta…”
BackgroundKono, T., Ahn, G., Moss, D. R., Gann, L., Zarain‐Herzberg, Á., Nishiki, Y., Fueger, P. T., Ogihara, T., & Evans‐Molina, C. (2012) · Molecular Endocrinology · doi:10.1210/me.2011-1181 · Cited by 116
Bardy, G., Virsolvy, A., Quignard, J., Ravier, M., Bertrand, G., Dalle, S., Cros, G., Magous, R., Richard, S., & Oiry, C. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12194 · Cited by 110
“…50–90% of the global voltagedependent Ca2+ current in mouse beta cells (Plant, 1988; Gilon et al., 1997) and are responsible for the long-lasting elevation of [Ca2+]i required for insulin secretion and beta cell function (Satin et al., 1995; Horvath et al., 1998; Mears, 2004; Drews et al., 2010).”
BackgroundRamadan, J. W., Steiner, S. R., O’Neill, C. M., & Nunemaker, C. S. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.08.005 · Cited by 104
Functional and physiopathological implications of TRP channels.
Smani, T., Shapovalov, G., Skryma, R., Prevarskaya, N., & Rosado, J. (2015) · Biochimica et Biophysica Acta · doi:10.1016/j.bbamcr.2015.04.016 · Cited by 98
“The nature of this background current, which might be due to Cl efflux or cation influx, remains unknown [62], but TRP channels have been presented as candidates for this depolarizing current [63,64].”
BackgroundThe Pancreatic β-Cell: A Bioenergetic Perspective
Nicholls, D. G. (2016) · Physiological Reviews · doi:10.1152/physrev.00009.2016 · Cited by 100
Glucose-Stimulated Insulin Secretion Fundamentally Requires H2O2 Signaling by NADPH Oxidase 4
Plecitá‐Hlavatá, L., Jabůrek, M., Holendová, B., Tauber, J. A., Pavluch, V., Berková, Z., Cahová, M., Schröder, K., Brandes, R. P., Siemen, D., et al. (2020) · Diabetes · doi:10.2337/db19-1130 · Cited by 96
“The resulting Ca(21) entry stimulates Ca(21)-dependent exocytosis of the insulin-containing secretory granules (8).”
BackgroundIonic mechanisms in pancreatic β cell signaling
Yang, S. N., Shi, Y., Yang, G., Li, Y., Yu, J. H., & Berggren, P. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1680-6 · Cited by 92
“To timely and accurately release insulin in response to changes in blood glucose levels, a series of ionic events, namely fluxes of K, Na, Ca and Cl across the b cell membranes occur [1, 2].”
BackgroundInfluentialBest, J. M., & Kamp, T. (2011) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2011.08.014 · Cited by 86
“Membrane microdomains and excitation-secretion coupling LTCCs provide a critical influx of Ca2+ necessary for secretion of hormones in some cell types [100,101].”
BackgroundZuccotti, A., Clementi, S., Reinbothe, T., Torrente, A., Vandael, D., & Pirone, A. (2011) · TIPS - Trends in Pharmacological Sciences · doi:10.1016/j.tips.2011.02.012 · Cited by 86
KCNQ1 Long QT Syndrome Patients Have Hyperinsulinemia and Symptomatic Hypoglycemia
Torekov, S. S., Iepsen, E., Christiansen, M., Linneberg, A., Pedersen, O., Holst, J. J., Kanters, J. K., & Hansen, T. (2014) · Diabetes · doi:10.2337/db13-1454 · Cited by 84
“However, as activation of Kv channels requires membrane depolarization, targeting Kv channels affect insulin secretion only in the presence of elevated glucose concentrations or other depolarizing stimuli (39,40).”
BackgroundReinbothe, T. M., Alkayyali, S., Ahlqvist, E., Tuomi, T., Isomaa, B., Lyssenko, V., & Renström, E. (2013) · Diabetologia · doi:10.1007/s00125-012-2758-z · Cited by 84
“3) is most important appears to be species dependent and to differ between rodents and humans [3].”
BackgroundContribution of Oxidative Stress and Impaired Biogenesis of Pancreatic β-Cells to Type 2 Diabetes
Ježek, P., Jabůrek, M., & Plecitá‐Hlavatá, L. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2018.7656 · Cited by 89
“The resulting elevated ATP/ADP ratio closes the plasma membrane ATP-sensitive K channel (KATP), which then initiates orchestra of other channel events substantiating plasma membrane depolarization (72).”
BackgroundFatty Acid-Stimulated Insulin Secretion vs. Lipotoxicity
Ježek, P., Jabůrek, M., Holendová, B., & Plecitá‐Hlavatá, L. (2018) · Molecules · doi:10.3390/molecules23061483 · Cited by 87
“The increasing ATP/ADP ratio affects the plasma membrane ATP-sensitive K+ channel (KATP), which closes and initiates concerted events of several other channels, leading to plasma membrane depolarization [12].”
BackgroundCeramide formation as a target in beta-cell survival and function
Lang, F., Ullrich, S., & Gulbins, E. (2011) · Expert opinion on therapeutic targets · doi:10.1517/14728222.2011.588209 · Cited by 78
“The Ca signal is terminated by the opening of a variety of voltage- and calcium-regulated K channels [153-155].”
Ion channels and regulation of insulin secretion in human β-cells: a computational systems analysis
Fridlyand, L. E., Jacobson, D. A., & Philipson, L. H. (2013) · Islets · doi:10.4161/isl.24166 · Cited by 78
“The whole-cell Ca current in mammalian β-cells flows principally through the voltage-gated Ca channels.(1,3,37) Whole-cell Na channel gating kinetics have incomplete inactivation of macroscopic currents for repolarization to subthreshold voltages.”
BackgroundResultInfluentialUchida, K., & Tominaga, M. (2011) · Endocrine Journal · doi:10.1507/endocrj.ej11-0130 · Cited by 77
“for the increase in [Ca]i is Ca2+ influx through L-type VGCCs, but recent electrophysiological studies indicated that many ion channels can contribute to Ca2+ signaling and changes in membrane potentials, and their relative importance has been examined [4, 5].”
BackgroundPurinergic signalling in endocrine organs
Burnstock, G. (2013) · Purinergic Signalling · doi:10.1007/s11302-013-9396-x · Cited by 68
“Sympathetic nerve stimulation inhibited insulin secretion, probably via α2A receptor mediated opening of ATPdependent K channels [132,324].”
BackgroundLi, X., Herrington, J., Petrov, A., Ge, L., Eiermann, G., Xiong, Y., Jensen, M., Hohmeier, H., Newgard, C., Garcia, M., et al. (2013) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.112.199083 · Cited by 72
“Hormone release is tightly controlled by ion channels that regulate cell membrane potential and calcium influx (Rorsman, 1997; Kanno et al., 2002; Drews et al., 2010).”
BackgroundVierra, N. C., Dadi, P. K., Jeong, I., Dickerson, M., Powell, D. R., & Jacobson, D. A. (2015) · Diabetes · doi:10.2337/db15-0280 · Cited by 71
“The closure of KATP channels results in Vm depolarization to a plateau potential from which action potentials (APs) fire, allowing Ca influx through VDCCs, resulting in insulin secretion (1,2).”
BackgroundPurinergic signalling in the pancreas in health and disease
Burnstock, G., & Novak, I. (2012) · Journal of Endocrinology · doi:10.1530/joe-11-0434 · Cited by 79
Immunocytochemical markers of neuronal maturation in human diagnostic neuropathology
Sarnat, H. B. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1988-4 · Cited by 77
Islam, M. S. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-0265-3_42 · Cited by 79
“A handful of ion channels are known to be involved in mediating these two interdependent events [3].”
BackgroundThe Edges of Pancreatic Islet β Cells Constitute Adhesive and Signaling Microdomains.
Geron, E., Boura-Halfon, S., Schejter, E., & Shilo, B. (2015) · Cell Reports · doi:10.1016/j.celrep.2014.12.031 · Cited by 62
“In mouse b cells, the action potentials are evokedmainly by Ca2+ influx from the extracellular space through CaV (Drews et al., 2010).”
InfluentialAquaporins in salivary glands and pancreas.
Delporte, C. (2014) · Biochimica et Biophysica Acta · doi:10.1016/j.bbagen.2013.08.007 · Cited by 62
“Indeed, ß-cells exposed to hypotonic stress encounter cell swelling which activates volume-regulated anion channel and cell depolarization, leading to activation of voltage-sensitive Ca channels, calcium entry and thereby insulin secretion [156,157] (Fig.”
BackgroundA review on insulin trafficking and exocytosis
Vakilian, M., Tahamtani, Y., & Ghaedi, K. (2019) · Gene · doi:10.1016/j.gene.2019.04.063 · Cited by 81
Transient Receptor Potential Cation Channels in Pancreatic β Cells
Colsoul, B., Vennekens, R., & Nilius, B. (2011) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2011_2 · Cited by 67
Aquaglyceroporins: Drug Targets for Metabolic Diseases?
Calamita, G., Perret, J., & Delporte, C. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00851 · Cited by 57
“extracellular hypotonicity, β-cells swelling induces the activation of volume-regulated anion channels (VRAC), leading to subsequent cell depolarization, activation of voltage-dependent calcium channel, increase in intracellular calcium concentration, and finally insulin release (Best et al., 1996; Drews et al., 2010).”
BackgroundFeng, A. L., Xiang, Y., Gui, L., Kaltsidis, G., Feng, Q., & Lu, W.-Y. (2017) · Diabetologia · doi:10.1007/s00125-017-4239-x · Cited by 70
Mathematical models of electrical activity of the pancreatic β-cell: A physiological review
Félix‐Martínez, G. J., & Godínez-Fernández, J. R. (2014) · Islets · doi:10.4161/19382014.2014.949195 · Cited by 67
“The detailed electrophysiological properties of ionic channels in b-cells can be found elsewhere.(17,18,20) The expression of specific ionic channels differs between species,(22,23) which is reflected in the corresponding pattern of electrical activity (for recent reviews see refs.”
BackgroundMugabo, Y., Zhao, S., Lamontagne, J., Al‐Mass, A., Peyot, M., Corkey, B. E., Joly, E. C., Madiraju, S. R. M., & Prentki, M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.763060 · Cited by 54
“2 and the activating effect of MgADP on the SUR1 component of the channel (83, 84).”
BackgroundGlucose and lipid metabolism abnormalities in C ushing's syndrome
Salehidoost, R., & Korbonits, M. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13143 · Cited by 57
“The elevation of Ca in beta cells accelerates insulin exocytosis.(80) SGK1, a regulator of K channels, is under strong transcriptional control of GCs.”
BackgroundSchultheis, J., Beckmann, D., Mulac, D., Müller, L., Esselen, M., & Düfer, M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7518510 · Cited by 50
“, acute, stimulatory effects at low concentrations and a negative impact at higher concentrations, is also postulated for nitric oxide [30].”
BackgroundSelf-citationSignaling complexes of voltage-gated calcium channels
Turner, R. W., Anderson, D., & Zamponi, G. W. (2011) · Channels · doi:10.4161/chan.5.5.16473 · Cited by 46
“contraction coupling in the heart and muscle, insulin secretion and calcium dependent gene transcription.(17-21) Along these lines, different calcium channels isoforms are targeted by clinically active drugs such as analgesics, general anesthetics, antiepileptics and cardioactive drugs,(12,15,22-24) and mutations in v…”
BackgroundRevisiting the metabolic syndrome: the emerging role of aquaglyceroporins
da Silva, I. V., Rodrigues, J. S., Rebelo, I., Miranda, J. P., & Soveral, G. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2781-4 · Cited by 47
The Pancreatic β-Cell: The Perfect Redox System
Ježek, P., Holendová, B., Jabůrek, M., Tauber, J. A., Dlasková, A., & Plecitá‐Hlavatá, L. (2021) · Antioxidants · doi:10.3390/antiox10020197 · Cited by 38
“At about 7 mM glucose, the KATP channel current is so low that together with “synergic” channels, the attained depolarization leads to the action potential firing [91,92].”
BackgroundInfluentialModulation of Ionic Channels and Insulin Secretion by Drugs and Hormones in Pancreatic Beta Cells
Velasco, M., Díaz‐García, C. M., Larqué, C., & Hiriart, M. (2016) · Molecular Pharmacology · doi:10.1124/mol.116.103861 · Cited by 41
“The ATP hydrolysis occurs in NBD1, which is a high-affinity site for ATP or MgATP, whereas NBD2 has low-affinity to MgATP orMgADP and intrinsic ATPase activity (Drews et al., 2010; Yang et al., 2014a).”
BackgroundAquaporins Involvement in Pancreas Physiology and in Pancreatic Diseases
Arsenijevic, T., Perret, J., Laethem, J. V., & Delporte, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20205052 · Cited by 37
“An increase in β-cell volume is known to activate the volume-regulated anion channel (VRAC) and induce plasma membrane depolarization, which in turn stimulates voltage-sensitive calcium channels and leads to intracellular calcium concentration increase and insulin release [70,71].”
BackgroundKidd, M., Modlin, I., Bodei, L., & Drozdov, I. (2015) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2014.12.008 · Cited by 36
Regulation of glucose‐stimulated insulin secretion by ATPase Inhibitory Factor 1 (IF1)
Kahancová, A., Sklenář, F., Ježek, P., & Dlasková, A. (2018) · FEBS Letters · doi:10.1002/1873-3468.12991 · Cited by 35
Update on the Protective Molecular Pathways Improving Pancreatic Beta-Cell Dysfunction
Puddu, A., Sanguineti, R., Mach, F., Dallegri, F., Viviani, G. L., & Montecucco, F. (2013) · Mediators of Inflammation · doi:10.1155/2013/750540 · Cited by 33
“gated Ca channels and insulin granule exocytosis [99, 100].”
Islam, M. S. (2020) · Cells · doi:10.3390/cells9030685 · Cited by 36
“The electrical activities and the [Ca2+]i oscillations are generated by concerted participation of a unique repertoire of ion channels present in the β-cells [4].”
BackgroundMathematical models of pancreatic islet size distributions
Jo, J., Hara, M., Ahlgren, U., Sorenson, R. L., & Periwal, V. (2012) · Islets · doi:10.4161/isl.18660 · Cited by 32
Kong, X.-C., Tu, Y.-F., Li, B.-F., Zhang, L.-M., Feng, L., Wang, L.-X., Zhang, L., Zhou, H.-R., Hua, X., & Ma, X.-S. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2019.08.009 · Cited by 32
“The transient receptor potential (TRP) channels have been hypothesized to be responsible for this inward cation current [9,10].”
BackgroundLupanine Improves Glucose Homeostasis by Influencing KATP Channels and Insulin Gene Expression
Wiedemann, M., Gurrola-Díaz, C., Vargas-Guerrero, B., Wink, M., García-López, P., & Düfer, M. (2015) · Molecules · doi:10.3390/molecules201019085 · Cited by 32
“, by mechanisms elevating intracellular cAMP concentration [12].”
BackgroundSelf-citationLiu, L., Wang, F., Lu, H.-Y., Ren, X.-M., & Zou, J.-H. (2014) · Islets · doi:10.4161/19382014.2014.962386 · Cited by 31
Transient Receptor Potential (TRP) Cation Channels in Diabetes
Colsoul, B., Nilius, B., & Vennekens, R. (2013) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026611313030004 · Cited by 24
Involvement of aquaglyceroporins in energy metabolism in health and disease.
Calamita, G., & Delporte, C. (2021) · Biochimie · doi:10.1016/j.biochi.2021.03.001 · Cited by 30
Mourad, N., Nenquin, M., & Henquin, J. (2012) · Endocrinology · doi:10.1210/en.2012-1450 · Cited by 30
Kv1.3: a potential pharmacological target for diabetes
Choi, B. H., & Hahn, S. J. (2010) · Acta Pharmacologica Sinica · doi:10.1038/aps.2010.133 · Cited by 28
High-resolution analysis of the cytosolic Ca2+ events in β cell collectives in situ
Postić, S., Sarikas, S., Pfabe, J., Pohorec, V., Bombek, L. K., Sluga, N., Klemen, M. S., Dolenšek, J., Korošak, D., Stožer, A., et al. (2021) · bioRxiv · doi:10.1101/2021.04.14.439796 · Cited by 29
Sakuma, K., Yabuki, C., Maruyama, M., Abiru, A., Komatsu, H., Negoro, N., Tsujihata, Y., Takeuchi, K., Habata, Y., & Mori, M. (2016) · Pharmacology Research & Perspectives · doi:10.1002/prp2.237 · Cited by 29
“Membrane depolarization of b-cells is necessary for the insulinotropic effect of fasiglifam Membrane depolarization is a fundamental event in the integration of excitatory signals during glucose-induced insulin secretion (MacDonald and Rorsman 2006; Drews et al. 2010).”
BackgroundArous, C., Ferreira, P. G., Dermitzakis, E. T., & Halban, P. A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.611111 · Cited by 35
“This rise in cytosolic Ca(2) stems from glucose metabolism, closure of ATPsensitive potassium channels, depolarization, opening of voltage-gated calcium channels, and calcium influx (41).”
BackgroundPfeiffer, T., Kraushaar, U., Düfer, M., Schönecker, S., Haspel, D., Günther, E., Drews, G., & Krippeit-Drews, P. (2011) · Pflügers Archiv: European Journal of Physiology · doi:10.1007/s00424-011-1029-z · Cited by 27
“Pancreatic beta-cells are unique as they exhibit oscillatory electrical activity known as slow waves in response to glucose [7].”
BackgroundMethodInfluentialSelf-citationChang, H.-Y., Chen, S.-L., Shen, M., Kung, M., Chuang, L., & Chen, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-03747-0 · Cited by 29
Teyani, R. L., & Moniri, N. H. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16225 · Cited by 24
“…glucose stimulus used to drive GSIS in these studies is variable in the non-basal state and ranges from 12 to 25 mM, which could produce differential levels of glycolysis and subsequent ATP:ADP ratios that drive depolarization-dependent insulin secretion (Drews et al., 2010; Morsi et al., 2020).”
BackgroundMetabolic amplification of insulin secretion by glucose is independent of β-cell microtubules.
Mourad, N., Nenquin, M., & Henquin, J. (2011) · American Journal of Physiology - Cell Physiology · doi:10.1152/ajpcell.00329.2010 · Cited by 24
Henquin, J., Mourad, N., & Nenquin, M. (2012) · FEBS Letters · doi:10.1016/j.febslet.2011.11.030 · Cited by 23
Alshahrani, S., & Difulvio, M. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0244 · Cited by 22
“This depolarisation gates voltage-dependent Ca2C channels promoting Ca2C influx, the trigger for exocytosis of insulin stored in granules (Drews et al. 2010).”
BackgroundMears, D., Zimliki, C., Atwater, I., Rojas, E., Glassman, M., Leighton, X., Pollard, H., & Srivastava, M. (2012) · Cellular Physiology and Biochemistry · doi:10.1159/000186926 · Cited by 22
Role of TRP Channels in Metabolism-Related Diseases
Wu, F., Bu, S., & Wang, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020692 · Cited by 23
“When the plasma membrane depolarizes to − 50 mV, the voltage-gated calcium channel opens, causing Ca 2+ inflow and an increase in cytoplasmic calcium ion concentration, and the increase in intracellular Ca 2+ concentration triggers the exocytosis of insulin-containing vesicles in β cells [85,86].”
BackgroundEsculentin-2CHa(1-30) and its analogues: stability and mechanisms of insulinotropic action.
Vasu, S., McGahon, M., Moffett, R., Curtis, T., Conlon, J., Abdel-Wahab, Y., & Flatt, P. (2017) · Journal of Endocrinology · doi:10.1530/joe-16-0453 · Cited by 21
“…detect the changes in blood glucose levels, and subsequent metabolism leads to increase in ATP levels that induces closure of plasma membrane K ATP channels and depolarisation resulting in the opening of voltage-gated Ca 2+ channels (VDCC) (McClenaghan 2007, Drews et al. 2010, Fu et al. 2013).”
BackgroundGarcía-Delgado, N., Velasco, M., Sánchez-Soto, C., Díaz-García, C. M., & Hiriart, M. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00040 · Cited by 19
Jensen, M. V., Haldeman, J. M., Zhang, H., Lu, D., Huising, M. O., Vale, W., Hohmeier, H. E., Rosenberg, P. B., & Newgard, C. B. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.491654 · Cited by 25
Calcium channels as therapeutic targets
Belardetti, F., & Zamponi, G. W. (2012) · Wiley Interdisciplinary Reviews Membrane Transport and Signalling · doi:10.1002/wmts.38 · Cited by 27
Henquin, J. (2017) · Biochimie · doi:10.1016/j.biochi.2017.07.002 · Cited by 22
“In both mouse and human β-cells, it is generated by closure of KATP channels in 89 the plasma membrane, which permits depolarization to the threshold potential at which voltage90 gated calcium channels open and allow Ca 2+ influx into the cell [9-14].”
BackgroundAtrial Natriuretic Peptide Affects Stimulus-Secretion Coupling of Pancreatic β-Cells
Undank, S., Kaiser, J. K., Sikimić, J., Düfer, M., Krippeit-Drews, P., & Drews, G. (2017) · Diabetes · doi:10.2337/db17-0392 · Cited by 18
“RPMI1640 medium was from PromoCell (Heidelberg, Germany), penicillin/streptomycin from Gibco BRL (Karlsruhe, Germany), atrial natriuretic factor (1-28) (mouse, rabbit, rat) trifluoroacetate salt from Bachem (Weil am Rhein, Germany), Rp-8-Br-PET-cGMPS from Biolog (Bremen, Germany), and PKI 14-22 amide, myristoylated (m…”
BackgroundMethodSelf-citationPohorec, V., Bombek, L. K., Klemen, M. S., Dolenšek, J., & Stožer, A. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.867663 · Cited by 17
Ca-induced Ca Release from Internal Stores in INS-1 Rat Insulinoma Cells.
Choi, K., Dong, S.-C., Kim, J., Kim, B., Lee, K. M., Kim, S.-H., Kim, D. K., Kim, S. H., & Park, H. (2011) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2011.15.1.53 · Cited by 16
“The depolarization of plasma membranes for activation of voltage-gated Ca channels (CaV) is one of the most critical events leading to a rise in [Ca]i and insulin secretion in β-cell [1-3,27,28].”
BackgroundWilhelmi, I., Grunwald, S., Gimber, N., Popp, O., Dittmar, G., Arumughan, A., Wanker, E. E., Laeger, T., Schmoranzer, J., Daumke, O., et al. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101151 · Cited by 15
“ATP-sensitive potassium channels in the plasma membrane are closed due to a rising ATP:ADP ratio, leading to membrane depolarization, followed by opening of voltage-dependent Ca 2 þ channels [5 e 7].”
Possible New Strategies for the Treatment of Congenital Hyperinsulinism
Sikimic, J., Hoffmeister, T., Gresch, A., Kaiser, J., Barthlen, W., Wolke, C., Wieland, I., Lendeckel, U., Krippeit‐Drews, P., Düfer, M., et al. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.545638 · Cited by 16
“This points to alterations in mitochondrial metabolism, which can cause changes in KATP channel activity independent of any direct interaction with the channel proteins (72).”
BackgroundSelf-citationExpression and function of ATP-dependent potassium channels in zebrafish islet β-cells
Emfinger, C. H., Welscher, A., Yan, Z., Wang, Y., Conway, H., Moss, J. B., Moss, L. G., Remedi, M. S., & Nichols, C. G. (2017) · Royal Society Open Science · doi:10.1098/rsos.160808 · Cited by 15
“In the pancreatic β-cell, ATP-sensitive potassium (KATP) channels link glucose metabolism and insulin secretion and are essential to the normal regulation of plasma glucose and other nutrients [1,2].”
BackgroundChanneling dysglycemia: ion-channel variations perturbing glucose homeostasis
Denton, J. S., & Jacobson, D. A. (2011) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2011.09.004 · Cited by 15
“Depolarization of the islet membrane activates many ion channels including VDCCs, voltage-gated sodium (NaV) channels, and potassium channels, whereas, hyperpolarization inactivates these channels [1, 3, 8, 23].”
BackgroundPancreatic beta-cells: Role of glycerol and aquaglyceroporin 7.
Virreira, M., Perret, J., & Delporte, C. (2011) · International Journal of Biochemistry and Cell Biology · doi:10.1016/j.biocel.2010.10.018 · Cited by 14
“…to hypotonic extracellular solutions induce cell swelling, activating volume-regulated anion channel (VRAC) and cell membrane depolarization, leading to activation of voltage-sensitive calcium channels, allowing calcium entry, and thereby insulin exocytosis (Best et al., 1996; Drews et al., 2010).”
BackgroundRegulatory effects of protein S-acylation on insulin secretion and insulin action
Chamberlain, L. H., Shipston, M. J., & Gould, G. W. (2021) · Open Biology · doi:10.1098/rsob.210017 · Cited by 13
Cieślak, M., & Roszek, K. (2014) · Acta Biochimica Polonica · doi:10.18388/abp.2014_1827 · Cited by 13
“On the contrary, stimulation of the sympathetic nerve endings inhibits insulin secretion by affecting the α2A adrenoceptor acting through the ATP-dependent K+-channel (Drews et al., 2010; Burnstock, 2013).”
BackgroundA computational systems analysis of factors regulating α cell glucagon secretion
Fridlyand, L. E., & Philipson, L. H. (2012) · Islets · doi:10.4161/isl.22193 · Cited by 12
Evidence against a Ca2+-induced potentiation of dehydrogenase activity in pancreatic beta-cells
Drews, G., Bauer, C., Edalat, A., Düfer, M., & Krippeit-Drews, P. (2015) · Pflügers Archiv: European Journal of Physiology · doi:10.1007/s00424-015-1707-3 · Cited by 12
Self-citationLanglhofer, G., Kögel, A., & Schaefer, M. (2021) · Cell Calcium · doi:10.1016/j.ceca.2021.102469 · Cited by 11
Leech, C. A., Kopp, R., Nelson, H. A., Nandi, J., & Roe, M. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.767681 · Cited by 11
“2 L-type Ca(2) channels (28 –30) that is important for triggering insulin secretion (31, 32).”
Gil-Rivera, M., Medina-Gali, R. M., Martínez‐Pinna, J., & Soriano, S. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.02.006 · Cited by 18
Gresch, A., & Düfer, M. (2020) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.265835 · Cited by 13
Self-citationBrouwer, S., Hoffmeister, T., Gresch, A., Schönhoff, L., & Düfer, M. (2018) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700902 · Cited by 11
Self-citationYuan, Y., Wang, H., Jiang, Z.-J., Liu, C., Li, Q., Zhou, S.-R., & Yang, J. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01923-z · Cited by 13
Guzmán, T. J., Klöpper, N., Gurrola‐Díaz, C. M., & Düfer, M. (2024) · Biogerontology · doi:10.1007/s10522-024-10107-9 · Cited by 9
“A proper calcium handling is highly relevant for electrically excitable cells, since the electrical activity is closely coupled to changes in the cytosolic calcium concentrations (Drews et al. 2010).”
BackgroundSelf-citationAdeyemi, W. J., & Olayaki, L. A. (2018) · Synergy · doi:10.1016/j.synres.2018.100045 · Cited by 9
Zhao, Y.-F., Wang, L., Zha, D., Qiao, L., Lu, L.-J., Yu, J., Qu, P., Sun, Q., Qiu, J.-H., & Chen, C. (2013) · Journal of Molecular Endocrinology · doi:10.1530/jme-13-0019 · Cited by 9
“…to generate ATP from ADP, and the increased ATP:ADP ratio closes KATP channels and leads to membrane depolarization and a concomitant rise in the levels of intracellular Ca2C concentration ([Ca2C]i) and insulin secretion (Ashcroft et al. 1994, Rorsman 1997, Drews et al. 2010, Rorsman et al. 2011).”
BackgroundTriton X-100 inhibits L-type voltage-operated calcium channels
Narang, D., Kerr, P. M., Baserman, J., Tam, R., Yang, W., Searle, G. J., Fox, J. E. M., Paulsen, I. M., Kozuska, J. L., MacDonald, P. E., et al. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2012-0257 · Cited by 12
Chloride Channels and Transporters in β-Cell Physiology
Fulvio, M. D., Brown, P. D. N., & Aguilar‐Bryan, L. (2014) · Springer eBooks · doi:10.1007/978-94-007-6686-0_34 · Cited by 4
“Naturally, electrogenic Cl efflux modulates membrane depolarization in response to glucose and therefore stimulates insulin secretion (Best et al. 2010; Drews et al. 2010).”
BackgroundCalamita, G., & Delporte, C. (2023) · Cells · doi:10.3390/cells12172170 · Cited by 9
“The latter allows calcium entry which triggers insulin secretion [288,289].”
BackgroundComparative analysis of reconstructed architectures from mice and human islets
Félix‐Martínez, G. J., & Godínez-Fernández, J. R. (2021) · Islets · doi:10.1080/19382014.2021.1987827 · Cited by 18
Hellman, B., Dansk, H., & Grapengiesser, E. (2018) · Cell Calcium · doi:10.1016/j.ceca.2018.05.007 · Cited by 8
Pajaziti, B., Yosy, K., Steinberg, O. V., & Düfer, M. (2022) · Pflügers Archiv: European Journal of Physiology · doi:10.1007/s00424-022-02772-x · Cited by 6
Self-citation
Metadata
- Authors
- Drews, G., Krippeit-Drews, P., & Düfer, M.
- Affiliations
- University of Tübingen (DE)
- Corresponding author
- Drews, Gisela
- Venue
- Advances in Experimental Medicine and Biology
- Publisher
- Springer Netherlands
- Published
- 2010
- Volume
- 654
- Pages
- 115-163
- ISSN
- 0065-2598 (ISSN-L)
- OpenAlex
- W1886288445
- Cited by
- 152
- References
- 0
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 6 · 2023: 9 · 2022: 8 · 2021: 14 · 2020: 7 · 2019: 4 · 2018: 10 · 2017: 11 · 2016: 4 · 2015: 10 · 2014: 15 · 2013: 16 · 2012: 16
- FWCI
- 135.74
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Advances in experimental medicine and biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Keywords
- pancreatic beta cells, stimulus-secretion coupling, ATP-sensitive potassium channels, beta-cell electrical activity, glucose-stimulated insulin secretion, L-type calcium channels, oxidative stress, alpha cells, delta cells, ion channels, membrane potential, exocytosis, voltage-gated sodium channels
- MeSH terms
- Adenosine Triphosphate, Animals, Calcium, Cell Membrane, Electrophysiology, Glucose, Humans, Ion Channels, Islets of Langerhans, Membrane Potentials, Oscillometry, Potassium Channels, Mice, Knockout, Oxidative Stress, Mice
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