Abstract
1. The mechanisms by which cooling inhibits insulin secretion were investigated by capacitance measurements of exocytosis in single mouse pancreatic B-cells maintained in short-term tissue culture. 2. A reduction of the bath temperature from 34 to 24 degrees C produced a gradual inhibition of exocytosis. Inhibition of exocytosis was use dependent rather than time dependent. The steady-state inhibition amounted to 90%, which was paralleled by a 30% reduction of the peak Ca2+ current. 3. The Q10 values (between 27 and 37 degrees C) for inhibition of exocytosis and the peak Ca2+ current amplitude were determined as > 5 and 1.6, respectively. From the temperature dependence of exocytosis, an energy of activation was estimated as 145 kJ mol-1. 4. Suppression of exocytosis was not the result of a reduction of Ca2+ influx. When the Ca2+ currents were blocked by 30% (comparable to that produced by cooling) by using a low concentration of Co2+, exocytosis was reduced by < 25%. 5. Elevation of cytoplasmic free Ca2+, by photorelease of 'caged' Ca2+ from Ca(2+)-nitrophenyl-EGTA preloaded into the B-cell, was equally effective at eliciting exocytosis at 24 and 34 degrees C. 6. Cooling produced 70% inhibition of exocytosis evoked by infusion of Ca2+ through the recording electrode. Omission of either MgATP or cAMP from the electrode solution resulted in a comparable reduction of exocytosis. Cooling had no additional inhibitory effect when exocytosis was already suppressed by removal of cytoplasmic MgATP. 7. Our data indicate that exocytosis of granules already docked beneath the membrane is little affected by cooling in the B-cell. Instead, the high overall temperature sensitivity of insulin secretion arises because the replenishment of the readily releasable pool is temperature dependent.
Full text
PDF











Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ammälä C., Ashcroft F. M., Rorsman P. Calcium-independent potentiation of insulin release by cyclic AMP in single beta-cells. Nature. 1993 May 27;363(6427):356–358. doi: 10.1038/363356a0. [DOI] [PubMed] [Google Scholar]
- Ammälä C., Eliasson L., Bokvist K., Larsson O., Ashcroft F. M., Rorsman P. Exocytosis elicited by action potentials and voltage-clamp calcium currents in individual mouse pancreatic B-cells. J Physiol. 1993 Dec;472:665–688. doi: 10.1113/jphysiol.1993.sp019966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Atwater I., Goncalves A., Herchuelz A., Lebrun P., Malaisse W. J., Rojas E., Scott A. Cooling dissociates glucose-induced insulin release from electrical activity and cation fluxes in rodent pancreatic islets. J Physiol. 1984 Mar;348:615–627. doi: 10.1113/jphysiol.1984.sp015129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Augustine G. J., Neher E. Calcium requirements for secretion in bovine chromaffin cells. J Physiol. 1992 May;450:247–271. doi: 10.1113/jphysiol.1992.sp019126. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bittner M. A., Holz R. W. A temperature-sensitive step in exocytosis. J Biol Chem. 1992 Aug 15;267(23):16226–16229. [PubMed] [Google Scholar]
- Bokvist K., Eliasson L., Ammälä C., Renström E., Rorsman P. Co-localization of L-type Ca2+ channels and insulin-containing secretory granules and its significance for the initiation of exocytosis in mouse pancreatic B-cells. EMBO J. 1995 Jan 3;14(1):50–57. doi: 10.1002/j.1460-2075.1995.tb06974.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burgoyne R. D., Morgan A. Regulated exocytosis. Biochem J. 1993 Jul 15;293(Pt 2):305–316. doi: 10.1042/bj2930305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Byerly L., Chase P. B., Stimers J. R. Calcium current activation kinetics in neurones of the snail Lymnaea stagnalis. J Physiol. 1984 Mar;348:187–207. doi: 10.1113/jphysiol.1984.sp015105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dean P. M. Ultrastructural morphometry of the pancreatic -cell. Diabetologia. 1973 Apr;9(2):115–119. doi: 10.1007/BF01230690. [DOI] [PubMed] [Google Scholar]
- Detimary P., Gilon P., Nenquin M., Henquin J. C. Two sites of glucose control of insulin release with distinct dependence on the energy state in pancreatic B-cells. Biochem J. 1994 Feb 1;297(Pt 3):455–461. doi: 10.1042/bj2970455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ellis-Davies G. C., Kaplan J. H. Nitrophenyl-EGTA, a photolabile chelator that selectively binds Ca2+ with high affinity and releases it rapidly upon photolysis. Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):187–191. doi: 10.1073/pnas.91.1.187. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gembal M., Detimary P., Gilon P., Gao Z. Y., Henquin J. C. Mechanisms by which glucose can control insulin release independently from its action on adenosine triphosphate-sensitive K+ channels in mouse B cells. J Clin Invest. 1993 Mar;91(3):871–880. doi: 10.1172/JCI116308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gillis K. D., Misler S. Enhancers of cytosolic cAMP augment depolarization-induced exocytosis from pancreatic B-cells: evidence for effects distal to Ca2+ entry. Pflugers Arch. 1993 Jul;424(2):195–197. doi: 10.1007/BF00374612. [DOI] [PubMed] [Google Scholar]
- Gillis K. D., Misler S. Single cell assay of exocytosis from pancreatic islet B cells. Pflugers Arch. 1992 Jan;420(1):121–123. doi: 10.1007/BF00378654. [DOI] [PubMed] [Google Scholar]
- Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
- Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
- Horn R., Marty A. Muscarinic activation of ionic currents measured by a new whole-cell recording method. J Gen Physiol. 1988 Aug;92(2):145–159. doi: 10.1085/jgp.92.2.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Iatridou H., Foukaraki E., Kuhn M. A., Marcus E. M., Haugland R. P., Katerinopoulos H. E. The development of a new family of intracellular calcium probes. Cell Calcium. 1994 Feb;15(2):190–198. doi: 10.1016/0143-4160(94)90058-2. [DOI] [PubMed] [Google Scholar]
- Joshi C., Fernandez J. M. Capacitance measurements. An analysis of the phase detector technique used to study exocytosis and endocytosis. Biophys J. 1988 Jun;53(6):885–892. doi: 10.1016/S0006-3495(88)83169-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Knight D. E., Baker P. F. Calcium-dependence of catecholamine release from bovine adrenal medullary cells after exposure to intense electric fields. J Membr Biol. 1982;68(2):107–140. doi: 10.1007/BF01872259. [DOI] [PubMed] [Google Scholar]
- Knight D. E., Baker P. F. Stimulus-secretion coupling in isolated bovine adrenal medullary cells. Q J Exp Physiol. 1983 Jan;68(1):123–143. doi: 10.1113/expphysiol.1983.sp002691. [DOI] [PubMed] [Google Scholar]
- Lim N. F., Nowycky M. C., Bookman R. J. Direct measurement of exocytosis and calcium currents in single vertebrate nerve terminals. Nature. 1990 Mar 29;344(6265):449–451. doi: 10.1038/344449a0. [DOI] [PubMed] [Google Scholar]
- Loubatieres-Mariani M. M., Chapa J., Puech R., Manteghetti M. A different action of hypothermia on insulin release from the isolated, perfused rat pancreas, depending on the stimulating agent. Diabetes. 1980 Nov;29(11):895–898. doi: 10.2337/diab.29.11.895. [DOI] [PubMed] [Google Scholar]
- Loubatières-Mariani M. M., Chapal J., Puech R., Lignon F., Valette G. Different effects of hypothermia on insulin and glucagon secretion from the isolated perfused rat pancreas. Diabetologia. 1980 Apr;18(4):329–333. doi: 10.1007/BF00251015. [DOI] [PubMed] [Google Scholar]
- Matsumoto K., Fukunaga K., Miyazaki J., Shichiri M., Miyamoto E. Ca2+/calmodulin-dependent protein kinase II and synapsin I-like protein in mouse insulinoma MIN6 cells. Endocrinology. 1995 Sep;136(9):3784–3793. doi: 10.1210/endo.136.9.7649085. [DOI] [PubMed] [Google Scholar]
- Neher E., Zucker R. S. Multiple calcium-dependent processes related to secretion in bovine chromaffin cells. Neuron. 1993 Jan;10(1):21–30. doi: 10.1016/0896-6273(93)90238-m. [DOI] [PubMed] [Google Scholar]
- Nobile M., Carbone E., Lux H. D., Zucker H. Temperature sensitivity of Ca currents in chick sensory neurones. Pflugers Arch. 1990 Mar;415(6):658–663. doi: 10.1007/BF02584002. [DOI] [PubMed] [Google Scholar]
- Ohta M., Nelson D., Nelson J., Meglasson M. D., Erecińska M. Oxygen and temperature dependence of stimulated insulin secretion in isolated rat islets of Langerhans. J Biol Chem. 1990 Oct 15;265(29):17525–17532. [PubMed] [Google Scholar]
- Orci L., Gabbay K. H., Malaisse W. J. Pancreatic beta-cell web: its possible role in insulin secretion. Science. 1972 Mar 10;175(4026):1128–1130. doi: 10.1126/science.175.4026.1128. [DOI] [PubMed] [Google Scholar]
- Parsons T. D., Coorssen J. R., Horstmann H., Almers W. Docked granules, the exocytic burst, and the need for ATP hydrolysis in endocrine cells. Neuron. 1995 Nov;15(5):1085–1096. doi: 10.1016/0896-6273(95)90097-7. [DOI] [PubMed] [Google Scholar]
- Rae J., Cooper K., Gates P., Watsky M. Low access resistance perforated patch recordings using amphotericin B. J Neurosci Methods. 1991 Mar;37(1):15–26. doi: 10.1016/0165-0270(91)90017-t. [DOI] [PubMed] [Google Scholar]
- Rorsman P., Ammälä C., Berggren P. O., Bokvist K., Larsson O. Cytoplasmic calcium transients due to single action potentials and voltage-clamp depolarizations in mouse pancreatic B-cells. EMBO J. 1992 Aug;11(8):2877–2884. doi: 10.1002/j.1460-2075.1992.tb05356.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rorsman P., Trube G. Calcium and delayed potassium currents in mouse pancreatic beta-cells under voltage-clamp conditions. J Physiol. 1986 May;374:531–550. doi: 10.1113/jphysiol.1986.sp016096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sihra T. S., Wang J. K., Gorelick F. S., Greengard P. Translocation of synapsin I in response to depolarization of isolated nerve terminals. Proc Natl Acad Sci U S A. 1989 Oct;86(20):8108–8112. doi: 10.1073/pnas.86.20.8108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas P., Surprenant A., Almers W. Cytosolic Ca2+, exocytosis, and endocytosis in single melanotrophs of the rat pituitary. Neuron. 1990 Nov;5(5):723–733. doi: 10.1016/0896-6273(90)90226-6. [DOI] [PubMed] [Google Scholar]
- Thomas P., Wong J. G., Lee A. K., Almers W. A low affinity Ca2+ receptor controls the final steps in peptide secretion from pituitary melanotrophs. Neuron. 1993 Jul;11(1):93–104. doi: 10.1016/0896-6273(93)90274-u. [DOI] [PubMed] [Google Scholar]
- Wollheim C. B., Sharp G. W. Regulation of insulin release by calcium. Physiol Rev. 1981 Oct;61(4):914–973. doi: 10.1152/physrev.1981.61.4.914. [DOI] [PubMed] [Google Scholar]
- van Lunteren E., Elmslie K. S., Jones S. W. Effects of temperature on calcium current of bullfrog sympathetic neurons. J Physiol. 1993 Jul;466:81–93. [PMC free article] [PubMed] [Google Scholar]
