Abstract
The reverse hemolytic plaque assay (RHPA) was used to study the secretory properties of single rat pancreatic B cells, and to identify insulin-secreting cells for patch-clamp experiments. In secretion studies using the RHPA, we find that the percentage of secreting B cells and the amount of insulin secreted per B cell increase as the glucose concentration is raised from 0 to 20 mM. Using the whole-cell variation of the patch-clamp technique, we find that identified B cells have three types of channels capable of carrying inward current: (a) tetrodotoxin-sensitive, voltage-dependent Na channels, which are nearly completely inactivated at -40 mV, (b) fast deactivating (FD) Ca channels, and (c) slowly deactivating (SD) Ca channels. We have shown that Na channels are functionally significant to the B cell, because tetrodotoxin partially inhibits glucose-induced insulin secretion. The properties of FD and SD Ca channels differ in several respects. FD channels deactivate at -80 mV, with a time constant of 129 microseconds, they are half-maximally activated near +15 mV, they do not inactivate during 100 ms, they conduct Ba2+ better than Ca2+, and they are very sensitive to washout during intracellular dialysis. SD channels, on the other hand, deactivate with a time constant of 2.8 ms, they are half-maximally activated near -5 mV, they inactivate rapidly, they conduct Ba2+ and Ca2+ equally well, and they are insensitive to washout.
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Selected References
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- Armstrong C. M., Bezanilla F. Charge movement associated with the opening and closing of the activation gates of the Na channels. J Gen Physiol. 1974 May;63(5):533–552. doi: 10.1085/jgp.63.5.533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Armstrong C. M., Matteson D. R. Two distinct populations of calcium channels in a clonal line of pituitary cells. Science. 1985 Jan 4;227(4682):65–67. doi: 10.1126/science.2578071. [DOI] [PubMed] [Google Scholar]
- Ashcroft F. M., Harrison D. E., Ashcroft S. J. Glucose induces closure of single potassium channels in isolated rat pancreatic beta-cells. 1984 Nov 29-Dec 5Nature. 312(5993):446–448. doi: 10.1038/312446a0. [DOI] [PubMed] [Google Scholar]
- Ashcroft S. J., Bassett J. M., Randle P. J. Insulin secretion mechanisms and glucose metabolism in isolated islets. Diabetes. 1972;21(2 Suppl):538–545. [PubMed] [Google Scholar]
- Bean B. P. Two kinds of calcium channels in canine atrial cells. Differences in kinetics, selectivity, and pharmacology. J Gen Physiol. 1985 Jul;86(1):1–30. doi: 10.1085/jgp.86.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carbone E., Lux H. D. A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neurones. Nature. 1984 Aug 9;310(5977):501–502. doi: 10.1038/310501a0. [DOI] [PubMed] [Google Scholar]
- Cook D. L., Crill W. E., Porte D., Jr Plateau potentials in pancreatic islet cells are voltage-dependent action potentials. Nature. 1980 Jul 24;286(5771):404–406. doi: 10.1038/286404a0. [DOI] [PubMed] [Google Scholar]
- Cook D. L., Ikeuchi M., Fujimoto W. Y. Lowering of pHi inhibits Ca2+-activated K+ channels in pancreatic B-cells. Nature. 1984 Sep 20;311(5983):269–271. doi: 10.1038/311269a0. [DOI] [PubMed] [Google Scholar]
- Cota G. Calcium channel currents in pars intermedia cells of the rat pituitary gland. Kinetic properties and washout during intracellular dialysis. J Gen Physiol. 1986 Jul;88(1):83–105. doi: 10.1085/jgp.88.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dean P. M., Matthews E. K. Electrical activity in pancreatic islet cells. Nature. 1968 Jul 27;219(5152):389–390. doi: 10.1038/219389a0. [DOI] [PubMed] [Google Scholar]
- Dean P. M., Matthews E. K. Glucose-induced electrical activity in pancreatic islet cells. J Physiol. 1970 Sep;210(2):255–264. doi: 10.1113/jphysiol.1970.sp009207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dean P. M., Matthews E. K., Sakamoto Y. Pancreatic islet cells: effects of monosaccharides, glycolytic intermediates and metabolic inhibitors on membrane potential and electrical activity. J Physiol. 1975 Mar;246(2):459–478. doi: 10.1113/jphysiol.1975.sp010899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Donatsch P., Lowe D. A., Richardson B. P., Taylor P. The functional significance of sodium channels in pancreatic beta-cell membranes. J Physiol. 1977 May;267(2):357–376. doi: 10.1113/jphysiol.1977.sp011817. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Findlay I., Dunne M. J. Voltage-activated Ca2+ currents in insulin-secreting cells. FEBS Lett. 1985 Sep 23;189(2):281–285. doi: 10.1016/0014-5793(85)81040-1. [DOI] [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]
- Kass R. S., Krafte D. S. Negative surface charge density near heart calcium channels. Relevance to block by dihydropyridines. J Gen Physiol. 1987 Apr;89(4):629–644. doi: 10.1085/jgp.89.4.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kostyuk P. G. Metabolic control of ionic channels in the neuronal membrane. Neuroscience. 1984 Dec;13(4):983–989. doi: 10.1016/0306-4522(84)90282-3. [DOI] [PubMed] [Google Scholar]
- Lacy P. E., Kostianovsky M. Method for the isolation of intact islets of Langerhans from the rat pancreas. Diabetes. 1967 Jan;16(1):35–39. doi: 10.2337/diab.16.1.35. [DOI] [PubMed] [Google Scholar]
- Lingle C. J., Sombati S., Freeman M. E. Membrane currents in identified lactotrophs of rat anterior pituitary. J Neurosci. 1986 Oct;6(10):2995–3005. doi: 10.1523/JNEUROSCI.06-10-02995.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Malaisse W. J., Malaisse-Lagae F. The role of cyclic AMP in insulin release. Experientia. 1984 Oct 15;40(10):1068–1074. doi: 10.1007/BF01971453. [DOI] [PubMed] [Google Scholar]
- Matteson D. R., Armstrong C. M. Na and Ca channels in a transformed line of anterior pituitary cells. J Gen Physiol. 1984 Mar;83(3):371–394. doi: 10.1085/jgp.83.3.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matteson D. R., Armstrong C. M. Properties of two types of calcium channels in clonal pituitary cells. J Gen Physiol. 1986 Jan;87(1):161–182. doi: 10.1085/jgp.87.1.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meda P., Hooghe-Peters E. L., Orci L. Monolayer cultures of adult pancreatic islet cells on osmotically disrupted fibroblasts. Diabetes. 1980 Jun;29(6):497–500. doi: 10.2337/diab.29.6.497. [DOI] [PubMed] [Google Scholar]
- Meissner H. P., Atwater I. J. The kinetics of electrical activity of beta cells in response to a "square wave" stimulation with glucose or glibenclamide. Horm Metab Res. 1976 Jan;8(1):11–16. doi: 10.1055/s-0028-1093685. [DOI] [PubMed] [Google Scholar]
- Meissner H. P. Electrical characteristics of the beta-cells in pancreatic islets. J Physiol (Paris) 1976 Nov;72(6):757–767. [PubMed] [Google Scholar]
- Meissner H. P., Schmelz H. Membrane potential of beta-cells in pancreatic islets. Pflugers Arch. 1974;351(3):195–206. doi: 10.1007/BF00586918. [DOI] [PubMed] [Google Scholar]
- Misler S., Falke L. C., Gillis K., McDaniel M. L. A metabolite-regulated potassium channel in rat pancreatic B cells. Proc Natl Acad Sci U S A. 1986 Sep;83(18):7119–7123. doi: 10.1073/pnas.83.18.7119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Narahashi T., Tsunoo A., Yoshii M. Characterization of two types of calcium channels in mouse neuroblastoma cells. J Physiol. 1987 Feb;383:231–249. doi: 10.1113/jphysiol.1987.sp016406. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neill J. D., Frawley L. S. Detection of hormone release from individual cells in mixed populations using a reverse hemolytic plaque assay. Endocrinology. 1983 Mar;112(3):1135–1137. doi: 10.1210/endo-112-3-1135. [DOI] [PubMed] [Google Scholar]
- Nilius B., Hess P., Lansman J. B., Tsien R. W. A novel type of cardiac calcium channel in ventricular cells. Nature. 1985 Aug 1;316(6027):443–446. doi: 10.1038/316443a0. [DOI] [PubMed] [Google Scholar]
- Nowycky M. C., Fox A. P., Tsien R. W. Three types of neuronal calcium channel with different calcium agonist sensitivity. Nature. 1985 Aug 1;316(6027):440–443. doi: 10.1038/316440a0. [DOI] [PubMed] [Google Scholar]
- Ozawa S., Sand O. Electrophysiology of excitable endocrine cells. Physiol Rev. 1986 Oct;66(4):887–952. doi: 10.1152/physrev.1986.66.4.887. [DOI] [PubMed] [Google Scholar]
- Pace C. S. Activation of Na channels in islet cells: metabolic and secretory effects. Am J Physiol. 1979 Aug;237(2):E130–E135. doi: 10.1152/ajpendo.1979.237.2.E130. [DOI] [PubMed] [Google Scholar]
- Ribalet B., Beigelman P. M. Calcium action potentials and potassium permeability activation in pancreatic beta-cells. Am J Physiol. 1980 Sep;239(3):C124–C133. doi: 10.1152/ajpcell.1980.239.3.C124. [DOI] [PubMed] [Google Scholar]
- Ribalet B., Beigelman P. M. Effects of sodium on beta-cell electrical activity. Am J Physiol. 1982 May;242(5):C296–C303. doi: 10.1152/ajpcell.1982.242.5.C296. [DOI] [PubMed] [Google Scholar]
- Rorsman P., Arkhammar P., Berggren P. O. Voltage-activated Na+ currents and their suppression by phorbol ester in clonal insulin-producing RINm5F cells. Am J Physiol. 1986 Dec;251(6 Pt 1):C912–C919. doi: 10.1152/ajpcell.1986.251.6.C912. [DOI] [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]
- Salomon D., Meda P. Heterogeneity and contact-dependent regulation of hormone secretion by individual B cells. Exp Cell Res. 1986 Feb;162(2):507–520. doi: 10.1016/0014-4827(86)90354-x. [DOI] [PubMed] [Google Scholar]
- Satin L. S., Cook D. L. Voltage-gated Ca2+ current in pancreatic B-cells. Pflugers Arch. 1985 Aug;404(4):385–387. doi: 10.1007/BF00585354. [DOI] [PubMed] [Google Scholar]
- Smith P. F., Luque E. H., Neill J. D. Detection and measurement of secretion from individual neuroendocrine cells using a reverse hemolytic plaque assay. Methods Enzymol. 1986;124:443–465. doi: 10.1016/0076-6879(86)24034-3. [DOI] [PubMed] [Google Scholar]
