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. 1982 Apr 15;204(1):171–178. doi: 10.1042/bj2040171

The internal pH and membrane potential of the insulin-secretory granule

John C Hutton 1
PMCID: PMC1158329  PMID: 6126183

Abstract

The membrane potential (ΔΨ) and the pH gradient (ΔpH) across the membrane of the insulin-secretory granule were determined in studies in vitro from the uptake of the permeant anion thio[14C]cyanate or the permeant base [14C]methylamine. Freshly prepared granules incubated in iso-osmotic medium containing sucrose and low concentrations of buffer salts exhibited an acidic internal pH and a ΔΨ positive inside. Addition of MgATP2− under these conditions did not alter the ΔpH, but produced a marked increase in the ΔΨ. Conversely, when a permeant anion was also included, ATP produced a marked increase in the ΔpH and a lesser increment in the ΔΨ. NH4+ salts reduced the ΔpH across granule membranes. In the presence of ATP this effect was accompanied by a reciprocal increase in the ΔΨ. A similar reciprocity was evident when nigericin was added together with K+ or on decreasing the medium pH, suggesting that these gradients were linked by a common electrogenic process. The effects of ATP were reversed by the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone, the combination of valinomycin, nigericin and K+, and by the Mg2+-dependent ATPase inhibitor tributyltin. Uptakes of 14C-labelled tracer molecules were also markedly reduced by cryogenic disruption of the granule membrane or hypo-osmotic incubation conditions. These results were readily interpreted within a chemiosmotic hypothesis, which proposed that the insulin granules possess an inwardly-directed electrogenic proton-translocating Mg2+-dependent ATPase with the additional postulate that the membrane has a low proton permeability. The intragranular pH was estimated as being between 5 and 6 in vivo. Such a value corresponds to optimal conditions for the crystallization of zinc–insulin hexamers. Several other functions related to chemiosmotic processes within insulin granules, however, may be envisaged.

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Selected References

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  1. Abrahamsson H., Gylfe E. Demonstration of a proton gradient across the insulin granule membrane. Acta Physiol Scand. 1980 May;109(1):113–114. doi: 10.1111/j.1748-1716.1980.tb06573.x. [DOI] [PubMed] [Google Scholar]
  2. Casey R. P., Njus D., Radda G. K., Sehr P. A. Active proton uptake by chromaffin granules: observation by amine distribution and phosphorus-31 nuclear magnetic resonance techniques. Biochemistry. 1977 Mar 8;16(5):972–977. doi: 10.1021/bi00624a025. [DOI] [PubMed] [Google Scholar]
  3. Chick W. L., Warren S., Chute R. N., Like A. A., Lauris V., Kitchen K. C. A transplantable insulinoma in the rat. Proc Natl Acad Sci U S A. 1977 Feb;74(2):628–632. doi: 10.1073/pnas.74.2.628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Duggan D. E., Pua K. H., Elfenbein G. Purine metabolism in the chick embryo; effects of uricogenesis and xanthine oxidase inhibition. Mol Pharmacol. 1968 Jan;4(1):53–60. [PubMed] [Google Scholar]
  5. Ekholm R., Ericson L. E., Lundquist I. Monoamines in the pancreatic islets of the mouse. Subcellular localization of 5-hydroxytryptamine by electron microscopic autoradiography. Diabetologia. 1971 Oct;7(5):339–348. doi: 10.1007/BF01219468. [DOI] [PubMed] [Google Scholar]
  6. Fletcher D. J., Quigley J. P., Bauer G. E., Noe B. D. Characterization of proinsulin- and proglucagon-converting activities in isolated islet secretory granules. J Cell Biol. 1981 Aug;90(2):312–322. doi: 10.1083/jcb.90.2.312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Herman L., Sato T., Hales C. N. The electron microscopic localization of cations to pancreatic islets of Langerhans and their possible tole in insulin secretion. J Ultrastruct Res. 1973 Feb;42(3):298–311. doi: 10.1016/s0022-5320(73)90058-0. [DOI] [PubMed] [Google Scholar]
  8. Holz R. W. Evidence that catecholamine transport into chromaffin vesicles is coupled to vesicle membrane potential. Proc Natl Acad Sci U S A. 1978 Oct;75(10):5190–5194. doi: 10.1073/pnas.75.10.5190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Howell S. L., Young D. A., Lacy P. E. Isolation and properties of secretory granules from rat islets of Langerhans. 3. Studies of the stability of the isolated beta granules. J Cell Biol. 1969 Apr;41(1):167–176. doi: 10.1083/jcb.41.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hutton J. C., Peshavaria M. Proton-translocating Mg2+-dependent ATPase activity in insulin-secretory granules. Biochem J. 1982 Apr 15;204(1):161–170. doi: 10.1042/bj2040161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Johnson R. G., Scarpa A., Salganicoff L. The internal pH of isolated serotonin containing granules of pig platelets. J Biol Chem. 1978 Oct 10;253(19):7061–7068. [PubMed] [Google Scholar]
  12. Kohnert K. D., Hahn H. J., Gylfe E., Borg H., Hellman B. Calcium and pancreatic beta-cell function. 6. Glucose and intracellular 45Ca distribution. Mol Cell Endocrinol. 1979 Dec;16(3):205–220. doi: 10.1016/0303-7207(79)90027-3. [DOI] [PubMed] [Google Scholar]
  13. Njus D., Radda G. K. A potassium ion diffusion potential causes adrenaline uptake in chromaffin-granule 'ghosts'. Biochem J. 1979 Jun 15;180(3):579–585. doi: 10.1042/bj1800579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Njus D., Radda G. K. Bioenergetic processes in chromaffin granules a new perspective on some old problems. Biochim Biophys Acta. 1978 Mar 10;463(3-4):219–244. doi: 10.1016/0304-4173(78)90001-0. [DOI] [PubMed] [Google Scholar]
  15. Poisner A. M., Trifaró J. M. The role of ATP and ATPase in the release of catecholamines from the adrenal medulla. I. ATP-evoked release of catecholamines, ATP, and protein from isolated chromaffin granules. Mol Pharmacol. 1967 Nov;3(6):561–571. [PubMed] [Google Scholar]
  16. Roos A., Boron W. F. Intracellular pH. Physiol Rev. 1981 Apr;61(2):296–434. doi: 10.1152/physrev.1981.61.2.296. [DOI] [PubMed] [Google Scholar]
  17. Rottenberg H. The measurement of membrane potential and deltapH in cells, organelles, and vesicles. Methods Enzymol. 1979;55:547–569. doi: 10.1016/0076-6879(79)55066-6. [DOI] [PubMed] [Google Scholar]
  18. Russell J. T., Holz R. W. Measurement of delta pH and membrane potential in isolated neurosecretory vesicles from bovine neurohypophyses. J Biol Chem. 1981 Jun 25;256(12):5950–5953. [PubMed] [Google Scholar]
  19. Sener A., Hutton J. C., Kawazu S., Boschero A. C., Somers G., Devis G., Herchuelz A., Malaisse W. J. The stimulus-secretion coupling of glucose-induced insulin release. Metabolic and functional effects of NH4+ in rat islets. J Clin Invest. 1978 Oct;62(4):868–878. doi: 10.1172/JCI109199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Stockdale M., Dawson A. P., Selwyn M. J. Effects of trialkyltin and triphenyltin compounds on mitochondrial respiration. Eur J Biochem. 1970 Aug;15(2):342–351. doi: 10.1111/j.1432-1033.1970.tb01013.x. [DOI] [PubMed] [Google Scholar]
  21. Wilkins J. A., Salganicoff L. Participation of a transmembrane proton gradient in 5-hydroxytryptamine transport by platelet dense granules and dense-granule ghosts. Biochem J. 1981 Jul 15;198(1):113–123. doi: 10.1042/bj1980113. [DOI] [PMC free article] [PubMed] [Google Scholar]

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