Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1992 Oct 2;119(2):313–324. doi: 10.1083/jcb.119.2.313

Immunocytochemical localization of alpha-protein kinase C in rat pancreatic beta-cells during glucose-induced insulin secretion

PMCID: PMC2289651  PMID: 1400576

Abstract

To investigate the role of protein kinase C (PKC) in the regulation of insulin secretion, we visualized changes in the intracellular localization of alpha-PKC in fixed beta-cells from both isolated rat pancreatic islets and the pancreas of awake unstressed rats during glucose-induced insulin secretion. Isolated, perifused rat islets were fixed in 4% paraformaldehyde, detergent permeabilized, and labeled with a mAb specific for alpha-PKC. The labeling was visualized by confocal immunofluorescent microscopy. In isolated rat pancreatic islets perifused with 2.75 mM glucose, alpha-PKC immunostaining was primarily cytoplasmic in distribution throughout the beta-cells. In islets stimulated with 20 mM glucose, there was a significant redistribution of alpha-PKC to the cell periphery. This glucose-induced redistribution was abolished when either mannoheptulose, an inhibitor of glucose metabolism, or nitrendipine, an inhibitor of calcium influx, were added to the perifusate. We also examined changes in the intracellular distribution of alpha-PKC in the beta-cells of awake, unstressed rats that were given an intravenous infusion of glucose. Immunocytochemical analysis of pancreatic sections from these rats demonstrated a glucose- induced translocation of alpha-PKC to the cell periphery of the beta- cells. These results demonstrate that the metabolism of glucose can induce the redistribution of alpha-PKC to the cell periphery of beta- cells, both in isolated islets and in the intact animal, and suggest that alpha-PKC plays a role in mediating glucose-induced insulin secretion.

Full Text

The Full Text of this article is available as a PDF (4.4 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Albano J. D., Ekins R. P., Maritz G., Turner R. C. A sensitive, precise radioimmunoassay of serum insulin relying on charcoal separation of bound and free hormone moieties. Acta Endocrinol (Copenh) 1972 Jul;70(3):487–509. doi: 10.1530/acta.0.0700487. [DOI] [PubMed] [Google Scholar]
  2. Arkhammar P., Nilsson T., Rorsman P., Berggren P. O. Inhibition of ATP-regulated K+ channels precedes depolarization-induced increase in cytoplasmic free Ca2+ concentration in pancreatic beta-cells. J Biol Chem. 1987 Apr 25;262(12):5448–5454. [PubMed] [Google Scholar]
  3. Ashcroft S. J., Weerasinghe L. C., Randle P. J. Interrelationship of islet metabolism, adenosine triphosphate content and insulin release. Biochem J. 1973 Feb;132(2):223–231. doi: 10.1042/bj1320223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Best L. A role for calcium in the breakdown of inositol phospholipids in intact and digitonin-permeabilized pancreatic islets. Biochem J. 1986 Sep 15;238(3):773–779. doi: 10.1042/bj2380773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Calle R., Ganesan S., Smallwood J. I., Rasmussen H. Glucose-induced phosphorylation of myristoylated alanine-rich C kinase substrate (MARCKS) in isolated rat pancreatic islets. J Biol Chem. 1992 Sep 15;267(26):18723–18727. [PubMed] [Google Scholar]
  6. Cook D. L., Satin L. S., Ashford M. L., Hales C. N. ATP-sensitive K+ channels in pancreatic beta-cells. Spare-channel hypothesis. Diabetes. 1988 May;37(5):495–498. doi: 10.2337/diab.37.5.495. [DOI] [PubMed] [Google Scholar]
  7. Coore H. G., Randle P. J. Inhibition of glucose phosphorylation by mannoheptulose. Biochem J. 1964 Apr;91(1):56–59. doi: 10.1042/bj0910056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Curry D. L., Bennett L. L., Grodsky G. M. Dynamics of insulin secretion by the perfused rat pancreas. Endocrinology. 1968 Sep;83(3):572–584. doi: 10.1210/endo-83-3-572. [DOI] [PubMed] [Google Scholar]
  9. Easom R. A., Hughes J. H., Landt M., Wolf B. A., Turk J., McDaniel M. L. Comparison of effects of phorbol esters and glucose on protein kinase C activation and insulin secretion in pancreatic islets. Biochem J. 1989 Nov 15;264(1):27–33. doi: 10.1042/bj2640027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Easom R. A., Landt M., Colca J. R., Hughes J. H., Turk J., McDaniel M. Effects of insulin secretagogues on protein kinase C-catalyzed phosphorylation of an endogenous substrate in isolated pancreatic islets. J Biol Chem. 1990 Sep 5;265(25):14938–14946. [PubMed] [Google Scholar]
  11. Ganesan S., Calle R., Zawalich K., Smallwood J. I., Zawalich W. S., Rasmussen H. Glucose-induced translocation of protein kinase C in rat pancreatic islets. Proc Natl Acad Sci U S A. 1990 Dec;87(24):9893–9897. doi: 10.1073/pnas.87.24.9893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gerich J. E., Charles M. A., Grodsky G. M. Characterization of the effects of arginine and glucose on glucagon and insulin release from the perfused rat pancreas. J Clin Invest. 1974 Oct;54(4):833–841. doi: 10.1172/JCI107823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Grill V., Adamson U., Cerasi E. Immediate and time-dependent effects of glucose on insulin release from rat pancreatic tissue. Evidence for different mechanisms of action. J Clin Invest. 1978 Apr;61(4):1034–1043. doi: 10.1172/JCI109002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hidaka H., Tanaka T., Onoda K., Hagiwara M., Watanabe M., Ohta H., Ito Y., Tsurudome M., Yoshida T. Cell type-specific expression of protein kinase C isozymes in the rabbit cerebellum. J Biol Chem. 1988 Apr 5;263(10):4523–4526. [PubMed] [Google Scholar]
  15. Ito T., Tanaka T., Yoshida T., Onoda K., Ohta H., Hagiwara M., Itoh Y., Ogura M., Saito H., Hidaka H. Immunocytochemical evidence for translocation of protein kinase C in human megakaryoblastic leukemic cells: synergistic effects of Ca2+ and activators of protein kinase C on the plasma membrane association. J Cell Biol. 1988 Sep;107(3):929–937. doi: 10.1083/jcb.107.3.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Jaken S., Leach K., Klauck T. Association of type 3 protein kinase C with focal contacts in rat embryo fibroblasts. J Cell Biol. 1989 Aug;109(2):697–704. doi: 10.1083/jcb.109.2.697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Karlsson S., Ahrén B. Cholecystokinin-stimulated insulin secretion and protein kinase C in rat pancreatic islets. Acta Physiol Scand. 1991 Jul;142(3):397–403. doi: 10.1111/j.1748-1716.1991.tb09173.x. [DOI] [PubMed] [Google Scholar]
  18. Kiekens R., In 't Veld P., Mahler T., Schuit F., Van De Winkel M., Pipeleers D. Differences in glucose recognition by individual rat pancreatic B cells are associated with intercellular differences in glucose-induced biosynthetic activity. J Clin Invest. 1992 Jan;89(1):117–125. doi: 10.1172/JCI115551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Leach K. L., Powers E. A., Ruff V. A., Jaken S., Kaufmann S. Type 3 protein kinase C localization to the nuclear envelope of phorbol ester-treated NIH 3T3 cells. J Cell Biol. 1989 Aug;109(2):685–695. doi: 10.1083/jcb.109.2.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Matschinsky F. M. Glucokinase as glucose sensor and metabolic signal generator in pancreatic beta-cells and hepatocytes. Diabetes. 1990 Jun;39(6):647–652. doi: 10.2337/diab.39.6.647. [DOI] [PubMed] [Google Scholar]
  21. Metz S. A. Perspectives in diabetes. Is protein kinase C required for physiologic insulin release? Diabetes. 1988 Jan;37(1):3–7. doi: 10.2337/diab.37.1.3. [DOI] [PubMed] [Google Scholar]
  22. Mochly-Rosen D., Henrich C. J., Cheever L., Khaner H., Simpson P. C. A protein kinase C isozyme is translocated to cytoskeletal elements on activation. Cell Regul. 1990 Aug;1(9):693–706. doi: 10.1091/mbc.1.9.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Mochly-Rosen D., Khaner H., Lopez J., Smith B. L. Intracellular receptors for activated protein kinase C. Identification of a binding site for the enzyme. J Biol Chem. 1991 Aug 15;266(23):14866–14868. [PubMed] [Google Scholar]
  24. Nishizuka Y. Studies and perspectives of protein kinase C. Science. 1986 Jul 18;233(4761):305–312. doi: 10.1126/science.3014651. [DOI] [PubMed] [Google Scholar]
  25. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988 Aug 25;334(6184):661–665. doi: 10.1038/334661a0. [DOI] [PubMed] [Google Scholar]
  26. Onoda K., Hagiwara M., Hachiya T., Usuda N., Nagata T., Hidaka H. Different expression of protein kinase C isozymes in pancreatic islet cells. Endocrinology. 1990 Feb;126(2):1235–1240. doi: 10.1210/endo-126-2-1235. [DOI] [PubMed] [Google Scholar]
  27. Persaud S. J., Jones P. M., Howell S. L. Activation of protein kinase C is essential for sustained insulin secretion in response to cholinergic stimulation. Biochim Biophys Acta. 1991 Jan 10;1091(1):120–122. doi: 10.1016/0167-4889(91)90231-l. [DOI] [PubMed] [Google Scholar]
  28. Persaud S. J., Jones P. M., Sugden D., Howell S. L. Translocation of protein kinase C in rat islets of Langerhans. Effects of a phorbol ester, carbachol and glucose. FEBS Lett. 1989 Mar 13;245(1-2):80–84. doi: 10.1016/0014-5793(89)80196-6. [DOI] [PubMed] [Google Scholar]
  29. Peter-Riesch B., Fathi M., Schlegel W., Wollheim C. B. Glucose and carbachol generate 1,2-diacylglycerols by different mechanisms in pancreatic islets. J Clin Invest. 1988 Apr;81(4):1154–1161. doi: 10.1172/JCI113430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Prentki M., Matschinsky F. M. Ca2+, cAMP, and phospholipid-derived messengers in coupling mechanisms of insulin secretion. Physiol Rev. 1987 Oct;67(4):1185–1248. doi: 10.1152/physrev.1987.67.4.1185. [DOI] [PubMed] [Google Scholar]
  31. Rasmussen H., Zawalich K. C., Ganesan S., Calle R., Zawalich W. S. Physiology and pathophysiology of insulin secretion. Diabetes Care. 1990 Jun;13(6):655–666. doi: 10.2337/diacare.13.6.655. [DOI] [PubMed] [Google Scholar]
  32. Turk J., Wolf B. A., McDaniel M. L. Glucose-induced accumulation of inositol trisphosphates in isolated pancreatic islets. Predominance of the 1,3,4-isomer. Biochem J. 1986 Jul 1;237(1):259–263. doi: 10.1042/bj2370259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wollheim C. B., Regazzi R. Protein kinase C in insulin releasing cells. Putative role in stimulus secretion coupling. FEBS Lett. 1990 Aug 1;268(2):376–380. doi: 10.1016/0014-5793(90)81289-z. [DOI] [PubMed] [Google Scholar]
  34. 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]
  35. Zawalich W. S., Dye E. S., Rognstad R., Matschinsky F. M. On the biochemical nature of triose- and hexose-stimulated insulin secretion. Endocrinology. 1978 Dec;103(6):2027–2034. doi: 10.1210/endo-103-6-2027. [DOI] [PubMed] [Google Scholar]
  36. Zawalich W. S., Rasmussen H. Control of insulin secretion: a model involving Ca2+, cAMP and diacylglycerol. Mol Cell Endocrinol. 1990 Apr 17;70(2):119–137. doi: 10.1016/0303-7207(90)90152-x. [DOI] [PubMed] [Google Scholar]
  37. Zawalich W. S., Zawalich K. C., Ganesan S., Calle R., Rasmussen H. Influence of staurosporine on glucose-mediated and glucose-conditioned insulin secretion. Biochem J. 1991 Nov 1;279(Pt 3):807–813. doi: 10.1042/bj2790807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Zawalich W. S., Zawalich K. C. Phosphoinositide hydrolysis and insulin release from isolated perifused rat islets. Studies with glucose. Diabetes. 1988 Sep;37(9):1294–1300. doi: 10.2337/diab.37.9.1294. [DOI] [PubMed] [Google Scholar]
  39. Zawalich W., Brown C., Rasmussen H. Insulin secretion: combined effects of phorbol ester and A23187. Biochem Biophys Res Commun. 1983 Dec 16;117(2):448–455. doi: 10.1016/0006-291x(83)91221-4. [DOI] [PubMed] [Google Scholar]
  40. Zawalich W., Zawalich K., Rasmussen H. Insulin secretion: combined tolbutamide, forskolin and TPA mimic action of glucose. Cell Calcium. 1984 Dec;5(6):551–558. doi: 10.1016/0143-4160(84)90031-9. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES