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Regulation of exocytosis in electrically permeabilized insulin-secreting cells. Evidence for Ca2+ dependent and independent secretion

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Bioscience Reports

Abstract

The regulation of insulin secretion from RINm5F cells exposed to high voltage discharge has been investigated. Electron microscopy revealed that the overall structure of the cells was preserved after permeabilization. In this preparation insulin release was stimulated by Ca2+ (EC50=2.4 μM). The stable GTP analogue GTPγS enhanced secretion both at intermediate (nano- to micromolar) and vanishingly low (<10 pM) Ca2+ concentrations. At optimal Ca2+ (10 μM) the effect of GTPγS was greatly reduced. We investigated whether the secretory response to GTP analogues was mediated by any of three enzyme systems regulated by GTP-binding proteins, i.e. generation of cyclic AMP by adenylate cyclase, of diacylglycerol by phospholipase C and of arachidonic acid by phospholipase A2. The involvement of these messenger systems could be excluded as (i) cyclic AMP only had minor, Ca2+ dependent effects, (ii) phospholipase C was not activated in the absence of Ca2+ and insulin secretion due to the phorbol ester TPA displayed a different Ca2+ dependency, (iii) arachidonic acid did not elicit Ca2+ independent insulin secretion. These results, taken together with the finding that insulin secretion due to Ca2+ or TPA is attenuated by the inhibitory guanine nucleotide GDPβS, suggest the existence of a regulatory site in exocytosis which is sensitive to guanine nucleotides.

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Abbreviations

InsP3 :

inositol trisphosphate

Ptd-InsP2 :

phosphatidylinositol 4,5-bisphosphate

GTPγS:

guanosine 5′-(3-O-thio)triphosphate

GDPβS:

guanosine 5′-(2-O-thio)diphosphate

Gpp(NH)p:

guanyl-5′-yl imidodiphosphate

TPA:

12-O-tetradecanoylphorbol-13-acetate

OAG:

1-oleoyl-2-acetylglycerol

Hepes:

4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid

EGTA:

(ethylenebis(oxyethylenenitrilo)tetraacetic acid

DAG:

diacylglycerol

[Ca2+]i :

cytosolic free Ca2+ concentration

References

  1. Prentki, M. and Wollheim, C. B. (1984).Experientia 40:1052–1060.

    Google Scholar 

  2. Wollheim, C. B. and Biden, T. J. (1986).J. Biol. Chem. 261:8314–8319.

    Google Scholar 

  3. Berridge, M. J. and Irvine, R. F. (1984).Nature 312:315–321.

    Google Scholar 

  4. Wollheim, C. B. and Biden, T. J. (1986).Ann. N.Y. Acad. Sci. 488:317–333.

    Google Scholar 

  5. Arkhammar, P., Nilsson, T., Rorsman, P. and Berggren, P.-O. (1987).J. Biol. Chem. 262:5448–5454.

    Google Scholar 

  6. Dunlop, M. E. and Larkins, R. G. (1985).Biochem. Biophys. Res. Commun. 132:467–473.

    Google Scholar 

  7. Zawalich, W., Brown, C. and Rasmussen, H. (1983).Biochem. Biophys. Res. Commun. 117: 448–455.

    Google Scholar 

  8. Malaisse, W. J. and Malaisse-Lagae, F. (1984).Experientia 40:1068–1075.

    Google Scholar 

  9. Neher, E. and Marty, A. (1982).Proc. Natl. Acad. Sci. USA 79:6712–6716.

    Google Scholar 

  10. Fernandez, J. M., Neher, E. and Gomperts, B. D. (1984).Nature 312:453–455.

    Google Scholar 

  11. Breckenridge, L. J. and Almers, W. (1987).Proc. Natl. Acad. Sci. USA 84:1945–1949.

    Google Scholar 

  12. Neher, E. (1987).J. Physiol. (Lond.) in press.

  13. Baker, P. F. and Knight, D. E. (1978).Nature 276:620–622.

    Google Scholar 

  14. Haslam, R. J. and Davidson, M. M. L. (1984).FEBS Lett. 174:90–95.

    Google Scholar 

  15. Knight, D. E. and Koh, E. (1984).Cell Calcium 5:401–418.

    Google Scholar 

  16. Ronning, S. A. and Martin, T. F. J. (1986).J. Biol. Chem. 261:7834–7839.

    Google Scholar 

  17. Pace, C. S., Tarvin, J. T., Neighbors, A. S., Pirkle, J. A. and Greider, M. H. (1980).Diabetes 29:911–918.

    Google Scholar 

  18. Yaseen, M. A., Pedley, K. C. and Howell, S. L. (1982).Biochem. J. 206:81–87.

    Google Scholar 

  19. Tamagawa, T., Niki, H. and Niki, A. (1985).FEBS Lett. 183:430–432.

    Google Scholar 

  20. Colca, J. R., Wolf, B. A., Comens, P. G. and McDaniel, M. L. (1985).Biochem. J. 228:529–536.

    Google Scholar 

  21. Best, L. (1986).Biochem. J. 238:773–779.

    Google Scholar 

  22. Gomperts, B. D. (1983).Nature 306:64–66.

    Google Scholar 

  23. Haslam, R. J. and Davidson, M. M. L. (1984).J. Recept. Res. 4:605–629.

    Google Scholar 

  24. Barrowman, M. M., Cockcroft, S. and Gomperts, B. D. (1986).Nature 319:504–507.

    Google Scholar 

  25. Bittner, M. A., Holz, R. W. and Neubig, R. R. (1986).J. Biol. Chem. 261:10182–10188.

    Google Scholar 

  26. Vallar, L., Biden, T. J. and Wollheim, C. B. (1987).J. Biol. Chem. 262:5049–5056.

    Google Scholar 

  27. Cockcroft, S. and Gomperts, B. D. (1985).Nature 314:534–536.

    Google Scholar 

  28. Litosch, I., Wallis, C. and Fain, J. N. (1985).J. Biol. Chem. 260:5464–5471.

    Google Scholar 

  29. Cockcroft, S. (1987).Trends in Biochem. Sci. 12:75–78.

    Google Scholar 

  30. Dunlop, M. E. and Larkins, R. G. (1986).Biochem. J. 240:731–737.

    Google Scholar 

  31. Knight, D. E. and Baker, P. F. (1985).FEBS Lett. 189:345–349.

    Google Scholar 

  32. Howell, T. W., Cockcroft, S. and Gomperts, B. D. (1987).J. Cell Biol. in press.

  33. Arkhammar, P., Nilsson, T. and Berggren, P.-O. (1986).Biochim. Biophys. Acta 887: 236–241.

    Google Scholar 

  34. Gilman, A. G. (1984).J. Clin. Invest. 73:1–4.

    Google Scholar 

  35. Vandenbark, G. R., Kuhn, L. J. and Niedel, J. E. (1984).J. Clin. Invest. 73:448–457.

    Google Scholar 

  36. Irving, H. R. and Exton, J. H. (1987).J. Biol. Chem. 262:3440–3443.

    Google Scholar 

  37. Metz, S. A., Draznin, B., Sussman, K. E. and Leitner, J. W. (1987).Biochem. Biophys. Res. Commun. 142:251–258.

    Google Scholar 

  38. Burch, R. M., Luini, A. and Axelrod, J. (1986).Proc. Natl. Acad. Sci. USA 83: 7201–7205.

    Google Scholar 

  39. Toutant, M., Aunis, D., Bockaert, J., Homburger, V. and Rouot, B. (1987).FEBS Lett. 215:339–344.

    Google Scholar 

  40. Knight, D. E., Tonge, D. A. and Baker, P. F. (1985).Nature 317:719–721.

    Google Scholar 

  41. Knight, D. E. (1986).FEBS Lett. 207:222–226.

    Google Scholar 

  42. Ohashi, Y. and Narumiya, S. (1978).J. Biol. Chem. 262:1430–1433.

    Google Scholar 

  43. Matsuoka, I., Syuto, B., Kurihara, K. and Kubo, S. (1987).FEBS Lett. 216:295–299.

    Google Scholar 

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Wollheim, C.B., Ullrich, S., Meda, P. et al. Regulation of exocytosis in electrically permeabilized insulin-secreting cells. Evidence for Ca2+ dependent and independent secretion. Biosci Rep 7, 443–454 (1987). https://doi.org/10.1007/BF01362507

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