Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1987 Jul 1;105(1):145–153. doi: 10.1083/jcb.105.1.145

Newly synthesized proinsulin/insulin and stored insulin are released from pancreatic B cells predominantly via a regulated, rather than a constitutive, pathway

PMCID: PMC2114904  PMID: 3301864

Abstract

The pancreatic B cell has been used as a model to compare the release of newly synthesized prohormone/hormone with that of stored hormone. Secretion of newly synthesized proinsulin/insulin (labeled with [3H]leucine during a 5-min pulse) and stored total immunoreactive insulin was monitored from isolated rat pancreatic islets at basal and stimulatory glucose concentrations over 180 min. By 180 min, 15% of the islet content of stored insulin was released at 16.7 mM glucose compared with 2% at 2.8 mM glucose. After a 30-min lag period, release of newly synthesized (labeled) proinsulin and insulin was detected; from 60 min onwards this release was stimulated up to 11-fold by 16.7 mM glucose. At 180 min, 60% of the initial islet content of labeled proinsulin was released at 16.7 mM glucose and 6% at 2.8 mM glucose. Specific radioactivity of the released newly synthesized hormone relative to that of material in islets indicated its preferential release. A similar degree of isotopic enrichment of released, labeled products was observed at both glucose concentrations. Quantitative HPLC analysis of labeled products indicated that glucose had no effect on intracellular proinsulin to insulin conversion; release of both newly synthesized proinsulin and insulin was sensitive to glucose stimulation; 90% of the newly synthesized hormone was released as insulin; and only 0.5% of proinsulin was rapidly released (between 30 and 60 min) in a glucose-independent fashion. It is thus concluded that the major portion of released hormone, whether old or new, processed or unprocessed, is directed through the regulated pathway, and therefore the small (less than 1%) amount released via a constitutive pathway cannot explain the preferential release of newly formed products from the B cell.

Full Text

The Full Text of this article is available as a PDF (904.4 KB).

Selected References

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

  1. Allan V. J., Kreis T. E. A microtubule-binding protein associated with membranes of the Golgi apparatus. J Cell Biol. 1986 Dec;103(6 Pt 1):2229–2239. doi: 10.1083/jcb.103.6.2229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Berne C. Anti-insulin serum coupled to Sepharose 4B as a tool for the investigation of insulin biosynthesis in the B-cells of obese hyperglycemic mice. Endocrinology. 1975 Nov;97(5):1241–1247. doi: 10.1210/endo-97-5-1241. [DOI] [PubMed] [Google Scholar]
  3. Elks M. L., Youngblood W. W., Kizer J. S. Serotonin synthesis and release in brain slices: independence of tryptophan. Brain Res. 1979 Aug 31;172(3):471–486. doi: 10.1016/0006-8993(79)90580-8. [DOI] [PubMed] [Google Scholar]
  4. Galski H., Weinstein D., Abraham K., de Groot N., Segal S., Folman R., Hochberg A. A. The in vitro synthesis and secretion of alkaline phosphatase from first trimester human decidua. Eur J Obstet Gynecol Reprod Biol. 1982 Oct;14(1):1–11. doi: 10.1016/0028-2243(82)90079-x. [DOI] [PubMed] [Google Scholar]
  5. Gold G., Gishizky M. L., Chick W. L., Grodsky G. M. Contrasting patterns of insulin biosynthesis, compartmental storage, and secretion. Rat tumor versus islet cells. Diabetes. 1984 Jun;33(6):556–561. doi: 10.2337/diab.33.6.556. [DOI] [PubMed] [Google Scholar]
  6. Gold G., Gishizky M. L., Grodsky G. M. Evidence that glucose "marks" beta cells resulting in preferential release of newly synthesized insulin. Science. 1982 Oct 1;218(4567):56–58. doi: 10.1126/science.6181562. [DOI] [PubMed] [Google Scholar]
  7. Gold G., Pou J., Gishizky M. L., Landahl H. D., Grodsky G. M. Effects of tolbutamide pretreatment on the rate of conversion of newly synthesized proinsulin to insulin and the compartmental characteristics of insulin storage in isolated rat islets. Diabetes. 1986 Jan;35(1):6–12. doi: 10.2337/diab.35.1.6. [DOI] [PubMed] [Google Scholar]
  8. Green R., Shields D. Somatostatin discriminates between the intracellular pathways of secretory and membrane proteins. J Cell Biol. 1984 Jul;99(1 Pt 1):97–104. doi: 10.1083/jcb.99.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gumbiner B., Kelly R. B. Two distinct intracellular pathways transport secretory and membrane glycoproteins to the surface of pituitary tumor cells. Cell. 1982 Jan;28(1):51–59. doi: 10.1016/0092-8674(82)90374-9. [DOI] [PubMed] [Google Scholar]
  10. Halban P. A., Amherdt M., Orci L., Renold A. E. Tris(hydroxymethyl)aminomethane inhibits the synthesis and processing of proinsulin in isolated rat pancreatic islets without affecting release of insulin stores. Diabetes. 1986 Apr;35(4):433–439. doi: 10.2337/diab.35.4.433. [DOI] [PubMed] [Google Scholar]
  11. Halban P. A. Differential rates of release of newly synthesized and of stored insulin from pancreatic islets. Endocrinology. 1982 Apr;110(4):1183–1188. doi: 10.1210/endo-110-4-1183. [DOI] [PubMed] [Google Scholar]
  12. Halban P. A. Inhibition of proinsulin to insulin conversion in rat islets using arginine and lysine analogs. Lack of effect on rate of release of modified products. J Biol Chem. 1982 Nov 25;257(22):13177–13180. [PubMed] [Google Scholar]
  13. Halban P. A., Renold A. E. Influence of glucose on insulin handling by rat islets in culture. A reflection of integrated changes in insulin biosynthesis, release, and intracellular degradation. Diabetes. 1983 Mar;32(3):254–261. doi: 10.2337/diab.32.3.254. [DOI] [PubMed] [Google Scholar]
  14. Halban P. A., Rhodes C. J., Shoelson S. E. High-performance liquid chromatography (HPLC): a rapid, flexible and sensitive method for separating islet proinsulin and insulin. Diabetologia. 1986 Dec;29(12):893–896. doi: 10.1007/BF00870146. [DOI] [PubMed] [Google Scholar]
  15. Halban P. A., Wollheim C. B., Blondel B., Renold A. E. Long-term exposure of isolated pancreatic islets to mannoheptulose: evidence for insulin degradation in the beta cell. Biochem Pharmacol. 1980 Oct 1;29(19):2625–2633. doi: 10.1016/0006-2952(80)90077-5. [DOI] [PubMed] [Google Scholar]
  16. Halban P. A., Wollheim C. B. Intracellular degradation of insulin stores by rat pancreatic islets in vitro. An alternative pathway for homeostasis of pancreatic insulin content. J Biol Chem. 1980 Jul 10;255(13):6003–6006. [PubMed] [Google Scholar]
  17. Hedeskov C. J. Mechanism of glucose-induced insulin secretion. Physiol Rev. 1980 Apr;60(2):442–509. doi: 10.1152/physrev.1980.60.2.442. [DOI] [PubMed] [Google Scholar]
  18. Herbert V., Lau K. S., Gottlieb C. W., Bleicher S. J. Coated charcoal immunoassay of insulin. J Clin Endocrinol Metab. 1965 Oct;25(10):1375–1384. doi: 10.1210/jcem-25-10-1375. [DOI] [PubMed] [Google Scholar]
  19. Hoff J. D., Lasley B. L., Wang C. F., Yen S. S. The two pools of pituitary gonadotropin: regulation during the menstrual cycle. J Clin Endocrinol Metab. 1977 Feb;44(2):302–312. doi: 10.1210/jcem-44-2-302. [DOI] [PubMed] [Google Scholar]
  20. Howell S. L., Taylor K. W. The secretion of newly synthesized insulin in vitro. Biochem J. 1967 Mar;102(3):922–927. doi: 10.1042/bj1020922. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Howell S. L. The mechanism of insulin secretion. Diabetologia. 1984 May;26(5):319–327. doi: 10.1007/BF00266030. [DOI] [PubMed] [Google Scholar]
  22. Hutton J. C. Secretory granules. Experientia. 1984 Oct 15;40(10):1091–1098. doi: 10.1007/BF01971456. [DOI] [PubMed] [Google Scholar]
  23. Kelly R. B. Pathways of protein secretion in eukaryotes. Science. 1985 Oct 4;230(4721):25–32. doi: 10.1126/science.2994224. [DOI] [PubMed] [Google Scholar]
  24. Lucocq J., Montesano R. Nonrandom positioning of Golgi apparatus in pancreatic B cells. Anat Rec. 1985 Oct;213(2):182–186. doi: 10.1002/ar.1092130210. [DOI] [PubMed] [Google Scholar]
  25. MacGregor R. R., Hamilton J. W., Cohn D. V. The by-pass of tissue hormone stores during the secretion of newly synthesized parathyroid hormone. Endocrinology. 1975 Jul;97(1):178–188. doi: 10.1210/endo-97-1-178. [DOI] [PubMed] [Google Scholar]
  26. Moore H. P., Gumbiner B., Kelly R. B. Chloroquine diverts ACTH from a regulated to a constitutive secretory pathway in AtT-20 cells. 1983 Mar 31-Apr 6Nature. 302(5907):434–436. doi: 10.1038/302434a0. [DOI] [PubMed] [Google Scholar]
  27. Moore H. P., Walker M. D., Lee F., Kelly R. B. Expressing a human proinsulin cDNA in a mouse ACTH-secreting cell. Intracellular storage, proteolytic processing, and secretion on stimulation. Cell. 1983 Dec;35(2 Pt 1):531–538. doi: 10.1016/0092-8674(83)90187-3. [DOI] [PubMed] [Google Scholar]
  28. Nagamatsu S., Bolaffi J. L., Grodsky G. M. Direct effects of glucose on proinsulin synthesis and processing during desensitization. Endocrinology. 1987 Apr;120(4):1225–1231. doi: 10.1210/endo-120-4-1225. [DOI] [PubMed] [Google Scholar]
  29. Noel J., Rabinovitch A., Olson L., Kyriakides G., Miller J., Mintz D. H. A method for large-scale, high-yield isolation of canine pancreatic islets of Langerhans. Metabolism. 1982 Feb;31(2):184–187. doi: 10.1016/0026-0495(82)90133-0. [DOI] [PubMed] [Google Scholar]
  30. Orci L., Ravazzola M., Amherdt M., Madsen O., Vassalli J. D., Perrelet A. Direct identification of prohormone conversion site in insulin-secreting cells. Cell. 1985 Sep;42(2):671–681. doi: 10.1016/0092-8674(85)90124-2. [DOI] [PubMed] [Google Scholar]
  31. Orci L. The insulin factory: a tour of the plant surroundings and a visit to the assembly line. The Minkowski lecture 1973 revisited. Diabetologia. 1985 Aug;28(8):528–546. doi: 10.1007/BF00281987. [DOI] [PubMed] [Google Scholar]
  32. Palade G. Intracellular aspects of the process of protein synthesis. Science. 1975 Aug 1;189(4200):347–358. doi: 10.1126/science.1096303. [DOI] [PubMed] [Google Scholar]
  33. Piercy M., Shin S. H. Newly synthesized prolactin is preferentially secreted by the adenohypophysis in a primary cell culture system. Mol Cell Endocrinol. 1981 Jan;21(1):75–84. doi: 10.1016/0303-7207(81)90032-0. [DOI] [PubMed] [Google Scholar]
  34. Sachs H., Fawcett P., Takabatake Y., Portanova R. Biosynthesis and release of vasopressin and neurophysin. Recent Prog Horm Res. 1969;25:447–491. doi: 10.1016/b978-0-12-571125-8.50013-2. [DOI] [PubMed] [Google Scholar]
  35. 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]
  36. Sando H., Borg J., Steiner D. F. Studies on the secretion of newly synthesized proinsulin and insulin from isolated rat islets of Langerhans. J Clin Invest. 1972 Jun;51(6):1476–1485. doi: 10.1172/JCI106944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Slaby F., Bryan J. High uptake of myo-inositol by rat pancreatic tissue in vitro stimulates secretion. J Biol Chem. 1976 Aug 25;251(16):5078–5086. [PubMed] [Google Scholar]
  38. Stachura M. E. Basal and dibutyryl cyclic AMP-stimulated release of newly synthesized and stored growth hormone from perifused rat pituitaries. Endocrinology. 1976 Mar;98(3):580–589. doi: 10.1210/endo-98-3-580. [DOI] [PubMed] [Google Scholar]
  39. Stachura M. E., Frohman L. A. Growth hormone: independent release of big and small forms from rat pituitary in vitro. Science. 1975 Feb 7;187(4175):447–449. doi: 10.1126/science.1111113. [DOI] [PubMed] [Google Scholar]
  40. Suwa S., Friesen H. Biosynthesis of human placental proteins and human placental lactogen (HPL) in vitro. II. Dynamic studies of normal term placentas. Endocrinology. 1969 Dec;85(6):1037–1045. doi: 10.1210/endo-85-6-1037. [DOI] [PubMed] [Google Scholar]
  41. Swearingen K. C. Heterogeneous turnover of adenohypophysial prolactin. Endocrinology. 1971 Dec;89(6):1380–1388. doi: 10.1210/endo-89-6-1380. [DOI] [PubMed] [Google Scholar]
  42. Walker A. M., Farquhar M. G. Preferential release of newly synthesized prolactin granules is the result of functional heterogeneity among mammotrophs. Endocrinology. 1980 Oct;107(4):1095–1104. doi: 10.1210/endo-107-4-1095. [DOI] [PubMed] [Google Scholar]
  43. Weiler M. H., Gundersen C. B., Jenden D. J. Choline uptake and acetylcholine synthesis in synaptosomes: investigations using two different labeled variants of choline. J Neurochem. 1981 May;36(5):1802–1812. doi: 10.1111/j.1471-4159.1981.tb00434.x. [DOI] [PubMed] [Google Scholar]
  44. Weinstein D., Galski H., Schenker J. G., Lorberboum H., de Groot N., Ilan J., Folman R., Hochberg A. A. The synthesis and secretion of human placental lactogen (hPL) in cultured term placenta. Mol Cell Endocrinol. 1982 Apr;26(1-2):189–199. doi: 10.1016/0303-7207(82)90016-8. [DOI] [PubMed] [Google Scholar]

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

RESOURCES