Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1971 Mar 1;48(3):503–522. doi: 10.1083/jcb.48.3.503

CONDENSING VACUOLE CONVERSION AND ZYMOGEN GRANULE DISCHARGE IN PANCREATIC EXOCRINE CELLS: METABOLIC STUDIES

James D Jamieson 1, George E Palade 1
PMCID: PMC2108111  PMID: 5547590

Abstract

We have examined, in the pancreatic exocrine cell, the metabolic requirements for the conversion of condensing vacuoles into zymogen granules and for the discharge of the contents of zymogen granules. To study condensing vacuole conversion, we pulse labeled guinea pig pancreatic slices for 4 min with leucine-3H and incubated them in chase medium for 20 min to allow labeled proteins to reach condensing vacuoles. Glycolytic and respiratory inhibitors were then added and incubation continued for 60 min to enable labeled proteins to reach granules in control slices. Electron microscope radioautography of cells or of zymogen granule pellets from treated slices showed that a large proportion of prelabeled condensing vacuoles underwent conversion in the presence of the combined inhibitors. Osmotic fragility studies on zymogen granule suspensions suggest that condensation may result from the aggregation of secretory proteins in an osmotically inactive form. Discharge was studied using an in vitro radioassay based on the finding that prelabeled zymogen granules can be induced to release their labeled contents to the incubation medium by carbamylcholine or pancreozymin. Induced discharge is not affected if protein synthesis is blocked by cycloheximide for up to 2 hr, but is strictly dependent on respiration. The data indicate that transport and discharge do not require the pari passu synthesis of secretory or nonsecretory proteins (e.g. membrane proteins), suggesting that the cell may reutilize its membranes during the secretory process. The energy requirements for zymogen discharge may be related to the fusion-fission of the granule membrane with the apical plasmalemma.

Full Text

The Full Text of this article is available as a PDF (2.1 MB).

Selected References

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

  1. Amsterdam A., Ohad I., Schramm M. Dynamic changes in the ultrastructure of the acinar cell of the rat parotid gland during the secretory cycle. J Cell Biol. 1969 Jun;41(3):753–773. doi: 10.1083/jcb.41.3.753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Babad H., Ben-Zvi R., Bdolah A., Schramm M. The mechanism of enzyme secretion by the cell. 4. Effects of inducers, substrates and inhibitors on amylase secretion by rat parotid slices. Eur J Biochem. 1967 Mar;1(1):96–101. doi: 10.1111/j.1432-1033.1967.tb00049.x. [DOI] [PubMed] [Google Scholar]
  3. Baudhuin P., Beaufay H., De Duve C. Combined biochemical and morphological study of particulate fractions from rat liver. Analysis of preparations enriched in lysosomes or in particles containing urate oxidase, D-amino acid oxidase, and catalase. J Cell Biol. 1965 Jul;26(1):219–243. doi: 10.1083/jcb.26.1.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bauduin H., Colin M., Dumont J. E. Energy sources for protein synthesis and enzymatic secretion in rat pancreas in vitro. Biochim Biophys Acta. 1969 Feb 18;174(2):722–733. doi: 10.1016/0005-2787(69)90301-3. [DOI] [PubMed] [Google Scholar]
  5. Berneis K. H., Da Prada M., Pletscher A. Micelle formation between 5-hydroxytryptamine and adenosine triphosphate in platelet storage organelles. Science. 1969 Aug 29;165(3896):913–914. doi: 10.1126/science.165.3896.913. [DOI] [PubMed] [Google Scholar]
  6. Borisy G. G., Taylor E. W. The mechanism of action of colchicine. Binding of colchincine-3H to cellular protein. J Cell Biol. 1967 Aug;34(2):525–533. doi: 10.1083/jcb.34.2.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. CARO L. G., PALADE G. E. PROTEIN SYNTHESIS, STORAGE, AND DISCHARGE IN THE PANCREATIC EXOCRINE CELL. AN AUTORADIOGRAPHIC STUDY. J Cell Biol. 1964 Mar;20:473–495. doi: 10.1083/jcb.20.3.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. CARO L. G., VAN TUBERGEN R. P., KOLB J. A. High-resolution autoradiography. I. Methods. J Cell Biol. 1962 Nov;15:173–188. doi: 10.1083/jcb.15.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GREENE L. J., HIRS C. H., PALADE G. E. On the protein composition of bovine pancreatic zymogen granules. J Biol Chem. 1963 Jun;238:2054–2070. [PubMed] [Google Scholar]
  10. HOKIN L. E. Isolation of the zymogen granules of dog pancreas and a study of their properties. Biochim Biophys Acta. 1955 Nov;18(3):379–388. doi: 10.1016/0006-3002(55)90101-3. [DOI] [PubMed] [Google Scholar]
  11. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. 3. Dissociation of intracellular transport from protein synthesis. J Cell Biol. 1968 Dec;39(3):580–588. doi: 10.1083/jcb.39.3.580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. I. Role of the peripheral elements of the Golgi complex. J Cell Biol. 1967 Aug;34(2):577–596. doi: 10.1083/jcb.34.2.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. II. Transport to condensing vacuoles and zymogen granules. J Cell Biol. 1967 Aug;34(2):597–615. doi: 10.1083/jcb.34.2.597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. IV. Metabolic requirements. J Cell Biol. 1968 Dec;39(3):589–603. doi: 10.1083/jcb.39.3.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Jones A. L., Ruderman N. B., Herrera M. G. Electron microscopic and biochemical study of lipoprotein synthesis in the isolated perfused rat liver. J Lipid Res. 1967 Sep;8(5):429–446. [PubMed] [Google Scholar]
  16. Kulka R. G., Sternlicht E. Enzyme secretion in mouse pancreas mediated by adenosine-3'5'-cyclic phosphate and inhibited by adenosine-3'-phosphate. Proc Natl Acad Sci U S A. 1968 Nov;61(3):1123–1128. doi: 10.1073/pnas.61.3.1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lacy P. E., Howell S. L., Young D. A., Fink C. J. New hypothesis of insulin secretion. Nature. 1968 Sep 14;219(5159):1177–1179. doi: 10.1038/2191177a0. [DOI] [PubMed] [Google Scholar]
  18. Lenfant C., Johansen K., Hanson D. Bimodal gas exchange and ventilation-perfusion relationship in lower vertebrates. Fed Proc. 1970 May-Jun;29(3):1124–1129. [PubMed] [Google Scholar]
  19. NOVIKOFF A. B. Cytochemical staining methods for enzyme activities: their application to the rat parotid gland. Jew Mem Hosp Bull. 1962 Mar;6-7:70–93. [PubMed] [Google Scholar]
  20. Olmsted J. B., Carlson K., Klebe R., Ruddle F., Rosenbaum J. Isolation of microtubule protein from cultured mouse neuroblastoma cells. Proc Natl Acad Sci U S A. 1970 Jan;65(1):129–136. doi: 10.1073/pnas.65.1.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Omura T., Siekevitz P., Palade G. E. Turnover of constituents of the endoplasmic reticulum membranes of rat hepatocytes. J Biol Chem. 1967 May 25;242(10):2389–2396. [PubMed] [Google Scholar]
  22. PALADE G. E. Intracisternal granules in the exocrine cells of the pancreas. J Biophys Biochem Cytol. 1956 Jul 25;2(4):417–422. doi: 10.1083/jcb.2.4.417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. PETERS T., Jr The biosynthesis of rat serum albumin. II. Intracellular phenomena in the secretion of newly formed albumin. J Biol Chem. 1962 Apr;237:1186–1189. [PubMed] [Google Scholar]
  24. REDMAN C. M., HOKIN L. E. Phospholipide turnover in microsomal membranes of the pancreas during enzyme secretion. J Biophys Biochem Cytol. 1959 Oct;6:207–214. doi: 10.1083/jcb.6.2.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Ray P. M., Shininger T. L., Ray M. M. ISOLATION OF beta-GLUCAN SYNTHETASE PARTICLES FROM PLANT CELLS AND IDENTIFICATION WITH GOLGI MEMBRANES. Proc Natl Acad Sci U S A. 1969 Oct;64(2):605–612. doi: 10.1073/pnas.64.2.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Redman C. M., Sabatini D. D. Vectorial discharge of peptides released by puromycin from attached ribosomes. Proc Natl Acad Sci U S A. 1966 Aug;56(2):608–615. doi: 10.1073/pnas.56.2.608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Redman C. M., Siekevitz P., Palade G. E. Synthesis and transfer of amylase in pigeon pancreatic micromosomes. J Biol Chem. 1966 Mar 10;241(5):1150–1158. [PubMed] [Google Scholar]
  28. Ridderstap A. S., Bonting S. L. Enzyme secretion by the isolated rabbit pancreas: absence of a relation with the Na-K activated ATPase. Studies on Na-K activated ATPase, XXVII. Pflugers Arch. 1969;313(1):53–61. doi: 10.1007/BF00586328. [DOI] [PubMed] [Google Scholar]
  29. Robison G. A., Butcher R. W., Sutherland E. W. Cyclic AMP. Annu Rev Biochem. 1968;37:149–174. doi: 10.1146/annurev.bi.37.070168.001053. [DOI] [PubMed] [Google Scholar]
  30. SCHRAMM M., DANON D. The mechanism of enzyme secretion by the cell. I. Storage of amylase in the zymogen granules of the rat-parotis gland. Biochim Biophys Acta. 1961 Jun 10;50:102–112. doi: 10.1016/0006-3002(61)91065-4. [DOI] [PubMed] [Google Scholar]
  31. SIEKEVITZ P., PALADE G. E. A cytochemical study on the pancreas of the guinea pig. I. Isolation and enzymatic activities of cell fractions. J Biophys Biochem Cytol. 1958 Mar 25;4(2):203–218. doi: 10.1083/jcb.4.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. SLEIN M. W., CORI G. T., CORI C. F. A comparative study of hexokinase from yeast and animal tissues. J Biol Chem. 1950 Oct;186(2):763–780. [PubMed] [Google Scholar]
  33. Sachs H. Neurosecretion. Adv Enzymol Relat Areas Mol Biol. 1969;32:327–372. doi: 10.1002/9780470122778.ch8. [DOI] [PubMed] [Google Scholar]
  34. Smith R. E., Farquhar M. G. Modulation in nucleoside diphosphatase activity of mammotrophic cells of the rat adenohypophysis during secretion. J Histochem Cytochem. 1970 Apr;18(4):237–250. doi: 10.1177/18.4.237. [DOI] [PubMed] [Google Scholar]
  35. de Potter W. P., de Schaepdryver A. F., Moerman E. J., Smith A. D. Evidence for the release of vesicle-proteins together with noradrenaline upon stimulation of the splenic nerve. J Physiol. 1969 Oct;204(2):102P+–102P+. [PubMed] [Google Scholar]

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

RESOURCES