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. 1981 Nov 1;91(2):584–588. doi: 10.1083/jcb.91.2.584

Role of osmotic forces in exocytosis: studies of ADH-induced fusion in toad urinary bladder

PMCID: PMC2111984  PMID: 6796595

Abstract

Antidiuretic hormone (ADH) treatment of toad urinary bladder activates an exocytotic-like process by which intramembrane particle aggregates are transferred from membranes of elongated cytoplasmic tubules to the luminal-facing plasma membrane. We find that the number of these ADH- induced fusion events, and the number of aggregates appearing in the luminal membrane, are reduced when the luminal bathing medium is made hyperosmotic. As an apparent consequence of the inhibition of their fusion with the luminal membrane, the elongated cytoplasmic tubules become enormously swollen into large, rounded vesicles. These results are consistent with the view that osmotic forces are essential to the basic mechanism of exocytosis.

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Selected References

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  1. Brown E. M., Pazoles C. J., Creutz C. E., Aurbach G. D., Pollard H. B. Role of anions in parathyroid hormone release from dispersed bovine parathyroid cells. Proc Natl Acad Sci U S A. 1978 Feb;75(2):876–880. doi: 10.1073/pnas.75.2.876. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chevalier J., Bourguet J., Hugon J. S. Membrane associated particles: distribution in frog urinary bladder epithelium at rest and after oxytocin treatment. Cell Tissue Res. 1974;152(2):129–140. doi: 10.1007/BF00224690. [DOI] [PubMed] [Google Scholar]
  3. Civan M. M., DiBona D. Pathways for movement of ions and water across toad urinary bladder. II. Site and mode of action of vasopressin. J Membr Biol. 1974;19(3):195–220. doi: 10.1007/BF01869978. [DOI] [PubMed] [Google Scholar]
  4. Cohen F. S., Zimmerberg J., Finkelstein A. Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. II. Incorporation of a vesicular membrane marker into the planar membrane. J Gen Physiol. 1980 Mar;75(3):251–270. doi: 10.1085/jgp.75.3.251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DiBona D. R., Civan M. M. Pathways for movement of ions and water across toad urinary bladder. I. Anatomic site of transepithelial shunt pathways. J Membr Biol. 1973;12(2):101–128. doi: 10.1007/BF01869994. [DOI] [PubMed] [Google Scholar]
  6. Dratwa M., Tisher C. C., Sommer J. R., Croker B. P., Jr Intramembranous particle aggregation in toad urinary bladder after vasopressin stimulation. Lab Invest. 1979 Jan;40(1):46–54. [PubMed] [Google Scholar]
  7. Ellis S. J., Kachadorian W. A., DiScala V. A. Effect of osmotic gradient on ADH-induced intramembranous particle aggregates in toad bladder. J Membr Biol. 1980;52(2):181–184. doi: 10.1007/BF01869124. [DOI] [PubMed] [Google Scholar]
  8. Humbert F., Montesano R., Grosso A., de Sousa R. C., Orci L. Particle aggregates in plasma and intracellular membranes of toad bladder (granular cell). Experientia. 1977 Oct 15;33(10):1364–1367. doi: 10.1007/BF01920184. [DOI] [PubMed] [Google Scholar]
  9. Kachadorian W. A., Levine S. D., Wade J. B., Di Scala V. A., Hays R. M. Relationship of aggregated intramembranous particles to water permeability in vasopressin-treated toad urinary bladder. J Clin Invest. 1977 Mar;59(3):576–581. doi: 10.1172/JCI108673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kachadorian W. A., Wade J. B., DiScala V. A. Vasopressin: induced structural change in toad bladder luminal membrane. Science. 1975 Oct 3;190(4209):67–69. doi: 10.1126/science.809840. [DOI] [PubMed] [Google Scholar]
  11. Muller J., Kachadorian W. A., DiScala V. A. Evidence that ADH-stimulated intramembrane particle aggregates are transferred from cytoplasmic to luminal membranes in toad bladder epithelial cells. J Cell Biol. 1980 Apr;85(1):83–95. doi: 10.1083/jcb.85.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. PEACHEY L. D., RASMUSSEN H. Structure of the toad's urinary bladder as related to its physiology. J Biophys Biochem Cytol. 1961 Aug;10:529–553. doi: 10.1083/jcb.10.4.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pazoles C. J., Pollard H. B. Evidence for stimulation of anion transport in ATP-evoked transmitter release from isolated secretory vesicles. J Biol Chem. 1978 Jun 10;253(11):3962–3969. [PubMed] [Google Scholar]
  14. Satir B., Schooley C., Satir P. Membrane fusion in a model system. Mucocyst secretion in Tetrahymena. J Cell Biol. 1973 Jan;56(1):153–176. doi: 10.1083/jcb.56.1.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Spinelli F., Grosso A., de Sousa R. C. The hydrosmotic effect of vasopressin: a scanning electrom-microscope study. J Membr Biol. 1975 Aug 29;23(2):139–156. doi: 10.1007/BF01870248. [DOI] [PubMed] [Google Scholar]
  16. Wade J. B. Membrane structural specialization of the toad urinary bladder revealed by the freeze-fracture technique. III. Location, structure and vasopressin dependence of intramembrane particle arrays. J Membr Biol. 1978;40(Spec No):281–296. doi: 10.1007/BF02026011. [DOI] [PubMed] [Google Scholar]
  17. Wade J. B., Revel J. P., DiScala V. A. Effect of osmotic gradients on intercellular junctions of the toad bladder. Am J Physiol. 1973 Feb;224(2):407–415. doi: 10.1152/ajplegacy.1973.224.2.407. [DOI] [PubMed] [Google Scholar]
  18. Zimmerberg J., Cohen F. S., Finkelstein A. Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. I. Discharge of vesicular contents across the planar membrane. J Gen Physiol. 1980 Mar;75(3):241–250. doi: 10.1085/jgp.75.3.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Zimmerberg J., Cohen F. S., Finkelstein A. Micromolar Ca2+ stimulates fusion of lipid vesicles with planar bilayers containing a calcium-binding protein. Science. 1980 Nov 21;210(4472):906–908. doi: 10.1126/science.7434004. [DOI] [PubMed] [Google Scholar]
  20. Zivin J. A., Bartko J. J. Statistics for disinterested scientists. Life Sci. 1976 Jan 1;18(1):15–26. doi: 10.1016/0024-3205(76)90268-x. [DOI] [PubMed] [Google Scholar]

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