Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1979 Mar 1;73(3):287–305. doi: 10.1085/jgp.73.3.287

Fluid transport and the dimensions of cells and interspaces of living Necturus gallbladder

PMCID: PMC2215164  PMID: 438773

Abstract

The volume of the cells and lateral intercellular spaces were measured in living Necturus gallbladder epithelium. Under control conditions, the volume of the lateral spaces was 9% of the cell volume. Replacement of mucosal NaCl by sucrose or tetramethylammonium chloride (TMACl) caused intercellular spaces to collapse. During mucosal NaCl replacement, cell volume decreased to 79% of its control value. When NaCl was reintroduced into the mucosal bath, the intercellular spaces reopened and the cells returned to control volume. The NaCl active transport rate, calculated from the rate of cell volume decrease, was 266 pM/cm2.s, close to the observed rate of transepithelial salt transport. It was calculated from the decrease in cell volume that all of the intracellular NaCl was transported out of the cell during removal of mucosal NaCl. The flux of salt across the apical membrane, calculated from the rate of cell volume increase upon reintroducing mucosal NaCl, was 209 pM/cm2.s, in good agreement with estimates by other methods. The electrical resistance of the tight junctions was estimated to be 83.9% of the total tissue resistance in control conditions, suggesting that the lateral intercellular spaces normally offer only a small resistance to electrolyte movement.

Full Text

The Full Text of this article is available as a PDF (1.0 MB).

Selected References

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

  1. Blom H., Helander H. F. Quantitative electron microscopical studies on in vitro incubated rabbit gallbladder epithelium. J Membr Biol. 1977 Oct 3;37(1):45–61. doi: 10.1007/BF01940923. [DOI] [PubMed] [Google Scholar]
  2. DIAMOND J. M. The reabsorptive function of the gall-bladder. J Physiol. 1962 May;161:442–473. doi: 10.1113/jphysiol.1962.sp006898. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Diamond J. M., Bossert W. H. Standing-gradient osmotic flow. A mechanism for coupling of water and solute transport in epithelia. J Gen Physiol. 1967 Sep;50(8):2061–2083. doi: 10.1085/jgp.50.8.2061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Frederiksen O., Rostgaard J. Absence of dilated lateral intercellular spaces in fluid-transporting frog gallbladder epithelium. Direct microscopy observations. J Cell Biol. 1974 Jun;61(3):830–834. doi: 10.1083/jcb.61.3.830. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kaye G. I., Wheeler H. O., Whitlock R. T., Lane N. Fluid transport in the rabbit gallbladder. A combined physiological and electron microscopic study. J Cell Biol. 1966 Aug;30(2):237–268. doi: 10.1083/jcb.30.2.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Reuss L., Finn A. L. Electrical properties of the cellular transepithelial pathway in Necturus gallbladder. I. Circuit analysis and steady-state effects of mucosal solution ionic substitutions. J Membr Biol. 1975 Dec 4;25(1-2):115–139. doi: 10.1007/BF01868571. [DOI] [PubMed] [Google Scholar]
  7. Reuss L., Finn A. L. Electrical properties of the cellular transepithelial pathway in Necturus gallbladder. II. Ionic permeability of the apical cell membrane. J Membr Biol. 1975 Dec 4;25(1-2):141–161. doi: 10.1007/BF01868572. [DOI] [PubMed] [Google Scholar]
  8. Spring K. R., Giebisch G. Kinetics of Na+ transport in Necturus proximal tubule. J Gen Physiol. 1977 Sep;70(3):307–328. doi: 10.1085/jgp.70.3.307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Spring K. R., Hope A. Size and shape of the lateral intercellular spaces in a living epithelium. Science. 1978 Apr 7;200(4337):54–58. doi: 10.1126/science.635571. [DOI] [PubMed] [Google Scholar]
  10. Spring K. R., Kimura G. Chloride reabsorption by renal proximal tubules of Necturus. J Membr Biol. 1978 Jan 18;38(3):233–254. doi: 10.1007/BF01871924. [DOI] [PubMed] [Google Scholar]
  11. Tormey J. M., Diamond J. M. The ultrastructural route of fluid transport in rabbit gall bladder. J Gen Physiol. 1967 Sep;50(8):2031–2060. doi: 10.1085/jgp.50.8.2031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. USSING H. H., WINDHAGER E. E. NATURE OF SHUNT PATH AND ACTIVE SODIUM TRANSPORT PATH THROUGH FROG SKIN EPITHELIUM. Acta Physiol Scand. 1964 Aug;61:484–504. [PubMed] [Google Scholar]
  13. Voûte C. L., Ussing H. H. Some morphological aspects of active sodium transport. The epithelium of the frog skin. J Cell Biol. 1968 Mar;36(3):625–638. doi: 10.1083/jcb.36.3.625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. WHITLOCK R. T., WHEELER H. O. COUPLED TRANSPORT OF SOLUTE AND WATER ACROSS RABBIT GALLBLADDER EPITHELIUM. J Clin Invest. 1964 Dec;43:2249–2265. doi: 10.1172/JCI105099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. van Os C. H., Slegers J. F. The electrical potential profile of gallbladder epithelium. J Membr Biol. 1975 Dec 4;24(3-4):341–363. doi: 10.1007/BF01868631. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES