Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1980 Dec 1;87(3):736–745. doi: 10.1083/jcb.87.3.736

Experimental modulation of occluding junctions in a cultured transporting epithelium

PMCID: PMC2110771  PMID: 6780571

Abstract

The experimental opening and resealing of occluding junctions in monolayers of cultured MDCK cells (epithelioid of renal origin) was explored by measuring changes in the electrical resistance across the monolayer and by freeze-fracture electron microscopy. As in natural epithelia, the function of occluding junctions as permeability barriers specifically depends on extracellular Ca++ concentration and fails if this ion is replaced by Mg++ or Ba++. The removal of Ca++ and the addition of EGTA to the bathing medium opened the junctions and reduced the transepithelial resistance. Resealing was achieved within 10-15 min by restoring Ca++. Quantitative freeze-fracture electron microscopy showed that junctional opening, caused by lack of Ca++, was accompanied by simplification of the pattern of the membrane strands of the occluding junction without disassembly or displacement of the junctional components. Resealing of the cellular contacts involved the gradual return to a normal junctional pattern estimated as the average number of strands constituting the junction. The occluding junctions were also opened by the addition of the ionophore A23187, suggesting that the sealing of the contacts requires high Ca++ on the extracellular side and low Ca++ concentration of the cytoplasmic compartment. The opening process could be blocked by low temperature (7.5 degrees C). Resealing did not depend on serum factors and did not require protein synthesis; therefore, it seems to be caused by reassembly of preexisting membrane junctional components. The restoration of the junctions occurred simultaneously with the establishment of ion-selective channels; the Na+/Cl- and the cation/cation selectivity were recovered with the same time-course as the electrical resistance. The role of the cytoskeleton in the process of junctional reassembly is reported in the companion article.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

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

  1. Amsterdam A., Jamieson J. D. Studies on dispersed pancreatic exocrine cells. I. Dissociation technique and morphologic characteristics of separated cells. J Cell Biol. 1974 Dec;63(3):1037–1056. doi: 10.1083/jcb.63.3.1037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arias I. M., Doyle D., Schimke R. T. Studies on the synthesis and degradation of proteins of the endoplasmic reticulum of rat liver. J Biol Chem. 1969 Jun 25;244(12):3303–3315. [PubMed] [Google Scholar]
  3. CURRAN P. F., GILL J. R., Jr The effect of calcium on sodium transport by frog skin. J Gen Physiol. 1962 Mar;45:625–641. doi: 10.1085/jgp.45.4.625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cereijido M., Stefani E., Palomo A. M. Occluding junctions in a cultured transporting epithelium: structural and functional heterogeneity. J Membr Biol. 1980 Mar 31;53(1):19–32. doi: 10.1007/BF01871169. [DOI] [PubMed] [Google Scholar]
  5. FORTE J. G., NAUSS A. H. EFFECTS OF CALCIUM REMOVAL ON BULLFROG GASTRIC MUCOSA. Am J Physiol. 1963 Oct;205:631–637. doi: 10.1152/ajplegacy.1963.205.4.631. [DOI] [PubMed] [Google Scholar]
  6. Friend D. S., Gilula N. B. Variations in tight and gap junctions in mammalian tissues. J Cell Biol. 1972 Jun;53(3):758–776. doi: 10.1083/jcb.53.3.758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. 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]
  8. Johnson R., Hammer M., Sheridan J., Revel J. P. Gap junction formation between reaggregated Novikoff hepatoma cells. Proc Natl Acad Sci U S A. 1974 Nov;71(11):4536–4540. doi: 10.1073/pnas.71.11.4536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Leighton J., Brada Z., Estes L. W., Justh G. Secretory activity and oncogenicity of a cell line (MDCK) derived from canine kidney. Science. 1969 Jan 31;163(3866):472–473. doi: 10.1126/science.163.3866.472. [DOI] [PubMed] [Google Scholar]
  10. Loewenstein W. R. Cell surface membranes in close contact. Role of calcium and magnesium ions. J Colloid Interface Sci. 1967 Sep;25(1):34–46. doi: 10.1016/0021-9797(67)90007-0. [DOI] [PubMed] [Google Scholar]
  11. Marin M. L., Gordon R. E., Lane B. P. Development of tight junctions in rat tracheal epithelium during the early hours after mechanical injury. Am Rev Respir Dis. 1979 Jan;119(1):101–106. doi: 10.1164/arrd.1979.119.1.101. [DOI] [PubMed] [Google Scholar]
  12. Martínez-Palomo A., Erlij D. Structure of tight junctions in epithelia with different permeability. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4487–4491. doi: 10.1073/pnas.72.11.4487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Meldolesi J., Castiglioni G., Parma R., Nassivera N., De Camilli P. Ca++-dependent disassembly and reassembly of occluding junctions in guinea pig pancreatic acinar cells. Effect of drugs. J Cell Biol. 1978 Oct;79(1):156–172. doi: 10.1083/jcb.79.1.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Metz J., Forssman W. G., Ito S. Exocrine pancreas under experimental conditions. III. Membrane and cell junctions in isolated acinar cells. Cell Tissue Res. 1977 Feb 14;177(4):459–474. doi: 10.1007/BF00220607. [DOI] [PubMed] [Google Scholar]
  15. Meza I., Ibarra G., Sabanero M., Martínez-Palomo A., Cereijido M. Occluding junctions and cytoskeletal components in a cultured transporting epithelium. J Cell Biol. 1980 Dec;87(3 Pt 1):746–754. doi: 10.1083/jcb.87.3.746. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Misfeldt D. S., Hamamoto S. T., Pitelka D. R. Transepithelial transport in cell culture. Proc Natl Acad Sci U S A. 1976 Apr;73(4):1212–1216. doi: 10.1073/pnas.73.4.1212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Montesano R., Friend D. S., Perrelet A., Orci L. In vivo assembly of tight junctions in fetal rat liver. J Cell Biol. 1975 Nov;67(2PT1):310–319. doi: 10.1083/jcb.67.2.310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Nicolson G. L. Transmembrane control of the receptors on normal and tumor cells. I. Cytoplasmic influence over surface components. Biochim Biophys Acta. 1976 Apr 13;457(1):57–108. doi: 10.1016/0304-4157(76)90014-9. [DOI] [PubMed] [Google Scholar]
  19. Orci L., Amherdt M., Henquin J. C., Lambert A. E., Unger R. H., Renold A. E. Pronase effect on pancreatic beta cell secretion and morphology. Science. 1973 May 11;180(4086):647–649. doi: 10.1126/science.180.4086.647. [DOI] [PubMed] [Google Scholar]
  20. Porvaznik M., Johnson R. G., Sheridan J. D. Tight junction development between cultured hepatoma cells: possible stages in assembly and enhancement with dexamethasone. J Supramol Struct. 1979;10(1):13–30. doi: 10.1002/jss.400100103. [DOI] [PubMed] [Google Scholar]
  21. Rabito C. A., Tchao R., Valentich J., Leighton J. Distribution and characteristics of the occluding junctions in a monolayer of a cell line (MDCK) derived from canine kidney. J Membr Biol. 1978 Nov 8;43(4):351–365. doi: 10.1007/BF01871696. [DOI] [PubMed] [Google Scholar]
  22. Rose B., Loewenstein W. R. Permeability of a cell junction and the local cytoplasmic free ionized calcium concentration: a study with aequorin. J Membr Biol. 1976 Aug 27;28(1):87–119. doi: 10.1007/BF01869692. [DOI] [PubMed] [Google Scholar]
  23. Rose B., Loewenstein W. R. Permeability of cell junction depends on local cytoplasmic calcium activity. Nature. 1975 Mar 20;254(5497):250–252. doi: 10.1038/254250a0. [DOI] [PubMed] [Google Scholar]
  24. SEDAR A. W., FORTE J. G. EFFECTS OF CALCIUM DEPLETION ON THE JUNCTIONAL COMPLEX BETWEEN OXYNTIC CELLS OF GASTRIC GLANDS. J Cell Biol. 1964 Jul;22:173–188. doi: 10.1083/jcb.22.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Shimono M., Clementi F. Intercellular junctions of oral epithelium. II. Ultrastructural changes in rat buccal epithelium induced by trypsin digestion. J Ultrastruct Res. 1977 Apr;59(1):101–112. doi: 10.1016/s0022-5320(77)80032-4. [DOI] [PubMed] [Google Scholar]
  26. Staehelin L. A. Further observations on the fine structure of freeze-cleaved tight junctions. J Cell Sci. 1973 Nov;13(3):763–786. doi: 10.1242/jcs.13.3.763. [DOI] [PubMed] [Google Scholar]
  27. Weihing R. R. The cytoskeleton and plasma membrane. Methods Achiev Exp Pathol. 1979;8:42–109. [PubMed] [Google Scholar]
  28. Wiedner G., Wright E. M. The role of the lateral intercellular spaces in the control of ion permeation across the rabbit gall bladder. Pflugers Arch. 1975 Jul 9;358(1):27–40. doi: 10.1007/BF00584567. [DOI] [PubMed] [Google Scholar]

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

RESOURCES