Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1984 Apr 1;98(4):1209–1221. doi: 10.1083/jcb.98.4.1209

Zonulae occludentes in junctional complex-enriched fractions from mouse liver: preliminary morphological and biochemical characterization

PMCID: PMC2113227  PMID: 6425301

Abstract

A bile canaliculus-derived preparation containing junctional complexes has been obtained from mouse livers using subcellular fractionation techniques. The junctional complexes include structurally intact zonulae occludentes (ZOs). Extraction of this preparation with the anionic detergent sodium deoxycholate (DOC) left junctional ribbons, the detergent-insoluble zonular remnants of the junctional complexes. When visualized in negative stain electron microscopy, each of these ribbons contained a branching and anastomosing network of fibrils which appears similar to that of ZOs in freeze-fractured whole liver. Comparative measurements of freeze-fracture and negative stain fibril diameters and network densities support this relationship. SDS polyacrylamide gel analysis shows the DOC-insoluble junctional ribbons to be characterized by major polypeptides at 37,000 and at 48,000, with minor bands at 34,000, 41,000, 71,000, 86,000, 92,000, and 102,000. The ZO-containing membrane fractions have been isolated in the presence of EGTA in concentrations and under conditions shown by others to disrupt normal ZO morphology and physiology in whole living epithelia. The network of fibrils visualized in these fractions by negative staining is structurally resistant to treatment with DOC, but is either solubilized or disrupted by N-lauroylsarcosine.

Full Text

The Full Text of this article is available as a PDF (1.7 MB).

Selected References

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

  1. Begg D. A., Rodewald R., Rebhun L. I. The visualization of actin filament polarity in thin sections. Evidence for the uniform polarity of membrane-associated filaments. J Cell Biol. 1978 Dec;79(3):846–852. doi: 10.1083/jcb.79.3.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benedetti E. L., Emmelot P. Hexagonal array of subunits in tight junctions separated from isolated rat liver plasma membranes. J Cell Biol. 1968 Jul;38(1):15–24. doi: 10.1083/jcb.38.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berry M. N., Friend D. S. High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study. J Cell Biol. 1969 Dec;43(3):506–520. doi: 10.1083/jcb.43.3.506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Branton D. Fracture faces of frozen membranes. Proc Natl Acad Sci U S A. 1966 May;55(5):1048–1056. doi: 10.1073/pnas.55.5.1048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. CURRAN P. F., ZADUNAISKY J., GILL J. R., Jr The effect of ethylenediaminetetraacetate on ion permeability of the isolated frog skin. Biochim Biophys Acta. 1961 Sep 16;52:392–395. doi: 10.1016/0006-3002(61)90694-1. [DOI] [PubMed] [Google Scholar]
  6. Cassidy M. M., Tidball C. S. Cellular mechanism of intestinal permeability alterations produced by chelation depletion. J Cell Biol. 1967 Mar;32(3):685–698. doi: 10.1083/jcb.32.3.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cereijido M., Robbins E. S., Dolan W. J., Rotunno C. A., Sabatini D. D. Polarized monolayers formed by epithelial cells on a permeable and translucent support. J Cell Biol. 1978 Jun;77(3):853–880. doi: 10.1083/jcb.77.3.853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Claude P., Goodenough D. A. Fracture faces of zonulae occludentes from "tight" and "leaky" epithelia. J Cell Biol. 1973 Aug;58(2):390–400. doi: 10.1083/jcb.58.2.390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Drochmans P., Freudenstein C., Wanson J. C., Laurent L., Keenan T. W., Stadler J., Leloup R., Franke W. W. Structure and biochemical composition of desmosomes and tonofilaments isolated from calf muzzle epidermis. J Cell Biol. 1978 Nov;79(2 Pt 1):427–443. doi: 10.1083/jcb.79.2.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dunia I., Sen Ghosh C., Benedetti E. L., Zweers A., Bloemendal H. Isolation and protein pattern of eye lens fiber junctions. FEBS Lett. 1974 Sep 1;45(1):139–144. doi: 10.1016/0014-5793(74)80831-8. [DOI] [PubMed] [Google Scholar]
  11. EMMELOT P., BOS C. J., BENEDETTI E. L., RUEMKE P. STUDIES ON PLASMA MEMBRANES. I. CHEMICAL COMPOSITION AND ENZYME CONTENT OF PLASMA MEMBRANES ISOLATED FROM RAT LIVER. Biochim Biophys Acta. 1964 Jul 15;90:126–145. doi: 10.1016/0304-4165(64)90125-4. [DOI] [PubMed] [Google Scholar]
  12. Easter D. W., Wade J. B., Boyer J. L. Structural integrity of hepatocyte tight junctions. J Cell Biol. 1983 Mar;96(3):745–749. doi: 10.1083/jcb.96.3.745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. FARQUHAR M. G., PALADE G. E. Junctional complexes in various epithelia. J Cell Biol. 1963 May;17:375–412. doi: 10.1083/jcb.17.2.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 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]
  15. Fairbanks G., Steck T. L., Wallach D. F. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 Jun 22;10(13):2606–2617. doi: 10.1021/bi00789a030. [DOI] [PubMed] [Google Scholar]
  16. Franke W. W., Moll R., Schiller D. L., Schmid E., Kartenbeck J., Mueller H. Desmoplakins of epithelial and myocardial desmosomes are immunologically and biochemically related. Differentiation. 1982;23(2):115–127. doi: 10.1111/j.1432-0436.1982.tb01274.x. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. Frömter E., Diamond J. Route of passive ion permeation in epithelia. Nat New Biol. 1972 Jan 5;235(53):9–13. doi: 10.1038/newbio235009a0. [DOI] [PubMed] [Google Scholar]
  19. Frömter E. The route of passive ion movement through the epithelium of Necturus gallbladder. J Membr Biol. 1972;8(3):259–301. doi: 10.1007/BF01868106. [DOI] [PubMed] [Google Scholar]
  20. Galli P., Brenna A., Camilli de P., Meldolesi J. Extracellular calcium and the organization of tight junctions in pancreatic acinar cells. Exp Cell Res. 1976 Apr;99(1):178–183. doi: 10.1016/0014-4827(76)90694-7. [DOI] [PubMed] [Google Scholar]
  21. Geiger B., Dutton A. H., Tokuyasu K. T., Singer S. J. Immunoelectron microscope studies of membrane-microfilament interactions: distributions of alpha-actinin, tropomyosin, and vinculin in intestinal epithelial brush border and chicken gizzard smooth muscle cells. J Cell Biol. 1981 Dec;91(3 Pt 1):614–628. doi: 10.1083/jcb.91.3.614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Geiger B., Tokuyasu K. T., Dutton A. H., Singer S. J. Vinculin, an intracellular protein localized at specialized sites where microfilament bundles terminate at cell membranes. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4127–4131. doi: 10.1073/pnas.77.7.4127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Geiger B., Tokuyasu K. T., Singer S. J. Immunocytochemical localization of alpha-actinin in intestinal epithelial cells. Proc Natl Acad Sci U S A. 1979 Jun;76(6):2833–2837. doi: 10.1073/pnas.76.6.2833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Goodenough D. A. Lens gap junctions: a structural hypothesis for nonregulated low-resistance intercellular pathways. Invest Ophthalmol Vis Sci. 1979 Nov;18(11):1104–1122. [PubMed] [Google Scholar]
  25. Goodenough D. A., Revel J. P. A fine structural analysis of intercellular junctions in the mouse liver. J Cell Biol. 1970 May;45(2):272–290. doi: 10.1083/jcb.45.2.272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Goodenough D. A., Stoeckenius W. The isolation of mouse hepatocyte gap junctions. Preliminary chemical characterization and x-ray diffraction. J Cell Biol. 1972 Sep;54(3):646–656. doi: 10.1083/jcb.54.3.646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Gorbsky G., Steinberg M. S. Isolation of the intercellular glycoproteins of desmosomes. J Cell Biol. 1981 Jul;90(1):243–248. doi: 10.1083/jcb.90.1.243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Griepp E. B., Dolan W. J., Robbins E. S., Sabatini D. D. Participation of plasma membrane proteins in the formation of tight junctions by cultured epithelial cells. J Cell Biol. 1983 Mar;96(3):693–702. doi: 10.1083/jcb.96.3.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Hays R. M., Singer B., Malamed S. The effect of calcium withdrawal on the structure and function of the toad bladder. J Cell Biol. 1965 Jun;25(3 Suppl):195–208. doi: 10.1083/jcb.25.3.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Henderson D., Eibl H., Weber K. Structure and biochemistry of mouse hepatic gap junctions. J Mol Biol. 1979 Aug 5;132(2):193–218. doi: 10.1016/0022-2836(79)90391-7. [DOI] [PubMed] [Google Scholar]
  31. Hertzberg E. L., Gilula N. B. Isolation and characterization of gap junctions from rat liver. J Biol Chem. 1979 Mar 25;254(6):2138–2147. [PubMed] [Google Scholar]
  32. Hull B. E., Staehelin L. A. Functional significance of the variations in the geometrical organization of tight junction networks. J Cell Biol. 1976 Mar;68(3):688–704. doi: 10.1083/jcb.68.3.688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Kachar B., Reese T. S. Evidence for the lipidic nature of tight junction strands. Nature. 1982 Apr 1;296(5856):464–466. doi: 10.1038/296464a0. [DOI] [PubMed] [Google Scholar]
  34. Kensler R. W., Goodenough D. A. Isolation of mouse myocardial gap junctions. J Cell Biol. 1980 Sep;86(3):755–764. doi: 10.1083/jcb.86.3.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  36. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  37. MILLER F. Hemoglobin absorption by the cells of the proximal convoluted tubule in mouse kidney. J Biophys Biochem Cytol. 1960 Dec;8:689–718. doi: 10.1083/jcb.8.3.689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Martinez-Palomo A., Meza I., Beaty G., Cereijido M. Experimental modulation of occluding junctions in a cultured transporting epithelium. J Cell Biol. 1980 Dec;87(3 Pt 1):736–745. doi: 10.1083/jcb.87.3.736. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. 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]
  40. Moreno J. H., Diamond J. M. Discrimination of monovalent inorganic cations by "tight" junctions of gallbladder epithelium. J Membr Biol. 1974;15(3):277–318. doi: 10.1007/BF01870092. [DOI] [PubMed] [Google Scholar]
  41. NEVILLE D. M., Jr The isolation of a cell membrane fraction from rat liver. J Biophys Biochem Cytol. 1960 Oct;8:413–422. doi: 10.1083/jcb.8.2.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Pinto da Silva P., Branton D. Membrane splitting in freeze-ethching. Covalently bound ferritin as a membrane marker. J Cell Biol. 1970 Jun;45(3):598–605. doi: 10.1083/jcb.45.3.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Pinto da Silva P., Kachar B. On tight-junction structure. Cell. 1982 Mar;28(3):441–450. doi: 10.1016/0092-8674(82)90198-2. [DOI] [PubMed] [Google Scholar]
  44. Raviola E., Goodenough D. A., Raviola G. Structure of rapidly frozen gap junctions. J Cell Biol. 1980 Oct;87(1):273–279. doi: 10.1083/jcb.87.1.273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. 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]
  46. Skerrow C. J., Matoltsy A. G. Chemical characterization of isolated epidermal desmosomes. J Cell Biol. 1974 Nov;63(2 Pt 1):524–530. doi: 10.1083/jcb.63.2.524. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Skerrow C. J., Matoltsy A. G. Isolation of epidermal desmosomes. J Cell Biol. 1974 Nov;63(2 Pt 1):515–523. doi: 10.1083/jcb.63.2.515. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Skerrow C. J. Selective extraction of desmosomal proteins by low ionic strength media. Biochim Biophys Acta. 1979 Jul 25;579(1):241–245. doi: 10.1016/0005-2795(79)90103-x. [DOI] [PubMed] [Google Scholar]
  49. Song C. S., Rubin W., Rifkind A. B., Kappas A. Plasma membranes of the rat liver. Isolation and enzymatic characterization of a fraction rich in bile canaliculi. J Cell Biol. 1969 Apr;41(1):124–132. doi: 10.1083/jcb.41.1.124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. 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]
  51. Staehelin L. A., Mukherjee T. M., Williams A. W. Freeze-etch appearance of the tight junctions in the epithelium of small and large intestine of mice. Protoplasma. 1969;67(2):165–184. doi: 10.1007/BF01248737. [DOI] [PubMed] [Google Scholar]
  52. Teillet M. A., Hugon J. S., Calvert R. The occluding junctions of mouse duodenal enterocytes during development. A freeze-fracture study. Cell Tissue Res. 1981;217(1):65–77. doi: 10.1007/BF00233827. [DOI] [PubMed] [Google Scholar]
  53. Wade J. B., Karnovsky M. J. The structure of the zonula occludens. A single fibril model based on freeze-fracture. J Cell Biol. 1974 Jan;60(1):168–180. doi: 10.1083/jcb.60.1.168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. van Deurs B., Koehler J. K. Tight junctions in the choroid plexus epithelium. A freeze-fracture study including complementary replicas. J Cell Biol. 1979 Mar;80(3):662–673. doi: 10.1083/jcb.80.3.662. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. van Deurs B., Luft J. H. Effects of glutaraldehyde fixation on the structure of tight junctions: a quantitative freeze-fracture analysis. J Ultrastruct Res. 1979 Aug;68(2):160–172. doi: 10.1016/s0022-5320(79)90151-5. [DOI] [PubMed] [Google Scholar]

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

RESOURCES