Literature DB >> 6425301

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

B R Stevenson, D A Goodenough.   

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.

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Year:  1984        PMID: 6425301      PMCID: PMC2113227          DOI: 10.1083/jcb.98.4.1209

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  55 in total

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Authors:  G Fairbanks; T L Steck; D F Wallach
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2.  Freeze-etch appearance of the tight junctions in the epithelium of small and large intestine of mice.

Authors:  L A Staehelin; T M Mukherjee; A W Williams
Journal:  Protoplasma       Date:  1969       Impact factor: 3.356

3.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
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4.  Fracture faces of frozen membranes.

Authors:  D Branton
Journal:  Proc Natl Acad Sci U S A       Date:  1966-05       Impact factor: 11.205

5.  Membrane splitting in freeze-ethching. Covalently bound ferritin as a membrane marker.

Authors:  P Pinto da Silva; D Branton
Journal:  J Cell Biol       Date:  1970-06       Impact factor: 10.539

6.  Hexagonal array of subunits in tight junctions separated from isolated rat liver plasma membranes.

Authors:  E L Benedetti; P Emmelot
Journal:  J Cell Biol       Date:  1968-07       Impact factor: 10.539

7.  Plasma membranes of the rat liver. Isolation and enzymatic characterization of a fraction rich in bile canaliculi.

Authors:  C S Song; W Rubin; A B Rifkind; A Kappas
Journal:  J Cell Biol       Date:  1969-04       Impact factor: 10.539

8.  Cellular mechanism of intestinal permeability alterations produced by chelation depletion.

Authors:  M M Cassidy; C S Tidball
Journal:  J Cell Biol       Date:  1967-03       Impact factor: 10.539

9.  The effect of calcium withdrawal on the structure and function of the toad bladder.

Authors:  R M Hays; B Singer; S Malamed
Journal:  J Cell Biol       Date:  1965-06       Impact factor: 10.539

10.  High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study.

Authors:  M N Berry; D S Friend
Journal:  J Cell Biol       Date:  1969-12       Impact factor: 10.539

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  46 in total

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Review 6.  Molecular basis of the core structure of tight junctions.

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7.  Phosphorylation of the tight-junction protein ZO-1 in two strains of Madin-Darby canine kidney cells which differ in transepithelial resistance.

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Review 8.  The epithelial tight junction: structure, function and preliminary biochemical characterization.

Authors:  B R Stevenson; J M Anderson; S Bullivant
Journal:  Mol Cell Biochem       Date:  1988-10       Impact factor: 3.396

9.  Deposition of BaSO4 in the tight junctions of amphibian epithelia causes their opening; apical Ca2+ reverses this effect.

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