» Articles » PMID: 8985745

Disturbed Structural Interactions Between Microfilaments and Tight Junctions in Rat Hepatocytes During Extrahepatic Cholestasis Induced by Common Bile Duct Ligation

Overview
Publisher Springer
Date 1996 Dec 1
PMID 8985745
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Microfilaments in epithelial cells are important for the structural and functional integrity of tight junctions. In the present study, we examined the relationship between microfilaments and tight junctions in hepatocytes of rat liver following common bile duct ligation (CBDL) for up to 2 weeks. Actin filaments and tight junctions were studied by fluorescence microscopy using 7-nitrobenzene-2-oxa-1,3-diazole phallacidin (NBD-ph) and an anti-ZO-1 antibody, respectively. Double-stained sections were examined with confocal laser scanning microscopy (CLSM). Electron microscopy was applied for the assessment of structural alterations in microfilaments and in tight junctions with detergent-extraction and freeze-fracture preparations. Our results showed that F-actin was present at the entire plasma membrane of hepatocytes in control liver, whereas CBDL increased the amount of F-actin mainly at the bile canalicular and lateral plasma membranes. Simultaneously, the immunofluorescence of ZO-1 underwent striking changes, i.e., from a uniform to an irregular staining pattern with various fluorescence intensities. CLSM demonstrated a colocalization of ZO-1 and F-actin in control liver and its deterioration in CBDL liver. Electron microscopy showed marked alterations of microfilaments and tight junctions due to CBDL. It is concluded that actin filaments are intimately associated with tight junctions in normal hepatocytes. CBDL impairs this association by progressively diminishing the structural interaction between F-actin and ZO-1, which may in turn lead to functional disturbances of tight junctions.

Citing Articles

Hepatocyte apical bulkheads provide a mechanical means to oppose bile pressure.

Bebelman M, Bovyn M, Mayer C, Delpierre J, Naumann R, Martins N J Cell Biol. 2023; 222(4).

PMID: 36716168 PMC: 9930133. DOI: 10.1083/jcb.202208002.


Dynamic localization of hepatocellular transporters in health and disease.

Roma M, Crocenzi F, Mottino A World J Gastroenterol. 2008; 14(44):6786-801.

PMID: 19058304 PMC: 2773873. DOI: 10.3748/wjg.14.6786.


Hepatocyte cytoskeleton during ischemia and reperfusion--influence of ANP-mediated p38 MAPK activation.

Keller M, Gerbes A, Kulhanek-Heinze S, Gerwig T, Grutzner U, van Rooijen N World J Gastroenterol. 2006; 11(47):7418-29.

PMID: 16437711 PMC: 4725179. DOI: 10.3748/wjg.v11.i47.7418.


Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses.

Song J, Ichtchenko K, Sudhof T, Brose N Proc Natl Acad Sci U S A. 1999; 96(3):1100-5.

PMID: 9927700 PMC: 15357. DOI: 10.1073/pnas.96.3.1100.

References
1.
Kawahara H, French S . Role of cytoskeleton in canalicular contraction in cultured differentiated hepatocytes. Am J Pathol. 1990; 136(3):521-32. PMC: 1877500. View

2.
Elias E, HRUBAN Z, Wade J, Boyer J . Phalloidin-induced cholestasis: a microfilament-mediated change in junctional complex permeability. Proc Natl Acad Sci U S A. 1980; 77(4):2229-33. PMC: 348686. DOI: 10.1073/pnas.77.4.2229. View

3.
Staddon J, Herrenknecht K, Smales C, Rubin L . Evidence that tyrosine phosphorylation may increase tight junction permeability. J Cell Sci. 1995; 108 ( Pt 2):609-19. DOI: 10.1242/jcs.108.2.609. View

4.
Anderson J, Balda M, Fanning A . The structure and regulation of tight junctions. Curr Opin Cell Biol. 1993; 5(5):772-8. DOI: 10.1016/0955-0674(93)90024-k. View

5.
Watanabe S, Phillips M . Ca2+ causes active contraction of bile canaliculi: direct evidence from microinjection studies. Proc Natl Acad Sci U S A. 1984; 81(19):6164-8. PMC: 391880. DOI: 10.1073/pnas.81.19.6164. View