Literature DB >> 219290

Ultrastructural, biochemical, and immunologic characterization of Mallory bodies in livers of griseofulvin-treated mice. Fimbriated rods of filaments containing prekeratin-like polypeptides.

W W Franke, H Denk, E Schmid, M Osborn, K Weber.   

Abstract

Mallory bodies (MBs) induced in hepatocytes by long term feeding of mice with griseofulvin were isolated, purified, and examined by electron microscopy in ultrathin sections and negatively stained preparations. The major structural component of the MBs was randomly oriented, unbranched rods of filaments; these were usually 175 to 250 nm. long and 14 to 20 nm. thick and covered by a dense fimbriate coat of laterally projecting 1.5- to 3-nm. thick threads. Such lateral threads could extend for more than 20 nm. and seemed to be involved in the interconnection of adjacent filaments and their association and aggregation into MBs. Using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the purified filament material showed six major polypeptide bands with apparent molecular weights ranging from 48,000 to 66,000. When the portion of the MB filament material that was soluble in solutions containing 8 M urea was allowed to reaggregate upon removal of the urea, an enrichment of one of the polypeptide components (approximate molecular weight, 64,000) was observed. When frozen sections of liver tissue MBs were subjected to indirect immunofluorescence microscopy, they were specifically revealed by guinea pig antibodies directed against purified bovine prekeratin. No significant accumulation of MBs was observed with a series of other antisera, including those containing antibodies against tubulin, actin, and vimentin, the major protein of the intermediate sized filaments predominant in mesenchymal cells. The observations suggest that MBs in livers of griseofulvin-treated mice, and probably also of human alcoholic hepatitis, contain large amounts of prekeratin-like polypeptides which are assembled into a special form of fimbriated rods of 14- to 20-nm. filaments. These filaments are morphologically different from other forms of intermediate sized and thick filaments, including the prekeratin-containing 6- to 11-nm. tonofilament-like filaments present in various epithelial cells.

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Year:  1979        PMID: 219290

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  23 in total

Review 1.  The role of the ubiquitin proteasome pathway in keratin intermediate filament protein degradation.

Authors:  Micah R Rogel; Ariel Jaitovich; Karen M Ridge
Journal:  Proc Am Thorac Soc       Date:  2010-02

2.  Mallory body filaments become insoluble after normal assembly into intermediate filaments.

Authors:  M S Pollanen; P Markiewicz; L Weyer; M C Goh; C Bergeron
Journal:  Am J Pathol       Date:  1994-11       Impact factor: 4.307

3.  Hepatocyte cytokeratins are hyperphosphorylated at multiple sites in human alcoholic hepatitis and in a mallory body mouse model.

Authors:  C Stumptner; M B Omary; P Fickert; H Denk; K Zatloukal
Journal:  Am J Pathol       Date:  2000-01       Impact factor: 4.307

4.  Selective presence of ubiquitin in intracellular inclusions.

Authors:  V Manetto; F W Abdul-Karim; G Perry; M Tabaton; L Autilio-Gambetti; P Gambetti
Journal:  Am J Pathol       Date:  1989-03       Impact factor: 4.307

5.  Isolation of Mallory bodies and an attempt to demonstrate cell mediated immunity to Mallory body isolate in patients with alcoholic liver disease.

Authors:  C Gluud; F Hardt; J Aldershvile; P Christoffersen; H Lyon; J Nielsen
Journal:  J Clin Pathol       Date:  1981-09       Impact factor: 3.411

6.  Cytoarchitectural analysis of epithelial sheets formed in vitro by hepatic tumor cells possessing defined intermediate-sized filament cytoskeletal abnormalities.

Authors:  M P Ryan; E Borenfreund; P J Higgins
Journal:  Am J Pathol       Date:  1989-02       Impact factor: 4.307

7.  Mallory bodies: lesions of hepatocytes containing proteins of the keratin-myosin-epidermin group.

Authors:  S N Meloan; H Puchtler
Journal:  Histochemistry       Date:  1982

8.  Mallory bodies in alcoholic liver disease: identification of cytoplasmic filament/cell membrane and unique antigenic determinants by monoclonal antibodies.

Authors:  J A Morton; J Bastin; K A Fleming; A McMichael; J Burns; J O McGee
Journal:  Gut       Date:  1981-01       Impact factor: 23.059

9.  A cell culture system for the induction of Mallory bodies: Mallory bodies and aggresomes represent different types of inclusion bodies.

Authors:  Kiyoko Hirano; Bruno Guhl; Jürgen Roth; Martin Ziak
Journal:  Histochem Cell Biol       Date:  2009-04-18       Impact factor: 4.304

Review 10.  Histopathology of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis.

Authors:  Gregory Thomas Brown; David E Kleiner
Journal:  Metabolism       Date:  2015-12-02       Impact factor: 8.694

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