Literature DB >> 794589

Localization and organization of microfilaments and related proteins in normal and virus-transformed cells.

R D Goldman, M J Yerna, J A Schloss.   

Abstract

The localization and organization of actin-like microfilaments in normal, SV-40 and adenovirus transformed cells are determined by the coordinated use of light optical, electron optical and biochemical techniques. In adenovirus-type 5 transformed hamster embryo cells, microfilament meshworks appear to be the predominant organizational form of cellular action, while in normal hamster cells, microfilament bundles are prevalent. Differences between 3T3 and SV-40 transformed 3T3 cells are less apparent and may be related to the packing and intracellular distribution of microfilament bundles. Attempts at relating these ultrastructural changes in transformed cells to the images obtained following reaction with fluorescein-labelled myosin fragments and indirect immunofluorescence with smooth muscle myosin antibody are discussed. In several instances the fluorescence microscope images to not correspond to the ultrastructural observations. The results are discussed in terms of the possible relationships between alterations in cytoplasmic contractile elements and the abnormal behavior of transformed cells.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 794589     DOI: 10.1002/jss.400050206

Source DB:  PubMed          Journal:  J Supramol Struct        ISSN: 0091-7419


  24 in total

1.  Relationship between organization of the actin cytoskeleton and the cell cycle in normal and adenovirus-infected rat cells.

Authors:  P Jackson; A J Bellett
Journal:  J Virol       Date:  1989-01       Impact factor: 5.103

2.  Immunolocalization in three dimensions: immunogold staining of cytoskeletal and nuclear matrix proteins in resinless electron microscopy sections.

Authors:  J A Nickerson; G Krockmalnic; D C He; S Penman
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

3.  Evidence for unaltered structure and in vivo assembly of microtubules in transformed cells.

Authors:  J De Mey; M Joniau; M De Brabander; W Moens; G Geuens
Journal:  Proc Natl Acad Sci U S A       Date:  1978-03       Impact factor: 11.205

4.  Molecular cytochemistry: incorporation of fluorescently labeled actin into living cells.

Authors:  D L Taylor; Y L Wang
Journal:  Proc Natl Acad Sci U S A       Date:  1978-02       Impact factor: 11.205

5.  Morphological evidence for cyclic AMP-induced reverse transformation in vole cells infected with avian sarcoma virus.

Authors:  W D Meek
Journal:  Mol Cell Biol       Date:  1982-07       Impact factor: 4.272

Review 6.  Rethinking cell structure.

Authors:  S Penman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-06       Impact factor: 11.205

7.  A novel protein accumulated during maturation of the pods of the plant Impatiens balsamina.

Authors:  M Pal; S Biswas
Journal:  Mol Cell Biochem       Date:  1994-01-26       Impact factor: 3.396

8.  Altered distributions of the cytoskeletal proteins vinculin and alpha-actinin in cultured fibroblasts transformed by Rous sarcoma virus.

Authors:  T David-Pfeuty; S J Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

9.  Distribution of actin in migrating leukocytes in vivo.

Authors:  J J Wolosewick
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

10.  Cytoskeletal F-actin patterns quantitated with fluorescein isothiocyanate-phalloidin in normal and transformed cells.

Authors:  M Verderame; D Alcorta; M Egnor; K Smith; R Pollack
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.