Literature DB >> 6273447

Rapid and reversible reduction of junctional permeability in cells infected with a temperature-sensitive mutant of avian sarcoma virus.

M M Atkinson, A S Menko, R G Johnson, J R Sheppard, J D Sheridan.   

Abstract

The transformed or normal phenotype of cultured normal rat kidney cells infected with a temperature-sensitive mutant of avian sarcoma virus is conditional on the temperature at which the cells are grown. Using dye injection techniques, we show that junction-mediated dye transfer is also temperature-sensitive. The extent and rate of transfer between infected cells grown at the transformation-permissive temperature (35 degrees C) is significantly reduced when compared to infected cells grown at the nonpermissive temperature (40.5 degrees C) or uninfected cells grown at either temperature. Infected cells subjected to reciprocal temperature shifts express rapid and reversible alterations of dye transfer capacities, with responses evident by 15 min and completed by 60 min for temperature shifts in either direction. These results suggest that altered junctional capacities may be fundamental to the expression of the ASV-induced, transformed phenotype.

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Year:  1981        PMID: 6273447      PMCID: PMC2111987          DOI: 10.1083/jcb.91.2.573

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


  23 in total

1.  Differential induction of tumour antigens by transformation-defective virus mutants.

Authors:  R Kurth
Journal:  J Gen Virol       Date:  1975-08       Impact factor: 3.891

2.  Permeability of cell junction depends on local cytoplasmic calcium activity.

Authors:  B Rose; W R Loewenstein
Journal:  Nature       Date:  1975-03-20       Impact factor: 49.962

3.  Low resistance junctions between normal and between virus transformed fibroblasts in tissue culture.

Authors:  P O'Lague; H Dalen
Journal:  Exp Cell Res       Date:  1974-06       Impact factor: 3.905

4.  Junctions between cancer cells in culture: ultrastructure and permeability.

Authors:  R G Johnson; J D Sheridan
Journal:  Science       Date:  1971-11-12       Impact factor: 47.728

5.  Gap junction formation between reaggregated Novikoff hepatoma cells.

Authors:  R Johnson; M Hammer; J Sheridan; J P Revel
Journal:  Proc Natl Acad Sci U S A       Date:  1974-11       Impact factor: 11.205

6.  The selective isolation of temperature-sensitive mutants of Rous sarcoma virus.

Authors:  J A Wyke
Journal:  Virology       Date:  1973-04       Impact factor: 3.616

7.  Cellular communication, contact inhibition, cell clocks, and cancer: the impact of the work and ideas of W. R. Loewenstein.

Authors:  A C Burton
Journal:  Perspect Biol Med       Date:  1971       Impact factor: 1.416

8.  Differences in intracellular location of pp60src in rat and chicken cells transformed by Rous sarcoma virus.

Authors:  J G Krueger; E Wang; E A Garber; A R Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

9.  Phosphorylation of pp60src and the cycloheximide insensitive activation of the pp60src-associated kinase activity of transformation-defective temperature-sensitive mutants of Rous sarcoma virus.

Authors:  A Ziemiecki; R R Friis
Journal:  Virology       Date:  1980-10-30       Impact factor: 3.616

10.  Low-resistance junctions in epithelial outgrowths from normal and cancerous epidermis in vitro.

Authors:  B A Flaxman; F V Cavoto
Journal:  J Cell Biol       Date:  1973-07       Impact factor: 10.539

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  54 in total

1.  Mechanism of v-Src- and mitogen-activated protein kinase-induced reduction of gap junction communication.

Authors:  G Trevor Cottrell; Rui Lin; Bonnie J Warn-Cramer; Alan F Lau; Janis M Burt
Journal:  Am J Physiol Cell Physiol       Date:  2002-10-16       Impact factor: 4.249

2.  Inhibition of intercellular communication by airborne particulate matter.

Authors:  G A Heussen
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

Review 3.  Connexin43 cardiac gap junction remodeling: lessons from genetically engineered murine models.

Authors:  Benjamin F Remo; Steven Giovannone; Glenn I Fishman
Journal:  J Membr Biol       Date:  2012-06-22       Impact factor: 1.843

4.  Incorporation of the gene for a cell-cell channel protein into transformed cells leads to normalization of growth.

Authors:  P P Mehta; A Hotz-Wagenblatt; B Rose; D Shalloway; W R Loewenstein
Journal:  J Membr Biol       Date:  1991-12       Impact factor: 1.843

5.  Regulation of Connexin32 by ephrin receptors and T-cell protein-tyrosine phosphatase.

Authors:  Andrew J Trease; Hanjun Li; Gaelle Spagnol; Li Zheng; Kelly L Stauch; Paul L Sorgen
Journal:  J Biol Chem       Date:  2018-11-06       Impact factor: 5.157

6.  Expression of the gap junction protein connexin43 in embryonic chick lens: molecular cloning, ultrastructural localization, and post-translational phosphorylation.

Authors:  L S Musil; E C Beyer; D A Goodenough
Journal:  J Membr Biol       Date:  1990-06       Impact factor: 1.843

7.  PKC phosphorylation disrupts gap junctional communication at G0/S phase in clone 9 cells.

Authors:  S K Koo; D Y Kim; S D Park; K W Kang; C O Joe
Journal:  Mol Cell Biochem       Date:  1997-02       Impact factor: 3.396

Review 8.  Junctional communication and cellular differentiation.

Authors:  J D Pitts; M E Finbow; E Kam
Journal:  Br J Cancer Suppl       Date:  1988-12

9.  Potential role of the src gene product in inhibition of gap-junctional communication in NIH/3T3 cells.

Authors:  C C Chang; J E Trosko; H J Kung; D Bombick; F Matsumura
Journal:  Proc Natl Acad Sci U S A       Date:  1985-08       Impact factor: 11.205

10.  Modification of gap junctions in cells transformed by a temperature-sensitive mutant of Rous sarcoma virus.

Authors:  M M Atkinson; S K Anderson; J D Sheridan
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

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