Literature DB >> 2416473

Growth inhibition of transformed cells correlates with their junctional communication with normal cells.

P P Mehta, J S Bertram, W R Loewenstein.   

Abstract

The growth of various chemically and virally transformed cell types in culture is inhibited when they are in contact with normal cell types. We show that this growth inhibition is contingent on the presence of junctional communication between the normal and transformed cells (heterologous communication), as probed with a 443 dalton microinjected fluorescent tracer. In cell combinations where heterologous communication is weak or absent there is no detectable growth inhibition; the inhibition appears when communication is induced by cyclic AMP-dependent phosphorylation, and only then. In cell combinations where heterologous communication is spontaneously strong, the growth inhibition is present, but it is abolished when the communication is blocked by retinol or retinoic acid. The cell-to-cell membrane channels of gap junctions are the likely conduits of the signals for this growth control.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 2416473     DOI: 10.1016/0092-8674(86)90497-6

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  85 in total

1.  Interactions between normal mammary epithelial cells and mammary tumour cells in a model system.

Authors:  L H Quarrie; J D Pitts; M E Finbow
Journal:  Cell Prolif       Date:  1999-12       Impact factor: 6.831

2.  Growth retardation in glioma cells cocultured with cells overexpressing a gap junction protein.

Authors:  D Zhu; G M Kidder; S Caveney; C C Naus
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-01       Impact factor: 11.205

3.  Characteristics of C6 glioma cells overexpressing a gap junction protein.

Authors:  C C Naus; D Zhu; S D Todd; G M Kidder
Journal:  Cell Mol Neurobiol       Date:  1992-04       Impact factor: 5.046

Review 4.  Role of retinoid signaling in the regulation of spermatogenesis.

Authors:  S S W Chung; D J Wolgemuth
Journal:  Cytogenet Genome Res       Date:  2004       Impact factor: 1.636

5.  An in vitro model for cell-cell interactions.

Authors:  K B Saunders; P A D'Amore
Journal:  In Vitro Cell Dev Biol       Date:  1992 Jul-Aug

6.  The cellular ecology of progressive neoplastic transformation: a clonal analysis.

Authors:  M Chow; H Rubin
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

7.  The effect of complete carcinogens on intercellular transfer of lucifer yellow in fibroblast culture.

Authors:  I V Budunova; L A Mittelman; G A Belitsky
Journal:  Cell Biol Toxicol       Date:  1990-01       Impact factor: 6.691

Review 8.  Gap junction- and hemichannel-independent actions of connexins.

Authors:  Jean X Jiang; Sumin Gu
Journal:  Biochim Biophys Acta       Date:  2004-10-22

9.  Immunohistochemical localization of connexin 43 in the developing tooth germ of rat.

Authors:  M Kagayama; H Akita; Y Sasano
Journal:  Anat Embryol (Berl)       Date:  1995-06

10.  Acute internalization of gap junctions in vascular endothelial cells in response to inflammatory mediator-induced G-protein coupled receptor activation.

Authors:  Susan M Baker; Namho Kim; Anna M Gumpert; Dominique Segretain; Matthias M Falk
Journal:  FEBS Lett       Date:  2008-11-04       Impact factor: 4.124

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.