Literature DB >> 7372718

Protein synthesis in transformed 3T3 cells permeabilized by exogenous ATP.

T Kitagawa.   

Abstract

Exogenous ATP has been shown to cause a rapid and reversible increase in permeability in transformed 3T3 cells (3T6 and SV3T3) but not in untransformed 3T3 cells. The cells remain viable, but lose intracellular acid-soluble pools. Treatment of transformed cells with ATP greatly reduces incorporation of 14C-leucine into protein, which is restored by the incubation of the cells with Dulbecco's modified Eagle's medium or by the external additions of certain ions and energy sources. tRNA is not required for the restoration of protein synthesis. In the permeabilized cells the energy for protein synthesis can be provided by glycolysis, oxidative phosphorylation, or direct addition of ATP. These studies demonstrate the usefulness of this method for studying the control of metabolism and macromolecular synthesis in monolayer cultures of transformed mammalian cells.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7372718     DOI: 10.1002/jcp.1041020106

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  4 in total

Review 1.  Permeabilization of transformed cells in culture by external ATP.

Authors:  L A Heppel; G A Weisman; I Friedberg
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

2.  Glucose contribution to nucleic acid base synthesis in proliferating hepatoma cells: a glycine-biosynthesis-mediated pathway.

Authors:  H Bismut; M Caron; C Coudray-Lucas; J Capeau
Journal:  Biochem J       Date:  1995-06-15       Impact factor: 3.857

3.  The potential of nucleotide analogs as inhibitors of retroviruses and tumors.

Authors:  R K Robins
Journal:  Pharm Res       Date:  1984-01       Impact factor: 4.200

4.  Modulation of membrane permeability, cell proliferation and cytotoxicity of antitumor agents by external ATP in mouse tumor cells.

Authors:  T Mure; K Sano; T Kitagawa
Journal:  Jpn J Cancer Res       Date:  1992-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.