Literature DB >> 1667586

Release of H2O2 and phosphorylation of 30 kilodalton proteins as early responses of cell cycle-dependent inhibition of DNA synthesis by transforming growth factor beta 1.

M Shibanuma1, T Kuroki, K Nose.   

Abstract

Transforming growth factor beta 1 (TGF-beta 1) and H2O2 both inhibited DNA synthesis of mouse osteoblastic (MC3T3) cells in the late G1 phase of the cell cycle. TGF-beta 1 stimulated cells to release H2O2 in the late G1 phase, but not in the G0 phase, even though TGF-beta 1 receptors were present in both phases. The inhibition of DNA synthesis caused by TGF-beta 1 was partly decreased by the addition of catalase. TGF-beta 1 and H2O2 increased the phosphorylation of the same proteins with a molecular weight of 30,000 in cells in the late G1 phase, and the increase by TGF-beta 1 was abolished at least partly by catalase. The results suggest that H2O2 is one of the mediators of inhibition of DNA synthesis by TGF-beta 1.

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Year:  1991        PMID: 1667586

Source DB:  PubMed          Journal:  Cell Growth Differ        ISSN: 1044-9523


  4 in total

1.  Activation of hepatic stellate cells by TGF alpha and collagen type I is mediated by oxidative stress through c-myb expression.

Authors:  K S Lee; M Buck; K Houglum; M Chojkier
Journal:  J Clin Invest       Date:  1995-11       Impact factor: 14.808

2.  Effect of radical scavengers on TNF alpha-mediated activation of the uPA in cultured cells.

Authors:  K Egawa; M Yoshiwara; K Nose
Journal:  Experientia       Date:  1994-10-15

Review 3.  Oxidative stress and glutathione in TGF-beta-mediated fibrogenesis.

Authors:  R-M Liu; K A Gaston Pravia
Journal:  Free Radic Biol Med       Date:  2009-10-02       Impact factor: 7.376

4.  Production of hydrogen peroxide by transforming growth factor-beta 1 and its involvement in induction of egr-1 in mouse osteoblastic cells.

Authors:  M Ohba; M Shibanuma; T Kuroki; K Nose
Journal:  J Cell Biol       Date:  1994-08       Impact factor: 10.539

  4 in total

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