Literature DB >> 12859960

A dominant negative TAK1 inhibits cellular fibrotic responses induced by TGF-beta.

Koichiro Ono1, Toshihiko Ohtomo, Jun Ninomiya-Tsuji, Masayuki Tsuchiya.   

Abstract

Transforming growth factor-beta (TGF-beta) is crucially virulent in the progression of fibrotic disorders. TAK1 (TGF-beta activated kinase 1) is one of the mitogen-activated kinase kinase kinase (MAPKKK) that is involved in TGF-beta signal transduction. To elucidate the importance of TAK1 in TGF-beta-induced fibrotic marker expression, we investigated whether dominant negative TAK1 could suppress TGF-beta signaling. Based on the finding that TAB1 (TAK1 binding protein 1) binding to TAK1 is required for TAK1 activation, a minimal portion of TAK1 lacking kinase activity that binds to TAB1 was designed as a TAK1 dominant negative inhibitor (TAK1-DN). The effect of TAK1-DN was assessed in the cells that respond to TGF-beta stimulation and that lead to the increase in production of extracellular matrix (ECM) proteins. TAK1-DN, indeed, decreased the ECM protein production, indicating that TAK1-DN retains the ability to intercept the TGF-beta signaling effectively.

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Year:  2003        PMID: 12859960     DOI: 10.1016/s0006-291x(03)01207-5

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  30 in total

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Review 5.  Regulation of autophagy by TGF-β: emerging role in kidney fibrosis.

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Review 9.  TGF-β signaling in the kidney: profibrotic and protective effects.

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Review 10.  TGF-β signaling via TAK1 pathway: role in kidney fibrosis.

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