Literature DB >> 12039986

Transcription factor Ets-1 regulates gelatinase a gene expression in mesangial cells.

Julia Reisdorff1, Abdelaziz En-Nia, Ioannis Stefanidis, Jürgen Floege, David H Lovett, Peter R Mertens.   

Abstract

Ets transcription factors are involved in cell growth and angiogenesis. Ets-1 targets include members of the matrix metalloproteinase superfamily. In inflammatory glomerular diseases, the patterns and regulation of Ets expression have not been fully characterized. In the present study, nuclear binding activities to the consensus Ets-1/PEA3 motif were detected in mesangial cells (MC), and the Ets-1 protein was positively identified by Western blotting, reverse transcription PCR (RT-PCR), and DNA-binding studies. The 5' flanking regions of the human and rat gelatinase A genes contain clusters of potential Ets-1 binding motifs, one of which is evolutionarily conserved. Using a series of 5' deletion reporter constructs of the rat gelatinase A gene and an Ets-1 expression plasmid, a concentration-dependent threefold trans-activation of gene expression mapped to the conserved Ets-1 binding motif at -1004/-1053 bps, designated responsive element-2 (RE-2). The RE-2 was operative within the context of the homologous gelatinase A promoter but not with a heterologous simian virus 40 promoter. Specific Ets-1 binding to this sequence was demonstrated by DNA-binding studies. Transient expression of an Ets-1 expression plasmid increased gelatinase A protein expression. Our findings identify an additional matrix metalloproteinase family member, gelatinase A, as an Ets-1 responsive gene in MC that may play a role in the high level expression of this enzyme in inflammatory glomerular diseases.

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Year:  2002        PMID: 12039986     DOI: 10.1097/01.asn.0000015617.39974.fb

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  5 in total

1.  Inhibitory effects of the transcription factor Ets-1 on the expression of type I collagen in TGF-β1-stimulated renal epithelial cells.

Authors:  Kazuhiro Okano; Asako Hibi; Tokiko Miyaoka; Tomoko Inoue; Himiko Sugimoto; Ken Tsuchiya; Takashi Akiba; Kosaku Nitta
Journal:  Mol Cell Biochem       Date:  2012-07-25       Impact factor: 3.396

2.  Ets1 blocks terminal differentiation of keratinocytes and induces expression of matrix metalloproteases and innate immune mediators.

Authors:  Priyadharsini Nagarajan; Shu Shien Chin; Dan Wang; Song Liu; Satrajit Sinha; Lee Ann Garrett-Sinha
Journal:  J Cell Sci       Date:  2010-10-15       Impact factor: 5.285

3.  Evidence for the involvement of p38 MAP kinase in the action of the vascular disrupting agent 5,6-dimethylxanthenone-4-acetic acid (DMXAA).

Authors:  Liangli Zhao; Elaine S Marshall; Lloyd R Kelland; Bruce C Baguley
Journal:  Invest New Drugs       Date:  2007-01-03       Impact factor: 3.651

4.  Cold shock Y-box protein-1 proteolysis autoregulates its transcriptional activities.

Authors:  Claudia R C van Roeyen; Florian G Scurt; Sabine Brandt; Vanessa A Kuhl; Sandra Martinkus; Sonja Djudjaj; Ute Raffetseder; Hans-Dieter Royer; Ioannis Stefanidis; Sandra E Dunn; Steven Dooley; Honglei Weng; Thomas Fischer; Jonathan A Lindquist; Peter R Mertens
Journal:  Cell Commun Signal       Date:  2013-08-27       Impact factor: 5.712

5.  Ets1 induces dysplastic changes when expressed in terminally-differentiating squamous epidermal cells.

Authors:  Priyadharsini Nagarajan; Neha Parikh; Lee Ann Garrett-Sinha; Satrajit Sinha
Journal:  PLoS One       Date:  2009-01-14       Impact factor: 3.240

  5 in total

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