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Blood, 15 March 2006, Vol. 107, No. 6, pp. 2322-2329.
Prepublished online as a Blood First Edition Paper on September 27, 2005; DOI 10.1182/blood-2005-06-2377.
Previous Article | Next Article 
Submitted June 16, 2005
Accepted September 15, 2005
Inducible platelet-derived growth factor D-chain expression by angiotensin II and hydrogen peroxide involves transcriptional regulation by Ets-1 and Sp1
Mary Y Liu, Melanie Eyries, Chunyan Zhang, Fernando S Santiago, and Levon M Khachigian*
Centre for Vascular Research, Department of Pathology, University of New South Wales and the Department of Haematology, Prince of Wales Hospital, Sydney, NSW, Australia
* Corresponding author; email: L.Khachigian{at}unsw.edu.au.
Platelet-derived growth factor D-chain (PDGF-D) is the newest member of the PDGF family of mitogens and chemoattractants expressed in a wide variety of cell types, including vascular smooth muscle cells (SMCs). The molecular mechanisms regulating PDGF-D transcription are not known. Primer extension analysis mapped a single transcriptional start site to the ccAGCGC motif with several potential Ets motifs located upstream. Ets-1, but not Ets-1 bearing only the DNA-binding domain, activates the PDGF-D promoter and mRNA expression in SMCs. Ets site D3 (-470GGAT-467) is singly required for basal and Ets-1-inducible PDGF-D promoter-dependent expression. D3 supports the interaction of endogenous and recombinant Ets-1 and Sp1. Sp1, like Ets-1, induces PDGF-D transcription and mRNA expression, which is blocked by mutant Ets-1. Hydrogen peroxide stimulates Ets-1 but not Sp1, and activates D3-dependent PDGF-D transcription. Ets-1 and Sp1 siRNA block peroxide-inducible PDGF-D expression. Angiotensin II (ATII) induction of PDGF-D and Ets-1 were blocked by prior incubation of the cells with PEG-catalase, but not BSA indicating that ATII-inducible Ets-1 and PDGF-D expression is mediated via H2O2. Thus, two separate trans-acting factors regulate PDGF-D transcription, alone and in response to oxidative stress.

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