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on July 29, 2004

Arteriosclerosis, Thrombosis, and Vascular Biology. 2004
Published online before print July 29, 2004, doi: 10.1161/01.ATV.0000140819.81839.0e
A more recent version of this article appeared on October 1, 2004
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Submitted on May 18, 2004
Accepted on June 19, 2004

Expression of Angiopoietin-2 in Endothelial Cells is Controlled by Positive and Negative Regulatory Promoter Elements

Anja Hegen ; Stefanie Koidl ; Karin Weindel ; Dieter Marmé ; Hellmut G. Augustin *; and Ulrike Fiedler

From the Department of Vascular Biology and Angiogenesis Research, Tumor Biology Center, D-79106 Freiburg, Germany

* To whom correspondence should be addressed. E-mail: augustin{at}angiogenese.de.

Objective--Angiopoietin-2 (Ang-2) is a non-signal transducing ligand of the endothelial receptor tyrosine kinase Tie-2. Ang-2 is produced by endothelial cells and acts as an autocrine regulator mediating vascular destabilization by inhibiting Angiopoietin-1-mediated Tie-2 activation. To examine the transcriptional regulation of Ang-2, we studied the Ang-2 promoter in endothelial cells and nonendothelial cells.

Methods and Results--The human Ang-2 promoter contains a 585-bp region around the transcriptional start site (-109 to +476) that is sufficient to control endothelial cell-specific and cytokine-dependent Ang-2 expression. Strong repressor elements of Ang-2-promoter activity are located in the 5'-region of the promoter and in the first intron. The Ets family transcription factors Ets-1 and Elf-1 act as strong enhancers of endothelial cell Ang-2-promoter activity. Ets-binding sites -4 and -7 act as positive regulators, whereas Ets-binding site -3 acts as negative regulator. Demethylation experiments revealed that the Ang-2 gene (in contrast to the Tie-2 gene) is not controlled by imprinting.

Conclusions--The data determine unique positive and negative regulatory mechanisms of endothelial cell Ang-2 expression and provide further evidence for the critical role of Ang-2 as a key autocrine regulator of vascular stability and responsiveness.


Key words: angiogenesis • Ang-2 • Ets-1 • Elf-1 • endothelial cell




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