4.5 Article

Suppression of Tie-1 in endothelial cells in vitro induces a change in the genome-wide expression profile reflecting an inflammatory function

Journal

FEBS LETTERS
Volume 583, Issue 6, Pages 1023-1028

Publisher

WILEY
DOI: 10.1016/j.febslet.2009.02.027

Keywords

Tie-1; Endothelial inflammation; Microarray; U937

Funding

  1. NIDDK Mentored Research Scientist Development Award [1K01DK077727]
  2. Beth Israel Deaconess Medical Center

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Tie-1 is an endothelial specific receptor tyrosine kinase that is upregulated in diseases such as atherosclerosis and rheumatoid arthritis. We recently demonstrated that Tie-1 induced a proinflammatory response when overexpressed in endothelial cells. Here, we used a complementary approach and suppressed endogenous Tie-1 expression in endothelial cells to examine its function by microarray analysis. Tie-1 appeared to govern expression of many genes involved in inflammation. Expression knockdown of Tie-1 significantly reduced endothelial conditioned medium ability to stimulate MCP-1 production in U937 cells. Collectively, our results support the notion that Tie-1 has an inflammatory function in endothelial cells. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

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