TNF-α Stimulation of MCP-1 Expression Is Mediated by the Akt/PKB Signal Transduction Pathway in Vascular Endothelial Cells
MCP-1 is expressed in a variety of cell types including vascular endothelial cells following induction by different stimuli such as tumor necrosis factor (TNF)-α. Although TNF-α stimulates MCP-1 expression and secretion, the mechanism by which TNF-α stimulates expression of the MCP-1 gene is not kno...
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Veröffentlicht in: | Biochemical and biophysical research communications 2000-09, Vol.276 (2), p.791-796 |
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Sprache: | eng |
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Zusammenfassung: | MCP-1 is expressed in a variety of cell types including vascular endothelial cells following induction by different stimuli such as tumor necrosis factor (TNF)-α. Although TNF-α stimulates MCP-1 expression and secretion, the mechanism by which TNF-α stimulates expression of the MCP-1 gene is not known. In this study, we examine the involvement of the phosphatidylinositol-3-OH kinase (PI3-kinase)-Akt/PKB pathway. Exposure of human umbilical vein endothelial cells (HUVECs) to TNF-α elicited the rapid phosphorylation of Akt/PKB. In HUVECs, wortmannin, a PI3-kinase inhibitor, inhibits TNF-α-mediated MCP-1 secretion at a dose-dependent manner. Constitutively active form of Akt/PKB induces transcription of the MCP-1 gene, and cotransfection of dominant negative Akt/PKB suppressed the activation of the MCP-1 promoter induced by TNF-α. These findings show that Akt/PKB participates in the TNF-α induction of MCP-1 gene transcription in endothelial cells. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1006/bbrc.2000.3497 |