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Sphingosine-1-Phosphate A Novel Nonhypoxic Activator of Hypoxia-Inducible Factor-1 in Vascular Cells
被引:54
作者:
Michaud, Maude D.
[1
,2
]
Robitaille, Genevieve A.
[1
,2
]
Gratton, Jean-Philippe
[3
]
Richard, Darren E.
[1
,2
]
机构:
[1] Univ Laval, Hotel Dieu Quebec, Ctr Rech CHUQ, Quebec City, PQ G1R 2J6, Canada
[2] Univ Laval, Dept Med, Quebec City, PQ G1R 2J6, Canada
[3] Univ Montreal, IRCM, Lab Endothelial Cell Biol, Montreal, PQ H3C 3J7, Canada
基金:
加拿大健康研究院;
关键词:
sphingosine;
1-phosphate;
hypoxia-inducible factor-1;
gene expression;
endothelial cells;
vascular smooth muscle cells;
SMOOTH-MUSCLE-CELLS;
SPHINGOSINE;
1-PHOSPHATE;
ENDOTHELIAL-CELLS;
LYSOPHOSPHATIDIC ACID;
INTRACELLULAR ASCORBATE;
TUMOR ANGIOGENESIS;
HIF HYDROXYLASES;
HIF-1-ALPHA;
EXPRESSION;
INDUCTION;
D O I:
10.1161/ATVBAHA.109.185280
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objective-Sphingosine-1-phosphate (S1P) is a potent bioactive phospholipid responsible for a variety of vascular cell responses. Hypoxia-inducible factor-1 (HIF-1) is a transcriptional activator of genes essential for adaptation to low oxygen. S1P and HIF-1 are both important mediators of vascular cell responses such as migation, proliferation, and survival. Studies have shown that nonhypoxic stimuli can activate HIF-1 in oxygenated conditions. Here, we attempt to determine whether S1P can modulate the vascular activation of HIF-1. Methods and Results-We show that in vascular endothelial and smooth muscle cells, activation of the S1P type-2 receptor by S1P strongly increases HIF-1 alpha protein levels, the active subunit of HIF-1. This is achieved through pVHL-independent stabilization of HIF-1 alpha. We demonstrate that the HIF- 1 nuclear complex, formed on S1P stimulation, is transcriptionally active and specifically binds to a hypoxia-responsive elements. Moreover, S1P activates the expression of genes known to be closely regulated by HIF-1. Conclusion-Our results identify S1P as a novel and potent nonhypoxic activator of HIF-1. We believe that understanding the role played by HIF-1 in S1P gene regulation will have a strong impact on different aspects of vascular biology. (Arterioscler Thromb Vasc Biol. 2009; 29:902-908.)
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页码:902 / U302
页数:19
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