Hypoxia and hypoxia-inducible factor-1α promote growth factor-induced proliferation of human vascular smooth muscle cells
Hypoxia and hypoxia-inducible factor-1α promote growth factor-induced proliferation of human vascular smooth muscle cells
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DOI：
10.1152/ajpheart.01077.2005
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发表时间：
2006-06-01
影响因子：
4.8
通讯作者：
Beasley, Debbie
中科院分区：
文献类型：
--
作者：
Schultz, Kelly;Fanburg, Barry L.;Beasley, Debbie
Hypoxia is thought to be a stimulus for the excessive proliferation of vascular smooth muscle cells (VSMC) that contributes to pulmonary hypertension, but the mechanisms involved are unknown. Here we tested whether hypoxia-inducible factor 1-alpha (HIF-1 alpha), a master regulator of the transcriptional response to hypoxia, is involved in the enhanced mitogen-induced proliferative responses of hypoxic VSMC. Exposure to moderate hypoxia (5% O-2) enhanced the proliferative responses of human pulmonary artery SMC (HPASMC) to mitogens including platelet-derived growth factor (PDGF), fibroblast growth factor 2 (FGF-2), and epidermal growth factor (EGF), compared with those in normoxia (20% O-2). Moderate hypoxia elicited increased cellular HIF-1 alpha levels, shown by Western blot analysis, and also enhanced PDGF-, FGF-2-, and EGF-induced expression of HIF-1 alpha. Knockdown of HIF-1 alpha or HIF-1 alpha levels in HPASMC with specific small interfering RNAs inhibited FGF-2-stimulated proliferation of HPASMC incubated in either 5% or 20% O-2 but failed to inhibit the comitogenic effect of hypoxia. Knockdown of HIF-1 alpha similarly inhibited PDGF-stimulated proliferation, whereas HIF-2 alpha knockdown had no effect on HPASMC proliferation. Knockdown of HIF-1 alpha expression also inhibited growth factor-induced expression of cyclin A. We conclude that HIF-1 alpha promotes proliferative responses of human VSMC to FGF-2, PDGF, and EGF by mechanisms that may involve HIF-1-dependent expression of cyclin A, but HIF is apparently not crucial to the enhancement of FGF-2-, PDGF-, and EGF-induced proliferation of VSMC that occurs during hypoxia.
