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Hypoxia and hypoxia-inducible factor-1 promote growth factor-induced proliferation of human vascular smooth muscle cells

¹Molecular Cardiology Research Institute and ²Pulmonary, Critical Care, and Sleep Division, Department of Medicine, Tufts-New England Medical Center, and Tufts University School of Medicine, Boston, Massachusetts

Submitted 12 October 2005 ; accepted in final form 22 December 2005

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- (HIF-1), 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% O₂) 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% O₂). Moderate hypoxia elicited increased cellular HIF-1 levels, shown by Western blot analysis, and also enhanced PDGF-, FGF-2-, and EGF-induced expression of HIF-1. Knockdown of HIF-1 or HIF-1 levels in HPASMC with specific small interfering RNAs inhibited FGF-2-stimulated proliferation of HPASMC incubated in either 5% or 20% O₂ but failed to inhibit the comitogenic effect of hypoxia. Knockdown of HIF-1 similarly inhibited PDGF-stimulated proliferation, whereas HIF-2 knockdown had no effect on HPASMC proliferation. Knockdown of HIF-1 expression also inhibited growth factor-induced expression of cyclin A. We conclude that HIF-1 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.

platelet-derived growth factor; fibroblast growth factor; cyclin A; oxygen

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