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Smooth Muscle Hypoxia-Inducible Factor 1α Links Intravascular Pressure and Atherosclerosis—Brief Report
Author(s) -
Dinggang Liu,
Lei Li,
Matthew Desir,
Yan Huang,
Jacob Cleman,
Weidong Jiang,
Carlos FernándezHernando,
Annarita Di Lorenzo,
William C. Sessa,
Frank J. Giordano
Publication year - 2016
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.115.306861
Subject(s) - vascular smooth muscle , inflammation , apolipoprotein e , hypoxia (environmental) , medicine , pathogenesis , cardiology , blood pressure , constriction , pathology , endocrinology , smooth muscle , chemistry , oxygen , disease , organic chemistry
Objective— We hypothesized that the hypoxia-inducible factor (HIF) 1α in vascular smooth muscle contributes to the development of atherosclerosis, and links intravascular pressure to this process. Approach and Results— Transverse aortic constriction was used to create high-pressure vascular segments in control, apolipoprotein E (ApoE )−/− , smooth muscle-HIF1α−/− , andApoE−/− ×smooth muscle-HIF1α−/− double-knockout mice. Transverse aortic constriction selectively induced atherosclerosis in high-pressure vascular segments in youngApoE−/− mice on normal chow, including coronary plaques within 1 month. Concomitant deletion ofHIF1α from smooth muscle significantly reduced vascular inflammation, and attenuated atherosclerosis.Conclusions— HIF1α in vascular smooth muscle plays an important role in the pathogenesis of atherosclerosis, and may provide a mechanistic link between blood pressure, vascular inflammation, and lipid deposition.

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