Hypoxia-Inducible Factor-1α Expression in Macrophages Promotes Development of Atherosclerosis

OBJECTIVE—Atherosclerotic lesions contain hypoxic areas, but the pathophysiological importance of hypoxia is unknown. Hypoxia-inducible factor-1α (HIF-1α) is a key transcription factor in cellular responses to hypoxia. We investigated the hypothesis that HIF-1α has effects on macrophage biology that...

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Published inArteriosclerosis, thrombosis, and vascular biology Vol. 36; no. 9; pp. 1782 - 1790
Main Authors Aarup, Annemarie, Pedersen, Tanja X, Junker, Nanna, Christoffersen, Christina, Bartels, Emil D, Madsen, Marie, Nielsen, Carsten H, Nielsen, Lars B
Format Journal Article
LanguageEnglish
Published United States American Heart Association, Inc 01.09.2016
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Summary:OBJECTIVE—Atherosclerotic lesions contain hypoxic areas, but the pathophysiological importance of hypoxia is unknown. Hypoxia-inducible factor-1α (HIF-1α) is a key transcription factor in cellular responses to hypoxia. We investigated the hypothesis that HIF-1α has effects on macrophage biology that promotes atherogenesis in mice. APPROACH AND RESULTS—Studies with molecular probes, immunostaining, and laser microdissection of aortas revealed abundant hypoxic, HIF-1α–expressing macrophages in murine atherosclerotic lesions. To investigate the significance of macrophage HIF-1α, Ldlr mice were transplanted with bone marrow from mice with HIF-1α deficiency in the myeloid cells or control bone marrow. The HIF-1α deficiency in myeloid cells reduced atherosclerosis in aorta of the Ldlr recipient mice by ≈72% (P=0.006).In vitro, HIF-1α–deficient macrophages displayed decreased differentiation to proinflammatory M1 macrophages and reduced expression of inflammatory genes. HIF-1α deficiency also affected glucose uptake, apoptosis, and migratory abilities of the macrophages. CONCLUSIONS—HIF-1α expression in macrophages affects their intrinsic inflammatory profile and promotes development of atherosclerosis.
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ISSN:1079-5642
1524-4636
DOI:10.1161/ATVBAHA.116.307830