Key result
HIF critically regulates hypoxia-induced vascular and pulmonary arterial remodeling.
Why the study?
Hypoxia-inducible factor (HIF) is a crucial regulator of hypoxia-induced vascular remodeling, but the detailed cellular and molecular mechanisms remain to be summarized and discussed.
This review highlights the crucial role of hypoxia-inducible factor (HIF) in driving various forms of vascular remodeling, including adaptive angiogenesis and pathological pulmonary arterial remodeling.
Hypoxia-inducible factor (HIF) is an oxygen-dependent transcription factor that activates a diverse set of target genes, the products of which are involved in adaptive processes to hypoxia. Employing genetic manipulation of HIF expression, in-vivo and cellular studies have focused on HIF as a crucial factor affecting hypoxia-induced vascular remodeling. Vascular remodeling comprises processes which establish and improve blood vessel supply such as vasculogenesis, angiogenesis and arteriogenesis. These processes are observed during ontogenesis, tumor progression, ischemic disease or physical training. Furthermore, under hypoxic conditions, a pulmonary-specific type of vascular remodeling called pulmonary arterial remodeling occurs that is characterized by thickening of the vessel wall with a concomitant reduction in the vessel lumen area, thereby limiting blood flow. This response results in pulmonary hypertension with right ventricular hypertrophy, a lethal disease. In this review, we summarize and discuss mechanisms by which HIF interferes with the different vascular remodeling processes.
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Weißmann et al. (2007) conducted a review in Hypoxia-induced vascular remodeling. Hypoxia-inducible factor (HIF) was evaluated. Hypoxia-inducible factor (HIF) acts as a crucial factor affecting hypoxia-induced vascular remodeling, including vasculogenesis, angiogenesis, arteriogenesis, and pulmonary arterial remodeling.
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