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bioRxiv · 10.1101/2024.05.29.595538

Branched chain α-ketoacids aerobically activate HIF1α signaling in vascular cells

Abstract

Hypoxia-inducible factor 1 (HIF1) is a master regulator of numerous biological processes under low oxygen tensions. Yet, the mechanisms and biological consequences of aerobic HIF1 activation by intrinsic factors, particularly in primary cells remain elusive. Here, we show that HIF1 signaling is activated in several human primary vascular cells under ambient oxygen tensions, and in vascular smooth muscle cells (VSMCs) of normal human lung tissue, which contributed to a relative resistance to further enhancement of glycolytic activity in hypoxia. Mechanistically, aerobic HIF activation is mediated by paracrine secretion of three branched chain -ketoacids (BCKAs), which suppress prolyl hydroxylase domain-containing protein 2 (PHD2) activity via direct inhibition and via lactate dehydrogenase A (LDHA)-mediated generation of L-2-hydroxyglutarate (L2HG). Metabolic dysfunction induced by BCKAs was observed in the lungs of rats with pulmonary arterial hypertension (PAH) and in pulmonary artery smooth muscle cells (PASMCs) from idiopathic PAH patients. BCKA supplementation stimulated glycolytic activity and promoted a phenotypic switch to the synthetic phenotype in PASMCs of normal and PAH subjects. In summary, we identify BCKAs as novel signaling metabolites that activate HIF1 signaling in normoxia and that the BCKA-HIF1 pathway modulates VSMC function and may be relevant to pulmonary vascular pathobiology.

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BibTeXRIS

Loscalzo, J., Xiao, W., Shrimali, N., Oldham, W. M., Clish, C. B., He, H., Wong, S. J., Wertheim, B. M., Arons, E., Haigis, M. C., Leopold, J. A.. 2024-05-30. Branched chain α-ketoacids aerobically activate HIF1α signaling in vascular cells. https://doi.org/10.1101/2024.05.29.595538

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