Referenced in: none

Automatically associated channels: TRP , TRPC , TRPC6

Title: Crucial role of TRPC6 in maintaining the stability of HIF-1α in glioma cells under hypoxia.

Authors: Shanshan Li, Jinkui Wang, Yi Wei, Yongjian Liu, Xia Ding, Bin Dong, Yinghui Xu, Yizheng Wang

Journal, date & volume: J. Cell. Sci., 2015 Sep 1 , 128, 3317-29

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26187851

Abstract
Hypoxia-inducible factor-1 (HIF-1) is a key transcription factor responsible for the expression of a broad range of genes that facilitate acclimatization to hypoxia. Its stability is predominantly controlled by rapid hydroxylation of two proline residues in its α-subunit. However, how the rapid hydroxylation of HIF-1α is regulated is not fully understood. Here, we report that transient receptor potential canonical (TRPC) 6 channels control hydroxylation and stability of HIF-1α in human glioma cells under hypoxia. TRPC6 was rapidly activated by IGF-1R-PLCγ-IP3R pathway upon hypoxia. Inhibition of TRPC6 enhanced the levels of α-ketoglutarate and promoted hydroxylation of HIF-1α to suppress HIF-1α accumulation without affecting its transcription or translation. Dimethyloxalylglycine N-(methoxyoxoacetyl)-glycine methyl ester (DMOG), an analog of α-ketoglutarate, reversed the inhibition of HIF-1α accumulation. Moreover, TRPC6 regulated GLUT1 (also known as SLC2A1) expression in a manner that was dependent on HIF-1α accumulation to affect glucose uptake during hypoxia. Our results suggest that TRPC6 regulates metabolism to affect HIF-1α stability and consequent glucose metabolism in human glioma cells under hypoxia.