Referenced in: none

Automatically associated channels: TRP , TRPC , TRPC3

Title: Increased migration of monocytes in essential hypertension is associated with increased transient receptor potential channel canonical type 3 channels.

Authors: Zhigang Zhao, Yinxing Ni, Jing Chen, Jian Zhong, Hao Yu, Xingsen Xu, Hongbo He, Zhencheng Yan, Alexandra Scholze, Daoyan Liu, Zhiming Zhu, Martin Tepel

Journal, date & volume: PLoS ONE, 2012 , 7, e32628

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22438881

Abstract
Increased transient receptor potential canonical type 3 (TRPC3) channels have been observed in patients with essential hypertension. In the present study we tested the hypothesis that increased monocyte migration is associated with increased TRPC3 expression. Monocyte migration assay was performed in a microchemotaxis chamber using chemoattractants formylated peptide Met-Leu-Phe (fMLP) and tumor necrosis factor-α (TNF-α). Proteins were identified by immunoblotting and quantitative in-cell Western assay. The effects of TRP channel-inhibitor 2-aminoethoxydiphenylborane (2-APB) and small interfering RNA knockdown of TRPC3 were investigated. We observed an increased fMLP-induced migration of monocytes from hypertensive patients compared with normotensive control subjects (246 ± 14% vs 151 ± 10%). The TNF-α-induced migration of monocytes in patients with essential hypertension was also significantly increased compared to normotensive control subjects (221 ± 20% vs 138 ± 18%). In the presence of 2-APB or after siRNA knockdown of TRPC3 the fMLP-induced monocyte migration was significantly blocked. The fMLP-induced changes of cytosolic calcium were significantly increased in monocytes from hypertensive patients compared to normotensive control subjects. The fMLP-induced monocyte migration was significantly reduced in the presence of inhibitors of tyrosine kinase and phosphoinositide 3-kinase. We conclude that increased monocyte migration in patients with essential hypertension is associated with increased TRPC3 channels.