Arterial smooth muscle cell PKD2 (TRPP1) channels regulate systemic blood pressure

Author:

Bulley Simon1ORCID,Fernández-Peña Carlos1ORCID,Hasan Raquibul1,Leo M Dennis1,Muralidharan Padmapriya1,Mackay Charles E1,Evanson Kirk W1,Moreira-Junior Luiz1,Mata-Daboin Alejandro1,Burris Sarah K1,Wang Qian1,Kuruvilla Korah P1,Jaggar Jonathan H1ORCID

Affiliation:

1. Department of Physiology, University of Tennessee Health Science Center, Memphis, United States

Abstract

Systemic blood pressure is determined, in part, by arterial smooth muscle cells (myocytes). Several Transient Receptor Potential (TRP) channels are proposed to be expressed in arterial myocytes, but it is unclear if these proteins control physiological blood pressure and contribute to hypertension in vivo. We generated the first inducible, smooth muscle-specific knockout mice for a TRP channel, namely for PKD2 (TRPP1), to investigate arterial myocyte and blood pressure regulation by this protein. Using this model, we show that intravascular pressure and α1-adrenoceptors activate PKD2 channels in arterial myocytes of different systemic organs. PKD2 channel activation in arterial myocytes leads to an inward Na+ current, membrane depolarization and vasoconstriction. Inducible, smooth muscle cell-specific PKD2 knockout lowers both physiological blood pressure and hypertension and prevents pathological arterial remodeling during hypertension. Thus, arterial myocyte PKD2 controls systemic blood pressure and targeting this TRP channel reduces high blood pressure.

Funder

American Heart Association

National Heart, Lung, and Blood Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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