WNK kinase is a vasoactive chloride sensor in endothelial cells.

Abstract

Endothelial cells (ECs) line the wall of blood vessels and regulate arterial contractility to tune regional organ blood flow and systemic pressure. Chloride (Cl^-) is the most abundant anion in ECs and the Cl^- sensitive With-No-Lysine (WNK) kinase is expressed in this cell type. Whether intracellular Cl^- signaling and WNK kinase regulate EC function to alter arterial contractility is unclear. Here, we tested the hypothesis that intracellular Cl^- signaling in ECs regulates arterial contractility and examined the signaling mechanisms involved, including the participation of WNK kinase. Our data obtained using two-photon microscopy and cell-specific inducible knockout mice indicated that acetylcholine, a prototypical vasodilator, stimulated a rapid reduction in intracellular Cl^- concentration ([Cl^-]_i) due to the activation of TMEM16A, a Cl^- channel, in ECs of resistance-size arteries. TMEM16A channel-mediated Cl^- signaling activated WNK kinase, which phosphorylated its substrate proteins SPAK and OSR1 in ECs. OSR1 potentiated transient receptor potential vanilloid 4 (TRPV4) currents in a kinase-dependent manner and required a conserved binding motif located in the channel C terminus. Intracellular Ca²⁺ signaling was measured in four dimensions in ECs using a high-speed lightsheet microscope. WNK kinase-dependent activation of TRPV4 channels increased local intracellular Ca²⁺ signaling in ECs and produced vasodilation. In summary, we show that TMEM16A channel activation reduces [Cl^-]_i, which activates WNK kinase in ECs. WNK kinase phosphorylates OSR1 which then stimulates TRPV4 channels to produce vasodilation. Thus, TMEM16A channels regulate intracellular Cl^- signaling and WNK kinase activity in ECs to control arterial contractility.