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Role of NHE1 in calcium signaling and cell proliferation in human CNS pericytes

¹Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, and ²Department of Medicine, Seiai Rehabilitation Hospital and Fukuoka Institute of Neurogenetics and Stroke, Fukuoka, Japan

Submitted 17 October 2007 ; accepted in final form 6 February 2008

The central nervous system (CNS) pericytes play an important role in brain microcirculation. Na⁺/H⁺ exchanger isoform 1 (NHE1) has been suggested to regulate the proliferation of nonvascular cells through the regulation of intracellular pH, Na⁺, and cell volume; however, the relationship between NHE1 and intracellular Ca²⁺, an essential signal of cell growth, is still not known. The aim of the present study was to elucidate the role of NHE1 in Ca²⁺ signaling and the proliferation of human CNS pericytes. The intracellular Ca²⁺ concentration was measured by fura 2 in cultured human CNS pericytes. The cells showed spontaneous Ca²⁺ oscillation under quasi-physiological ionic conditions. A decrease in extracellular pH or Na⁺ evoked a transient Ca²⁺ rise followed by Ca²⁺ oscillation, whereas an increase in pH or Na⁺ did not induce the Ca²⁺ responses. The Ca²⁺ oscillation was inhibited by an inhibitor of NHE in a dose-dependent manner and by knockdown of NHE1 by using RNA interference. The Ca²⁺ oscillation was completely abolished by thapsigargin. The proliferation of pericytes was attenuated by inhibition of NHE1. These results demonstrate that NHE1 regulates Ca²⁺ signaling via the modulation of Ca²⁺ release from the endoplasmic reticulum, thus contributing to the regulation of proliferation in CNS pericytes.

Na⁺/H⁺ exchanger; central nervous system; cerebral ischemia; microcirculation