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

Am J Physiol Heart Circ Physiol. 2008 Apr;294(4):H1700-7. doi: 10.1152/ajpheart.01203.2007. Epub 2008 Feb 8.

Abstract

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 Ca(2+), an essential signal of cell growth, is still not known. The aim of the present study was to elucidate the role of NHE1 in Ca(2+) signaling and the proliferation of human CNS pericytes. The intracellular Ca(2+) concentration was measured by fura 2 in cultured human CNS pericytes. The cells showed spontaneous Ca(2+) oscillation under quasi-physiological ionic conditions. A decrease in extracellular pH or Na(+) evoked a transient Ca(2+) rise followed by Ca(2+) oscillation, whereas an increase in pH or Na(+) did not induce the Ca(2+) responses. The Ca(2+) oscillation was inhibited by an inhibitor of NHE in a dose-dependent manner and by knockdown of NHE1 by using RNA interference. The Ca(2+) oscillation was completely abolished by thapsigargin. The proliferation of pericytes was attenuated by inhibition of NHE1. These results demonstrate that NHE1 regulates Ca(2+) signaling via the modulation of Ca(2+) release from the endoplasmic reticulum, thus contributing to the regulation of proliferation in CNS pericytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amiloride / analogs & derivatives
  • Amiloride / pharmacology
  • Brain / blood supply*
  • Calcium / metabolism
  • Calcium Signaling* / drug effects
  • Cation Transport Proteins / antagonists & inhibitors
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism*
  • Cell Proliferation* / drug effects
  • Cells, Cultured
  • Endoplasmic Reticulum / metabolism
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Hydrogen-Ion Concentration
  • Microcirculation / metabolism
  • Pericytes / drug effects
  • Pericytes / enzymology
  • Pericytes / metabolism*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / antagonists & inhibitors
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism
  • Sodium / metabolism
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers / antagonists & inhibitors
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / metabolism*
  • Thapsigargin / pharmacology
  • Time Factors

Substances

  • Cation Transport Proteins
  • Enzyme Inhibitors
  • RNA, Small Interfering
  • SLC9A1 protein, human
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers
  • benzamil
  • 5-(N,N-hexamethylene)amiloride
  • Thapsigargin
  • Amiloride
  • Sodium
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases
  • Calcium