The murine choroid plexus epithelium expresses the 2Cl -/H + exchanger ClC-7 and Na +/H + exchanger NHE6 in the luminal membrane domain

Am J Physiol Cell Physiol. 2018 Apr 1;314(4):C439-C448. doi: 10.1152/ajpcell.00145.2017. Epub 2017 Dec 20.

Abstract

The choroid plexus epithelium within the brain ventricles secretes the majority of the cerebrospinal fluid (CSF). The luminal Na+-K+-ATPase acts in concert with a host of other transport proteins to mediate efficient fluid secretion across the epithelium. The CSF contains little protein buffer, but the pH value seems nonetheless maintained within narrow limits, even when faced with acid-base challenges. The involvement of choroid plexus acid-base transporters in CSF pH regulation is highlighted by the expression of several acid-base transporters in the epithelium. The aim of the present study was to identify novel acid-base transporters expressed in the luminal membrane of the choroid plexus epithelium to pave the way for systematic investigations of each candidate transporter in the regulation of CSF pH. Mass spectrometry analysis of proteins from epithelial cells isolated by fluorescence-activated cell sorting identified the Cl-/H+ exchangers ClC-3, -4, -5, and -7 in addition to known choroid plexus acid-base transporters. RT-PCR on FACS isolated epithelial cells confirmed the expression of the corresponding mRNAs, as well as Na+/H+ exchanger NHE6 mRNA. Both NHE6 and ClC-7 were immunolocalized to the luminal plasma membrane domain of the choroid plexus epithelial cells. Dynamic imaging of intracellular pH and membrane potential changes in isolated choroid plexus epithelial cells demonstrated Cl- gradient-driven changes in intracellular pH and membrane potential that are consistent with Cl-/H+ exchange. In conclusion, we have detected for the first time NHE6 and ClC-7 in the choroid plexus, which are potentially involved in pH regulation of the CSF.

Keywords: acid-base transport; cerebrospinal fluid; choroid plexus; intracellular pH; mass spectrometry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane / metabolism*
  • Cell Separation / methods
  • Cerebrospinal Fluid / metabolism*
  • Chloride Channels / genetics
  • Chloride Channels / metabolism*
  • Choroid Plexus / cytology
  • Choroid Plexus / metabolism*
  • Epithelial Cells / metabolism*
  • Flow Cytometry
  • Hydrogen-Ion Concentration
  • Male
  • Membrane Potentials
  • Mice, Inbred C57BL
  • Proteomics / methods
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / metabolism*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Chloride Channels
  • Clcn7 protein, mouse
  • NHE6 protein, mouse
  • Sodium-Hydrogen Exchangers