Inward-rectifying anion channels are expressed in the epithelial cells of choroid plexus isolated from ClC-2 ‘knock-out’ mice

• Published in: The Journal of physiology Vol. 539; no. 2; p. 385
• Main Authors: Tracey Speake, Hidetoshi Kajita, Craig P Smith, Peter D Brown
• Format: Journal Article
• Language: English
• Published: The Physiological Society 01.03.2002
• ISSN: 0022-3751; 1469-7793
• DOI: 10.1113/jphysiol.2001.014548

Choroid plexus epithelial cells express inward-rectifying anion channels which have a high HCO 3 − permeability. These channels are thought to have an important role in the secretion of cerebrospinal fluid. The possible relationship between these channels and the ClC-2 Cl − channel was investigated in the present study. RT-PCR, using specific ClC-2 primers, amplified a 238 bp fragment of mRNA from rat choroid plexus, which was 99 % identical to the 5′ sequence of rat ClC-2. A 2005 bp clone was isolated from a rat choroid plexus cDNA library using a probe for ClC-2. The clone showed greater than 99 % identity with the sequence of rat ClC-2. Inward-rectifying anion channels were observed in whole-cell recordings of choroid plexus epithelial cells isolated from ClC-2 knock-out mice. The mean inward conductance was 19.6 ± 3.6 nS ( n = 8) in controls (3 heterozygote animals), and 22.5 ± 3.1 nS ( n = 10) in three knock-out animals. The relative permeability of the conductances to I − and Cl − ( P I : P Cl ) was determined. I − was more permeant than Cl − in both heterozygotes ( P I : P Cl = 4.0 ± 0.9, n = 3) and knock-out animals ( P I : P Cl = 4.1 ± 1.4, n = 3). These results indicate that rat choroid plexus expresses the ClC-2 variant that was originally reported in other tissues. ClC-2 does not contribute significantly to inward-rectifying anion conductance in mouse choroid plexus, which must therefore express a novel inward-rectifying anion channel.