2015 Fiscal Year Final Research Report
Molecular physiological studies on functional differences among isoforms of ClC-3
Project/Area Number |
24590291
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General physiology
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Research Institution | National Institute for Physiological Sciences |
Principal Investigator |
Okada Toshiaki 生理学研究所, 細胞器官研究系, 特任准教授 (00373283)
|
Project Period (FY) |
2012-04-01 – 2016-03-31
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Keywords | イオンチャネル / 電気生理 / 分子クローニング |
Outline of Final Research Achievements |
ClC-3, a member of the Cl-channel/transpoter family, is predicted to have six isoforms, ClC-3a to -3f, with distinct N- and C-terminal amino acid sequences, however amino acid sequences of ClC-3d was derived from genomic sequence, but there was no experimental evidence for mRNAs. We recently cloned a cDNA containing the full coding region of ClC-3d. In this study, we analyzed the channel properties of ClC-3d by whole-cell patch-clamp recordings and identified basic properties of this channel. We identified that ClC-3d, like ClC- 3a, mediates Cd2+-sensitive outwardly rectifying anion currents and that ClC-3d is distinct from the molecular entities of acid- and volume-sensitive anion channels. Electrophysiological properties of ClC-3 have long been investigated but are still unclear. Our results may help elucidate them.
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Free Research Field |
生理学
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