Abstract
CLC-7 is a member of the voltage-gated chloride channels family. It resides mainly in the late endosomes, lysosomes and the ruffled membrane of osteoclasts. Mice deficient in the ubiquitously expressed ClC-7 Cl(-) channel show severe osteopetrosis and retinal degeneration. In the present review, some of the known features of CLC-7 such as structure, function and its roles in physiological or pathophysiological processes are highlighted.
MeSH terms
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Animals
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Chloride Channels / antagonists & inhibitors*
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Chloride Channels / genetics
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Chloride Channels / metabolism*
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Humans
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Mice
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Neurodegenerative Diseases / drug therapy*
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Neurodegenerative Diseases / genetics
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Neurodegenerative Diseases / metabolism
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Osteopetrosis / drug therapy*
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Osteopetrosis / genetics
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Osteopetrosis / metabolism
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Retinal Degeneration / drug therapy*
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Retinal Degeneration / genetics
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Retinal Degeneration / metabolism
Substances
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CLCN7 protein, human
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Chloride Channels