Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man

Citation
U. Kornak et al., Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man, CELL, 104(2), 2001, pp. 205-215
Citations number
40
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELL
ISSN journal
00928674 → ACNP
Volume
104
Issue
2
Year of publication
2001
Pages
205 - 215
Database
ISI
SICI code
0092-8674(20010126)104:2<205:LOTCCC>2.0.ZU;2-C
Abstract
Chloride channels play important roles in the plasma membrane and in intrac ellular organelles. Mice deficient for the ubiquitously expressed CIC-7 Cl- channel show severe osteopetrosis and retinal degeneration. Although osteo clasts are present in normal numbers, they fail to resorb bone because they cannot acidify the extracellular resorption lacuna. CIC-7 resides in late endosomal and lysosomal compartments. In osteoclasts, it is highly expresse d in the ruffled membrane, formed by the fusion of H+-ATPase-containing ves icles, that secretes protons into the lacuna. We also identified CLCN7 muta tions in a patient with human Infantile malignant osteopetrosis. We conclud e that CIC-7 provides the chloride conductance required for an efficient pr oton pumping by the H+-ATPase of the osteoclast ruffled membrane.