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.