Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:Q9UIJ5 (
Rec
)
58,342
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
ClC-7
is a 2Cl(-) /1H(+) -exchanger expressed at late endosomes and lysosomes, as well as the ruffled border of osteoclasts.
ClC-7
deficiencies in mice and humans lead to impaired osteoclast function and therefore osteopetrosis. Failure of tooth eruption is also apparent in
ClC-7
mutant animals, and this has been attributed to the osteoclast dysfunction and the subsequent defect in alveolar bone resorptive activity surrounding tooth roots. Ameloblasts also express
ClC-7
, and this study aims to determine the significance of
ClC-7
in enamel formation by examining the dentitions of
ClC-7
mutant mice. Micro-CT analysis revealed that the molar teeth of 3-week old
ClC-7
mutant mice had no roots, and the incisors were smaller than their age-matched controls. Despite these notable developmental differences, the enamel and dentin densities of the mutant mice were comparable to those of the wild-type littermates. Scanning electron microscopy showed normal enamel crystallite and prismatic organization in the
ClC-7
mutant mice, although the enamel was thinner (hypoplastic) than in controls. These results suggested that
ClC-7
was not critical to enamel and dentin formation, and the observed tooth defects may be related more to a resulting alveolar bone phenotype. Micro-CT analysis also revealed abnormal features in the calvarial bones of the mutant mice. The cranial sutures in
ClC-7
mutant mice remained open compared to the closed sutures seen in the control mice at 3 weeks. These data demonstrate that
ClC-7
deficiency impacts the development of the dentition and calvaria, but does not significantly disrupt amelogenesis.
Anat
Rec
(Hoboken) 2015 Aug
PMID:Dental and Cranial Pathologies in Mice Lacking the Cl(-) /H(+) -Exchanger ClC-7. 2566 54