ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion

Mutations in the 2Cl-/1H+-exchanger ClC-7 impair osteoclast function and cause different types of osteoclast-rich osteopetrosis. However, it is unknown to what extent ClC-7 function has to be reduced to become rate-limiting for bone resorption. In osteoclasts from osteopetrosis patients expression o...

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Main Authors: Supanchart C., Wartosch L., Schlack C., Kuhnisch J., Felsenberg D., Fuhrmann J.C., de Vernejoul M.-C., Jentsch T.J., Kornak U.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84886859886&partnerID=40&md5=75744fda9332ed7c9e63c982dd63d06d
http://cmuir.cmu.ac.th/handle/6653943832/1179
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spelling th-cmuir.6653943832-11792014-08-29T09:17:50Z ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion Supanchart C. Wartosch L. Schlack C. Kuhnisch J. Felsenberg D. Fuhrmann J.C. de Vernejoul M.-C. Jentsch T.J. Kornak U. Mutations in the 2Cl-/1H+-exchanger ClC-7 impair osteoclast function and cause different types of osteoclast-rich osteopetrosis. However, it is unknown to what extent ClC-7 function has to be reduced to become rate-limiting for bone resorption. In osteoclasts from osteopetrosis patients expression of the mutated ClC-7 protein did not correlate with disease severity and resorption impairment. Therefore, a series of transgenic mice expressing ClC-7 in osteoclasts at different levels was generated. Crossing of these mice with Clcn7-/- mutants rescued the osteopetrotic phenotype to variable degrees. One resulting double transgenic line mimicked human autosomal dominant osteopetrosis. The trabecular bone of these mice showed a reduction of osteoblast numbers, osteoid, and osteoblast marker gene expression indicative of reduced osteoblast function. In osteoclasts from these mutants ClC-7 expression levels were 20 to 30% of wildtype levels. These reduced levels not only impaired resorptive activity, but also increased numbers, size and nucleus numbers of osteoclasts differentiated in vitro. Although ClC-7 was expressed in the stomach and PTH levels were high in Clcn7-/- mutants loss of ClC-7 did not entail a relevant elevation of gastric pH. In conclusion, we show that in our model a reduction of ClC-7 function by approximately 70% is sufficient to increase bone mass, but does not necessarily enhance bone formation. ClC-7 does not appear to be crucially involved in gastric acid secretion, which explains the absence of an osteopetrorickets phenotype in CLCN7-related osteopetrosis. © 2013 Elsevier Inc. 2014-08-29T09:17:50Z 2014-08-29T09:17:50Z 2014 Article 87563282 10.1016/j.bone.2013.09.022 BONED http://www.scopus.com/inward/record.url?eid=2-s2.0-84886859886&partnerID=40&md5=75744fda9332ed7c9e63c982dd63d06d http://cmuir.cmu.ac.th/handle/6653943832/1179 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
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language English
description Mutations in the 2Cl-/1H+-exchanger ClC-7 impair osteoclast function and cause different types of osteoclast-rich osteopetrosis. However, it is unknown to what extent ClC-7 function has to be reduced to become rate-limiting for bone resorption. In osteoclasts from osteopetrosis patients expression of the mutated ClC-7 protein did not correlate with disease severity and resorption impairment. Therefore, a series of transgenic mice expressing ClC-7 in osteoclasts at different levels was generated. Crossing of these mice with Clcn7-/- mutants rescued the osteopetrotic phenotype to variable degrees. One resulting double transgenic line mimicked human autosomal dominant osteopetrosis. The trabecular bone of these mice showed a reduction of osteoblast numbers, osteoid, and osteoblast marker gene expression indicative of reduced osteoblast function. In osteoclasts from these mutants ClC-7 expression levels were 20 to 30% of wildtype levels. These reduced levels not only impaired resorptive activity, but also increased numbers, size and nucleus numbers of osteoclasts differentiated in vitro. Although ClC-7 was expressed in the stomach and PTH levels were high in Clcn7-/- mutants loss of ClC-7 did not entail a relevant elevation of gastric pH. In conclusion, we show that in our model a reduction of ClC-7 function by approximately 70% is sufficient to increase bone mass, but does not necessarily enhance bone formation. ClC-7 does not appear to be crucially involved in gastric acid secretion, which explains the absence of an osteopetrorickets phenotype in CLCN7-related osteopetrosis. © 2013 Elsevier Inc.
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author Supanchart C.
Wartosch L.
Schlack C.
Kuhnisch J.
Felsenberg D.
Fuhrmann J.C.
de Vernejoul M.-C.
Jentsch T.J.
Kornak U.
spellingShingle Supanchart C.
Wartosch L.
Schlack C.
Kuhnisch J.
Felsenberg D.
Fuhrmann J.C.
de Vernejoul M.-C.
Jentsch T.J.
Kornak U.
ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
author_facet Supanchart C.
Wartosch L.
Schlack C.
Kuhnisch J.
Felsenberg D.
Fuhrmann J.C.
de Vernejoul M.-C.
Jentsch T.J.
Kornak U.
author_sort Supanchart C.
title ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
title_short ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
title_full ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
title_fullStr ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
title_full_unstemmed ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion
title_sort clc-7 expression levels critically regulate bone turnover, but not gastric acid secretion
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84886859886&partnerID=40&md5=75744fda9332ed7c9e63c982dd63d06d
http://cmuir.cmu.ac.th/handle/6653943832/1179
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