Kasper, D. et al. Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration. EMBO J. 24, 1079−1091

Zentrum für Molekulare Neurobiologie,Universität Hamburg, Hamburg, Germany.
The EMBO Journal (Impact Factor: 10.43). 04/2005; 24(5):1079-91. DOI: 10.1038/sj.emboj.7600576
Source: PubMed


ClC-7 is a chloride channel of late endosomes and lysosomes. In osteoclasts, it may cooperate with H(+)-ATPases in acidifying the resorption lacuna. In mice and man, loss of ClC-7 or the H(+)-ATPase a3 subunit causes osteopetrosis, a disease characterized by defective bone resorption. We show that ClC-7 knockout mice additionally display neurodegeneration and severe lysosomal storage disease despite unchanged lysosomal pH in cultured neurons. Rescuing their bone phenotype by transgenic expression of ClC-7 in osteoclasts moderately increased their lifespan and revealed a further progression of the central nervous system pathology. Histological analysis demonstrated an accumulation of electron-dense material in neurons, autofluorescent structures, microglial activation and astrogliosis. Like in human neuronal ceroid lipofuscinosis, there was a strong accumulation of subunit c of the mitochondrial ATP synthase and increased amounts of lysosomal enzymes. Such alterations were minor or absent in ClC-3 knockout mice, despite a massive neurodegeneration. Osteopetrotic oc/oc mice, lacking a functional H(+)-ATPase a3 subunit, showed no comparable retinal or neuronal degeneration. There are important medical implications as defects in the H(+)-ATPase and ClC-7 can underlie human osteopetrosis.

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    • "Disruption of the Clcn7 gene in mice results in severe osteopetrosis in the long bones of the extremities, shorter stature and splenomegaly (Kornak et al. 2001). Failure of teeth to erupt has also been reported for Clcn7 -/-mice but the description was not very detailed (Kasper et al. 2005; Kornak et al. 2001; Wen et al. 2015). Ameloblasts secrete proteases as MMP20 and KLK4 to degrade most of the enamel matrix followed by endocytosis and digestion of at least a portion of the peptide fragments , particularly during maturation stage. "
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    ABSTRACT: ClC-7, located in late endosomes and lysosomes, is critical for the function of osteoclasts. Secretion of Cl(-) by the ruffled border of osteoclasts enables H(+) secretion by v-H(+)-ATPases to dissolve bone mineral. Mice lacking ClC-7 show altered lysosomal function that leads to severe lysosomal storage. Maturation ameloblasts are epithelial cells with a ruffled border that secrete Cl(-) as well as endocytose and digest large quantities of enamel matrix proteins during formation of dental enamel. We tested the hypothesis that ClC-7 in maturation ameloblasts is required for intracellular digestion of matrix fragments to complete enamel mineralization. Craniofacial bones and developing teeth in Clcn7 (-/-) mice were examined by micro-CT, immunohistochemistry, quantified histomorphometry and electron microscopy. Osteoclasts and ameloblasts in wild-type mice stained intensely with anti-ClC-7 antibody but not in Clcn7 (-/-) mice. Craniofacial bones in Clcn7 (-/-) mice were severely osteopetrotic and contained 1.4- to 1.6-fold more bone volume, which was less mineralized than the wild-type littermates. In Clcn7 (-/-) mice maturation ameloblasts and osteoclasts highly expressed Ae2 as in wild-type mice. However, teeth failed to erupt, incisors were much shorter and roots were disfigured. Molars formed a normal dental crown. In compacted teeth, dentin was slightly less mineralized, enamel did not retain a matrix and mineralized fairly normal. We concluded that ClC-7 is essential for osteoclasts to resorb craniofacial bones to enable tooth eruption and root development. Disruption of Clcn7 reduces bone and dentin mineral density but does not affect enamel mineralization.
    Cell and Tissue Research 09/2015; DOI:10.1007/s00441-015-2263-z · 3.57 Impact Factor
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    • "gl mice suffer from anaemia, leucopoenia, and lymphopoenia, and furthermore develop a reduced thymus (Pata et al. 2008). Although the osteopetrotic phenotype caused by the loss of ClC-7 can be rescued by transgenic expression of ClC-7 in osteoclasts (Kasper et al. 2005), the phenotype of gl "
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    ABSTRACT: The CLC family of chloride channels and transporters is composed by nine members, but only three of them, ClC-Ka/b, ClC-7 and ClC-2, have been found so far associated with auxiliary subunits. These CLC regulatory subunits are small proteins that present few common characteristics among them, both structurally and functionally, and their effects on the corresponding CLC protein are different. Barttin, a protein with two transmembrane domains, is essential for the membrane localization of ClC-K proteins and their activity in the kidney and inner ear. Ostm1 is a protein with a single transmembrane domain and a highly glycosylated N-terminus. Unlike the other two CLC auxiliary subunits, Ostm1 shows a reciprocal relationship with ClC-7 for their stability. The subcellular localization of Ostm1 depends on ClC-7 and not the other way around. ClC-2 is active on its own, but GlialCAM, a transmembrane cell adhesion molecule with two extracellular Ig-like domains, regulates its subcellular localization and activity in glial cells. The common theme for these three proteins is their requirement for a proper homeostasis, since their malfunction leads to distinct diseases. We will review here their properties and their role in normal chloride physiology and the pathological consequences of their improper function. This article is protected by copyright. All rights reserved. © 2015 The Authors. The Journal of Physiology © 2015 The Physiological Society.
    The Journal of Physiology 03/2015; 593(18). DOI:10.1113/JP270057 · 5.04 Impact Factor
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    • "This acidification has been widely reported to be produced by vacuolar H + - ATPases (Marshansky and Futai, 2008), coupled to vesicular ClC chloride transporters (Jentsch, 2007) that neutralize the charge gradient produced by proton pumping. Defects in genes encoding these transporters produce spectacular phenotypes in knockout mice or human patients (Kornak et al., 2000; Gü nther et al., 2003; Kasper et al., 2005; Poë t et al., 2006). "
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    ABSTRACT: Vesicular H(+)-ATPases and ClC-chloride transporters are described to acidify intracellular compartments, which also express the highly conserved Na(+)/H(+) exchangers NHE6, NHE7, and NHE9. Mutations of these exchangers cause autism-spectrum disorders and neurodegeneration. NHE6, NHE7, and NHE9 are hypothesized to exchange cytosolic K(+) for H(+) and alkalinize vesicles, but this notion has remained untested in K(+) because their intracellular localization prevents functional measurements. Using proton-killing techniques, we selected a cell line that expresses wild-type NHE7 at the plasma membrane, enabling measurement of the exchanger's transport parameters. We found that NHE7 transports Li(+) and Na(+), but not K(+), is nonreversible in physiological conditions and is constitutively activated by cytosolic H(+). Therefore, NHE7 acts as a proton-loading transporter rather than a proton leak. NHE7 mediates an acidification of intracellular vesicles that is additive to that of V-ATPases and that accelerates endocytosis. This study reveals an unexpected function for vesicular Na(+)/H(+) exchangers and provides clues for understanding NHE-linked neurological disorders.
    Cell Reports 04/2014; 7(3). DOI:10.1016/j.celrep.2014.03.054 · 8.36 Impact Factor
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