Zebrafish models of collagen VI-related myopathies.
Zebrafish models of collagen VI-related myopathies.
复制标题
DOI：
10.1093/hmg/ddq126
复制
发表时间：
2010-06-15
影响因子：
3.5
通讯作者：
Dowling JJ
中科院分区：
文献类型：
--
作者：
Telfer WR;Busta AS;Bonnemann CG;Feldman EL;Dowling JJ
Collagen VI is an integral part of the skeletal muscle extracellular matrix, providing mechanical stability and facilitating matrix-dependent cell signaling. Mutations in collagen VI result in either Ullrich congenital muscular dystrophy (UCMD) or Bethlem myopathy (BM), with UCMD being clinically more severe. Recent studies demonstrating increased apoptosis and abnormal mitochondrial function in Col6a1 knockout mice and in human myoblasts have provided the first mechanistic insights into the pathophysiology of these diseases. However, how loss of collagen VI causes mitochondrial dysfunction remains to be understood. Progress is hindered in part by the lack of an adequate animal model for UCMD, as knockout mice have a mild motor phenotype. To further the understanding of these disorders, we have generated zebrafish models of the collagen VI myopathies. Morpholinos designed to exon 9 of col6a1 produced a severe muscle disease reminiscent of UCMD, while ones to exon 13 produced a milder phenotype similar to BM. UCMD-like zebrafish have increased cell death and abnormal mitochondria, which can be attenuated by treatment with the proton pump modifier cyclosporin A (CsA). CsA improved the motor deficits in UCMD-like zebrafish, but failed to reverse the sarcolemmal membrane damage. In all, we have successfully generated the first vertebrate model matching the clinical severity of UCMD and demonstrated that CsA provides phenotypic improvement, thus corroborating data from knockout mice supporting the use of mitochondrial permeability transition pore modifiers as therapeutics in patients, and providing proof of principle for the utility of the zebrafish as a powerful preclinical model.
登录
查看更多内容
影响因子：
4.5
作者：
Dowling, James J.;Vreede, Andrew P.;Low, Sean E.;Gibbs, Elizabeth M.;Kuwada, John Y.;Bonnemann, Carsten G.;Feldman, Eva L.
通讯作者：
Feldman, Eva L.
影响因子：
30.8
作者：
Irwin, WA;Bergamin, N;Bonaldo, P
通讯作者：
Bonaldo, P
影响因子：
4.8
作者：
COLOMBATTI, A;MUCIGNAT, MT;BONALDO, P
通讯作者：
BONALDO, P
影响因子：
3.5
作者：
Bonaldo, P;Braghetta, P;Bressan, GM
通讯作者：
Bressan, GM
影响因子：
14.5
作者：
Jöbsis, GJ;Boers, JM;de Visser, M
通讯作者：
de Visser, M