In vivo characterization of skeletal muscle function in nebulin-deficient mice

被引:4
|
作者
Gineste, Charlotte [1 ]
Ogier, Augustin C. [2 ]
Varlet, Isabelle [1 ]
Hourani, Zaynab [3 ]
Bernard, Monique [1 ]
Granzier, Henk [3 ]
Bendahan, David [1 ]
Gondin, Julien [1 ,4 ]
机构
[1] Aix Marseille Univ, CRMBM, CNRS, Marseille, France
[2] Aix Marseille Univ, Univ Toulon, LIS, CNRS, Marseille, France
[3] Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ USA
[4] Univ Claude Bernard, Inst NeuroMyoGene, UMR CNRS 5310, INSERM U1217, Lyon, France
关键词
fatigue; in vivo; muscle wasting; muscle weakness; nemaline myopathy; neuromuscular disorder; THIN FILAMENT LENGTH; NEMALINE MYOPATHY; CREATINE-KINASE; MOUSE MODEL; EXPRESSION; SARCOMERE; GENE; WEAKNESS;
D O I
10.1002/mus.26798
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction The conditional nebulin knockout mouse is a new model mimicking nemaline myopathy, a rare disease characterized by muscle weakness and rods within muscle fibers. We investigated the impact of nebulin (NEB) deficiency on muscle function in vivo. Methods Conditional nebulin knockout mice and control littermates were studied at 10 to 12 months. Muscle function (force and fatigue) and anatomy (muscles volume and fat content) were measured in vivo. Myosin heavy chain (MHC) composition and nebulin (NEB) protein expression were assessed by protein electrophoresis. Results Conditional nebulin knockout mice displayed a lower NEB level (-90%) leading to a 40% and 45% reduction in specific maximal force production and muscles volume, respectively. Nebulin deficiency was also associated with higher resistance to fatigue and increased MHC I content. Discussion Adult nebulin-deficient mice displayed severe muscle atrophy and weakness in vivo related to a low NEB content but an improved fatigue resistance due to a slower contractile phenotype.
引用
收藏
页码:416 / 424
页数:9
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