Authors
Irina Kramerova, Elena Kudryashova, Gayathri Venkatraman, Melissa J Spencer
Publication date
2005/8/1
Journal
Human Molecular Genetics
Volume
14
Issue
15
Pages
2125-2134
Publisher
Oxford University Press
Description
Mutations in the non-lysosomal cysteine protease calpain 3 cause limb-girdle muscular dystrophy type 2A (LGMD2A). Our previous studies of the calpain 3 knockout mouse (C3KO) suggested a role for calpain 3 in sarcomere formation and remodeling. Calpain 3 may mediate remodeling by cleavage and release of myofibrillar proteins, targeting them for ubiquitination and proteasomal degradation. Loss of proper protein turnover may be the basis for this muscle disease. To test this hypothesis in vivo, we used an experimental model of hindlimb unloading and reloading that has been shown to induce sarcomere remodeling. We showed that the rate of atrophy and especially the rate of growth are decreased in C3KO muscles under conditions promoting sarcomere remodeling. In wild-type mice, an elevated level of ubiquitinated proteins was observed during muscle reloading, which is presumably necessary to …
Total citations
200520062007200820092010201120122013201420152016201720182019202020212022202320241101917141381012961210118910533