%0 Journal Article
%T Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
%A Renzhi Han
%A Erik P Rader
%A Jennifer R Levy
%A Dimple Bansal
%A Kevin P Campbell
%J Skeletal Muscle
%D 2011
%I BioMed Central
%R 10.1186/2044-5040-1-35
%X To test our hypothesis, we generated dystrophin/dysferlin double-knockout (DKO) mice by breeding mdx mice with dysferlin-null mice and analyzed the effects of a combined deficiency of dysferlin and dystrophin on muscle pathology and sarcolemmal integrity.The DKO mice exhibited more severe muscle pathology than either mdx mice or dysferlin-null mice, and, importantly, the onset of the muscle pathology occurred much earlier than it did in dysferlin-deficient mice. The DKO mice showed muscle pathology of various skeletal muscles, including the mandible muscles, as well as a greater number of regenerating muscle fibers, higher serum creatine kinase levels and elevated Evans blue dye uptake into skeletal muscles. Lengthening contractions caused similar force deficits, regardless of dysferlin expression. However, the rate of force recovery within 45 minutes following lengthening contractions was hampered in DKO muscles compared to mdx muscles or dysferlin-null muscles, suggesting that dysferlin is required for the initial recovery from lengthening contraction-induced muscle injury of the dystrophin-glycoprotein complex-compromised muscles.The results of our study suggest that dysferlin-mediated membrane repair helps to limit the dystrophic changes in dystrophin-deficient skeletal muscle. Dystrophin deficiency unmasks the function of dysferlin in membrane repair during lengthening contractions. Dystrophin/dysferlin-deficient mice provide a very useful model with which to evaluate the effectiveness of therapies designed to treat dysferlin deficiency.Duchenne muscular dystrophy (DMD) is an X-linked recessive disease affecting approximately 1 in 3, 500 males and is caused by defects in the dystrophin gene [1]. Dystrophin is an integral component of the dystrophin-glycoprotein complex (DGC) and is localized to the inner surface of the plasma membrane [2]. Dystrophin plays an important role in linking the cytoskeleton to the sarcolemma through the direct interactions of its N-t
%K dysferlin
%K dystrophin
%K membrane repair
%K sarcolemmal integrity
%U http://www.skeletalmusclejournal.com/content/1/1/35