Journal
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
Volume 34, Issue 5-6, Pages 395-405Publisher
SPRINGER
DOI: 10.1007/s10974-013-9362-9
Keywords
Dystrophic cardiomyopathy; Dystrophin; Utrophin; Alpha-dystroglycan; Glycosylation
Categories
Funding
- NHLBI NIH HHS [K08 HL102066, R01 HL114832] Funding Source: Medline
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Heart disease is a leading cause of death in patients with Duchenne muscular dystrophy (DMD). Patients with DMD lack the protein dystrophin, which is widely expressed in striated muscle. In skeletal muscle, the loss of dystrophin results in dramatically decreased expression of the dystrophin associated glycoprotein complex (DGC). Interestingly, in the heart the DGC is normally expressed without dystrophin; this has been attributed to presence of the dystrophin homologue utrophin. We demonstrate here that neither utrophin nor dystrophin are required for the expression of the cardiac DGC. However, alpha-dystroglycan (alpha-DG), a major component of the DGC, is differentially glycosylated in dystrophin-(mdx) and dystrophin-/utrophin-(dko) deficient mouse hearts. In both models the altered alpha-DG retains laminin binding activity, but has an altered localization at the sarcolemma. In hearts lacking both dystrophin and utrophin, the alterations in alpha-DG glycosylation are even more dramatic with changes in gel migration equivalent to 24 +/- A 3 kDa. These data show that the absence of dystrophin and utrophin alters the processing of alpha-DG; however it is not clear if these alterations are a consequence of the loss of a direct interaction with dystrophin/utrophin or results from an indirect response to the presence of severe pathology. Recently there have been great advances in our understanding of the glycosylation of alpha-DG regarding its role as a laminin receptor. Here we present data that alterations in glycosylation occur in the hearts of animal models of DMD, but these changes do not affect laminin binding. The physiological consequences of these alterations remain unknown, but may have significant implications for the development of therapies for DMD.
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