Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/198231
Type: Artigo de periódico
Title: Sarcoplasmic-endoplasmic-reticulum Ca2+-atpase And Calsequestrin Are Overexpressed In Spared Intrinsic Laryngeal Muscles Of Dystrophin-deficient Mdx Mice.
Author: Ferretti, Renato
Marques, Maria Julia
Pertille, Adriana
Santo Neto, Humberto
Abstract: In the mdx mouse model of Duchenne muscular dystrophy, the lack of dystrophin is associated with increased calcium levels and skeletal muscle myonecrosis. The intrinsic laryngeal muscles (ILM) are protected and do not undergo myonecrosis. We investigated whether this protection is related to an increased expression of calcium-binding proteins, which may protect against the elevated calcium levels seen in dystrophic fibers. The expression of sarcoplasmic-endoplasmic-reticulum Ca(2+)-ATPase and calsequestrin was examined in ILM and in nonspared limb muscles of control and mdx mice using immunofluorescence and immunoblotting. Dystrophic ILM presented a significant increase in the proteins studied when compared to controls. The increase of Ca(2+)-handling proteins in dystrophic ILM may permit better maintenance of calcium homeostasis, with the consequent absence of myonecrosis. The results further support the concept that abnormal Ca(2+)-handling is involved in dystrophinopathies. Muscle Nerve, 2009.
Subject: Animals
Calsequestrin
Dystrophin
Gene Expression Regulation
Laryngeal Muscles
Mice
Mice, Inbred C57bl
Mice, Inbred Mdx
Sarcoplasmic Reticulum Calcium-transporting Atpases
Rights: fechado
Identifier DOI: 10.1002/mus.21154
Address: http://www.ncbi.nlm.nih.gov/pubmed/19301368
Date Issue: 2009
Appears in Collections:Unicamp - Artigos e Outros Documentos

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