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Am J Pathol ; 160(1): 265-70, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11786420

RESUMO

Caveolin-3, a muscle specific caveolin-related protein, is the principal structural protein of caveolar membranes. We have recently identified an autosomal dominant form of limb girdle muscular dystrophy (LGMD-1C) that is due to caveolin-3 deficiency and caveolin-3 gene mutations. Here, we studied by electron microscopy, including freeze-fracture and lanthanum staining, the distribution of caveolae and the organization of the T-tubule system in caveolin-3 deficient human muscle fibers. We found a severe impairment of caveolae formation at the muscle cell surface, demonstrating that caveolin-3 is essential for the formation and organization of caveolae in muscle fibers. In addition, we also detected a striking disorganization of the T-system openings at the sub-sarcolemmal level in LGMD-1C muscle fibers. These observations provide new perspectives in our understanding of the role of caveolin-3 in muscle and of the pathogenesis of muscle weakness in caveolin-3 deficient muscle.


Assuntos
Cavéolas/fisiologia , Caveolinas/deficiência , Músculo Esquelético/ultraestrutura , Distrofias Musculares/metabolismo , Distrofias Musculares/patologia , Adolescente , Cavéolas/ultraestrutura , Caveolina 3 , Criança , Técnica de Fratura por Congelamento , Humanos , Imuno-Histoquímica , Lantânio , Microscopia Eletrônica , Pessoa de Meia-Idade , Coloração e Rotulagem
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