Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency

Am J Pathol. 2002 Jan;160(1):265-70. doi: 10.1016/S0002-9440(10)64370-2.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Caveolae / physiology*
  • Caveolae / ultrastructure
  • Caveolin 3
  • Caveolins / deficiency*
  • Child
  • Freeze Fracturing
  • Humans
  • Immunohistochemistry
  • Lanthanum
  • Microscopy, Electron
  • Middle Aged
  • Muscle, Skeletal / ultrastructure*
  • Muscular Dystrophies / metabolism*
  • Muscular Dystrophies / pathology*
  • Staining and Labeling

Substances

  • Caveolin 3
  • Caveolins
  • Lanthanum