Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease

Neuromuscul Disord. 2000 Jan;10(1):16-23. doi: 10.1016/s0960-8966(99)00066-8.

Abstract

Muscle-eye-brain disease belongs to congenital muscular dystrophies with central nervous system abnormalities. The etiology of MEB is still unknown, but abnormal immunoreactivity for laminin-2 has been reported. To evaluate disease progression in muscle tissue, 32 biopsy specimens from 17 muscle-eye-brain patients were analysed. The samples of four patients were studied by immunohistochemical techniques and by quantitative Western blotting. The samples showed a great variation in the muscle pathology. Regenerative fibers and mild fiber size variation were present in over 60%. At infancy, necrotic and regenerative fibers were common, while fat infiltration was the most prominent finding in the age group over five years. In quantitative studies, the amount of laminin alpha 2 chain was clearly reduced to 10-20% of normal. In contrast, laminin beta 2 chain was overexpressed in the Western blotting studies. These findings may reflect a yet unidentified primary disturbance in the basement membrane composition and function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Blotting, Western
  • Cytoskeletal Proteins / metabolism*
  • Dystroglycans
  • Dystrophin / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Laminin / metabolism
  • Male
  • Membrane Glycoproteins / metabolism
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Muscles / metabolism*
  • Muscles / pathology*
  • Muscular Dystrophies / congenital
  • Muscular Dystrophies / metabolism*
  • Muscular Dystrophies / pathology*

Substances

  • Cytoskeletal Proteins
  • DAG1 protein, human
  • Dystrophin
  • Laminin
  • Membrane Glycoproteins
  • Membrane Proteins
  • Dystroglycans