Loss of basement membrane, receptor and cytoskeletal lattices in a laminin-deficient muscular dystrophy
- 15 February 2004
- journal article
- Published by The Company of Biologists in Journal of Cell Science
- Vol. 117 (5) , 735-742
- https://doi.org/10.1242/jcs.00911
Abstract
Basement membrane laminins bearing the α2-subunit interact with α-dystroglycan and β1-integrins, cell-surface receptors that are found within the rectilinear costameric lattices of skeletal muscle sarcolemma. Mutations of the α2 subunit are a major cause of congenital muscular dystrophy. To determine whether the costameres are altered as a result of laminin α2-mutations, the skeletal muscle surface of a dystrophic mouse (dy2J/dy2J) lacking the α2-LN domain was examined by confocal and widefield deconvolution immunomicroscopy. Although the dy2J dystrophic fibers possessed a normal-appearing distribution of α2-laminins and α-dystroglycan within a rectilinear costameric lattice at 6.5 weeks of age, by 11 weeks the surface architecture of these components were found to be disorganized, with frequent effacement of the circumferential and longitudinal lattice striations. The defect in the lattice organization was also noted to be a characteristic of type IV collagen, nidogen, perlecan, β1D-integrin, dystrophin and vinculin. The development of this pattern change occurring only after birth suggests that although α2-laminins are not essential for the initial assembly of the costameric framework, they play a role in maintaining the stability and organization of the framework.Keywords
This publication has 32 references indexed in Scilit:
- The Basement Membrane/Basal Lamina of Skeletal MuscleJournal of Biological Chemistry, 2003
- The laminin α2 expressed by dystrophic dy2J mice is defective in its ability to form polymersCurrent Biology, 1999
- Three-Dimensional Imaging by Deconvolution MicroscopyMethods, 1999
- Distribution of ten laminin chains in dystrophic and regenerating musclesNeuromuscular Disorders, 1999
- Laminin Polymerization Induces a Receptor–Cytoskeleton NetworkThe Journal of cell biology, 1999
- Extensive but Coordinated Reorganization of the Membrane Skeleton in Myofibers of Dystrophic (mdx) MiceThe Journal of cell biology, 1999
- Role of α-Dystroglycan as a Schwann Cell Receptor for Mycobacterium lepraeScience, 1998
- Spatial and temporal expression of the β1D integrin during mouse developmentDevelopmental Dynamics, 1997
- Developmental expression of perlecan during murine embryogenesisDevelopmental Dynamics, 1997
- Costameres are sites of force transmission to the substratum in adult rat cardiomyocytes.The Journal of cell biology, 1992