Expression profiling in the muscular dystrophies: identification of novel aspects of molecular pathophysiology.

Abstract

We used expression profiling to define the pathophysiological cascades involved in the progression of two muscular dystrophies with known primary biochemical defects, dystrophin deficiency (Duchenne muscular dystrophy) and alpha-sarcoglycan deficiency (a dystrophin-associated protein). We employed a novel protocol for expression profiling in human tissues using mixed samples of multiple patients and iterative comparisons of duplicate datasets. We found evidence for both incomplete differentiation of patient muscle, and for dedifferentiation of myofibers to alternative lineages with advancing age. One developmentally regulated gene characterized in detail, alpha-cardiac actin, showed abnormal persistent expression after birth in 60% of Duchenne dystrophy myofibers. The majority of myofibers ( approximately 80%) remained strongly positive for this protein throughout the course of the disease. Other developmentally regulated genes that showed widespread overexpression in these muscular dystrophies included embryonic myosin heavy chain, versican, acetylcholine receptor alpha-1, secreted protein, acidic and rich in cysteine/osteonectin, and thrombospondin 4. We hypothesize that the abnormal Ca(2)+ influx in dystrophin- and alpha-sarcoglycan-deficient myofibers leads to altered developmental programming of developing and regenerating myofibers. The finding of upregulation of HLA-DR and factor XIIIa led to the novel identification of activated dendritic cell infiltration in dystrophic muscle; these cells mediate immune responses and likely induce microenvironmental changes in muscle. We also document a general metabolic crisis in dystrophic muscle, with large scale downregulation of nuclear-encoded mitochondrial gene expression. Finally, our expression profiling results show that primary genetic defects can be identified by a reduction in the corresponding RNA.

• Authors: Y W Chen, P Zhao, R Borup, E P Hoffman
• Journal: The Journal of cell biology (J Cell Biol) Vol. 151 Issue 6 Pg. 1321-36 (Dec 11 2000) ISSN: 0021-9525 [Print] United States
• PMID: 11121445 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Actins
• Chondroitin Sulfate Proteoglycans
• Cytoskeletal Proteins
• Dystrophin
• HLA-DR Antigens
• Lectins, C-Type
• Membrane Glycoproteins
• Osteonectin
• Sarcoglycans
• Thrombospondins
• VCAN protein, human
• thrombospondin 4
• Versicans
• Factor VIIIa
• Myosin Heavy Chains

Topics

• Actins (analysis, genetics)
• Biopsy
• Child
• Chondroitin Sulfate Proteoglycans (analysis, genetics)
• Cytoskeletal Proteins (deficiency)
• Dystrophin (deficiency)
• Factor VIIIa (analysis, genetics)
• Female
• Gene Expression Profiling (methods)
• HLA-DR Antigens (analysis, genetics)
• Humans
• Lectins, C-Type
• Male
• Membrane Glycoproteins (deficiency)
• Muscle, Skeletal (chemistry)
• Muscular Dystrophies (etiology, genetics)
• Muscular Dystrophy, Duchenne (etiology, genetics)
• Myosin Heavy Chains (analysis, genetics)
• Oligonucleotide Array Sequence Analysis
• Osteonectin (analysis, genetics)
• Sarcoglycans
• Thrombospondins (analysis, genetics)
• Versicans