Muscular dystrophy: centronucleation may reflect a compensatory activation of defective myonuclei
- PMID: 9570514
- DOI: 10.1007/BF02253356
Muscular dystrophy: centronucleation may reflect a compensatory activation of defective myonuclei
Abstract
Muscular dystrophy has long been believed to be characterized by degeneration and abortive regeneration of muscle fibers (the muscle degeneration theory), but unfortunately its pathogenesis is still unclear and an effective treatment has yet to be developed. As a challenge to the theory, we have proposed an alternative muscle-defective-growth theory and a further bone muscle growth imbalance hypothesis supposing possible defects in bone-growth-dependent muscle growth based on our findings in hereditary dystrophic dy mice (C57BL/6J dy/dy). This review presents some new insights into the pathogenesis of the disease along with our hypothesis, focusing on the physiological meaning of centronucleation, one of the major pathological changes commonly observed in dystrophic muscles of man and experimental animals.
Similar articles
-
Elimination of myostatin does not combat muscular dystrophy in dy mice but increases postnatal lethality.Am J Pathol. 2005 Feb;166(2):491-7. doi: 10.1016/S0002-9440(10)62271-7. Am J Pathol. 2005. PMID: 15681832 Free PMC article.
-
Muscular degeneration in Duchenne's dystrophy may be caused by a mitochondrial defect.Med Hypotheses. 1995 Apr;44(4):298-300. doi: 10.1016/0306-9877(95)90184-1. Med Hypotheses. 1995. PMID: 7666833
-
Dystrophin deficiency, altered cell signalling and fibre hypertrophy.Neuromuscul Disord. 1994 Jul;4(4):305-15. doi: 10.1016/0960-8966(94)90066-3. Neuromuscul Disord. 1994. PMID: 7981587 Review.
-
Early skeletal muscle pathology and disease progress in the dy3K/dy3K mouse model of congenital muscular dystrophy with laminin α2 chain-deficiency.Sci Rep. 2019 Oct 4;9(1):14324. doi: 10.1038/s41598-019-50550-0. Sci Rep. 2019. PMID: 31586140 Free PMC article.
-
Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies.Annu Rev Physiol. 2009;71:37-57. doi: 10.1146/annurev.physiol.010908.163216. Annu Rev Physiol. 2009. PMID: 18808326 Review.
Cited by
-
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy.Sci Rep. 2020 Aug 21;10(1):14070. doi: 10.1038/s41598-020-70987-y. Sci Rep. 2020. PMID: 32826942 Free PMC article.
-
Green tea extract decreases muscle pathology and NF-kappaB immunostaining in regenerating muscle fibers of mdx mice.Clin Nutr. 2010 Jun;29(3):391-8. doi: 10.1016/j.clnu.2009.10.001. Epub 2009 Nov 7. Clin Nutr. 2010. PMID: 19897286 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Medical
Research Materials