| Literature DB >> 31033952 |
Xuan Su1, Yan Shen2, Yue Jin1, Meng Jiang3, Neal Weintraub2, Yaoliang Tang4.
Abstract
Duchene Muscular Dystrophy (DMD) is an X-linked recessive genetic disease caused by a lack of functional dystrophin protein. The disease cannot be cured, and as the disease progresses, the patient develops symptoms of dilated cardiomyopathy, arrhythmia, and congestive heart failure. The DMDMDX mutant mice do not express dystrophin, and are commonly used as a mouse model of DMD. In our recent study, we observed that intramyocardial injection of wide type (WT)-myogenic progenitor cells-derived exosomes (MPC-Exo) transiently restored the expression of dystrophin in the myocardium of DMDMDX mutant mice, which was associated with a transient improvement in cardiac function suggesting that WT-MPC-Exo may provide an option to relieve the cardiac symptoms of DMD. This article describes the technique of MPC-Exo purification and transplantation into hearts of DMDMDX mutant mice.Entities:
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Year: 2019 PMID: 31033952 PMCID: PMC7193702 DOI: 10.3791/59320
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355