TY - JOUR
T1 - Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy
AU - Weisleder, Noah
AU - Takizawa, Norio
AU - Lin, Peihui
AU - Wang, Xianhua
AU - Cao, Chunmei
AU - Zhang, Yan
AU - Tan, Tao
AU - Ferrante, Christopher
AU - Zhu, Hua
AU - Chen, Pin Jung
AU - Yan, Rosalie
AU - Sterling, Matthew
AU - Zhao, Xiaoli
AU - Hwang, Moonsun
AU - Takeshima, Miyuki
AU - Cai, Chuanxi
AU - Cheng, Heping
AU - Takeshima, Hiroshi
AU - Xiao, Rui Ping
AU - Ma, Jianjie
PY - 2012/6/20
Y1 - 2012/6/20
N2 - Mitsugumin 53 (MG53), a muscle-specific TRIM family protein, is an essential component of the cell membrane repair machinery. Here, we examined the translational value of targeting MG53 function in tissue repair and regenerative medicine. Although native MG53 protein is principally restricted to skeletal and cardiac muscle tissues, beneficial effects that protect against cellular injuries are present in nonmuscle cells with overexpression of MG53. In addition to the intracellular action of MG53, injury to the cell membrane exposes a signal that can be detected by MG53, allowing recombinant MG53 protein to repair membrane damage when provided in the extracellular space. Recombinant human MG53 (rhMG53) protein purified from Escherichia coli fermentation provided dose-dependent protection against chemical, mechanical, or ultraviolet-induced damage to both muscle and nonmuscle cells. Injection of rhMG53 through multiple routes decreased muscle pathology in the mdx dystrophic mouse model. Our data support the concept of targeted cell membrane repair in regenerative medicine, and present MG53 protein as an attractive biological reagent for restoration of membrane repair defects in human diseases.
AB - Mitsugumin 53 (MG53), a muscle-specific TRIM family protein, is an essential component of the cell membrane repair machinery. Here, we examined the translational value of targeting MG53 function in tissue repair and regenerative medicine. Although native MG53 protein is principally restricted to skeletal and cardiac muscle tissues, beneficial effects that protect against cellular injuries are present in nonmuscle cells with overexpression of MG53. In addition to the intracellular action of MG53, injury to the cell membrane exposes a signal that can be detected by MG53, allowing recombinant MG53 protein to repair membrane damage when provided in the extracellular space. Recombinant human MG53 (rhMG53) protein purified from Escherichia coli fermentation provided dose-dependent protection against chemical, mechanical, or ultraviolet-induced damage to both muscle and nonmuscle cells. Injection of rhMG53 through multiple routes decreased muscle pathology in the mdx dystrophic mouse model. Our data support the concept of targeted cell membrane repair in regenerative medicine, and present MG53 protein as an attractive biological reagent for restoration of membrane repair defects in human diseases.
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U2 - 10.1126/scitranslmed.3003921
DO - 10.1126/scitranslmed.3003921
M3 - Article
C2 - 22723464
AN - SCOPUS:84862907349
SN - 1946-6234
VL - 4
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 139
M1 - 139ra85
ER -