Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophy

Noah Weisleder, Norio Takizawa, Peihui Lin, Xianhua Wang, Chunmei Cao, Yan Zhang, Tao Tan, Christopher Ferrante, Hua Zhu, Pin Jung Chen, Rosalie Yan, Matthew Sterling, Xiaoli Zhao, Moonsun Hwang, Miyuki Takeshima, Chuanxi Cai, Heping Cheng, Hiroshi Takeshima, Rui Ping Xiao, Jianjie Ma

Research output: Contribution to journalArticlepeer-review

179 Scopus citations

Abstract

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.

Original languageEnglish
Article number139ra85
JournalScience Translational Medicine
Volume4
Issue number139
DOIs
StatePublished - Jun 20 2012

ASJC Scopus subject areas

  • General Medicine

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