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Blocking MG53S255 Phosphorylation Protects Diabetic Heart From Ischemic Injury

Circulation research, 2022-12, Vol.131 (12), p.962-976 [Peer Reviewed Journal]

2022 The Authors. 2022 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.122.321055 ;PMID: 36337049

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  • Title:
    Blocking MG53S255 Phosphorylation Protects Diabetic Heart From Ischemic Injury
  • Author: Lv, Fengxiang ; Wang, Yingfan ; Shan, Dan ; Guo, Sile ; Chen, Gengjia ; Jin, Li ; Zheng, Wen ; Feng, Han ; Zeng, Xiaohu ; Zhang, Shuo ; Zhang, Yan ; Hu, Xinli ; Xiao, Rui-Ping
  • Subjects: Original Research
  • Is Part Of: Circulation research, 2022-12, Vol.131 (12), p.962-976
  • Description: BACKGROUNDAs an integral component of cell membrane repair machinery, MG53 (mitsugumin 53) is important for cardioprotection induced by ischemia preconditioning and postconditioning. However, it also impairs insulin signaling via its E3 ligase activity-mediated ubiquitination-dependent degradation of IR (insulin receptor) and IRS1 (insulin receptor substrate 1) and its myokine function-induced allosteric blockage of IR. Here, we sought to develop MG53 into a cardioprotection therapy by separating its detrimental metabolic effects from beneficial actions. METHODSUsing immunoprecipitation-mass spectrometry, site-specific mutation, in vitro kinase assay, and in vivo animal studies, we investigated the role of MG53 phosphorylation at serine 255 (S255). In particular, utilizing recombinant proteins and gene knock-in approaches, we evaluated the potential therapeutic effect of MG53-S255A mutant in treating cardiac ischemia/reperfusion injury in diabetic mice. RESULTSWe identified S255 phosphorylation as a prerequisite for MG53 E3 ligase activity. Furthermore, MG53S255 phosphorylation was mediated by GSK3β (glycogen synthase kinase 3 beta) and markedly elevated in the animal models with metabolic disorders. Thus, IR-IRS1-GSK3β-MG53 formed a vicious cycle in the pathogenesis of metabolic disorders where aberrant insulin signaling led to hyper-activation of GSK3β, which in turn, phosphorylated MG53 and enhanced its E3 ligase activity, and further impaired insulin sensitivity. Importantly, S255A mutant eliminated the E3 ligase activity while retained cell protective function of MG53. Consequently, the S255A mutant, but not the wild type MG53, protected the heart against ischemia/reperfusion injury in db/db mice with advanced diabetes, although both elicited cardioprotection in normal mice. Moreover, in S255A knock-in mice, S255A mutant also mitigated ischemia/reperfusion-induced myocardial damage in the diabetic setting. CONCLUSIONSS255 phosphorylation is a biased regulation of MG53 E3 ligase activity. The MG53-S255A mutant provides a promising approach for the treatment of acute myocardial injury, especially in patients with metabolic disorders.
  • Publisher: Hagerstown, MD: Lippincott Williams & Wilkins
  • Language: English
  • Identifier: ISSN: 0009-7330
    EISSN: 1524-4571
    DOI: 10.1161/CIRCRESAHA.122.321055
    PMID: 36337049
  • Source: GFMER Free Medical Journals
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