Chao Quan, Sangsang Zhu, Rui-Tao Wang, Jiamou Chen, Qiaoli Chen, Min Li, Shu-Yi Su, Q. Du, Minjun Liu, Hong-Yu Wang, Shuai Chen
{"title":"Impaired SERCA2a phosphorylation causes diabetic cardiomyopathy through impinging on cardiac contractility and precursor protein processing","authors":"Chao Quan, Sangsang Zhu, Rui-Tao Wang, Jiamou Chen, Qiaoli Chen, Min Li, Shu-Yi Su, Q. Du, Minjun Liu, Hong-Yu Wang, Shuai Chen","doi":"10.1093/lifemeta/loac013","DOIUrl":null,"url":null,"abstract":"\n Diabetic cardiomyopathy (DCM) is currently a progressive and non-stoppable complication in type 2 diabetic patients. Metabolic insults and insulin resistance are involved in its pathogenesis; however, the underlying mechanisms are still not clearly understood. Here we show that calcium dysregulation can be both a cause and a consequence of cardiac insulin resistance that leads to DCM. A western diet (WD) induces the development of DCM through at least three phases in mice, among which an early phase depends on impaired Thr 484-phosphorylation of sarcoplasmic/endoplasmic reticulum calcium ATPase 2a (SERCA2a) elicited by insulin resistance. Mutation of SERCA2a-Thr 484 to a non-phosphorylatable alanine delays calcium re-uptake into the sarcoplasmic reticulum (SR) in the cardiomyocytes and decreases cardiac function at the baseline. Importantly, this mutation blunts the early phase of DCM, but has no effect on disease progression in the following phases. Interestingly, impairment of SR calcium re-uptake caused by the SERCA2a-Thr 484 mutation inhibited processing of insulin receptor precursor through FURIN convertase, resulting in cardiac insulin resistance. Collectively, these data reveal a bidirectional relationship between insulin resistance and impairment of calcium homeostasis, which may underlie the early pathogenesis of DCM. Our findings have therapeutic implications for early intervention of DCM.","PeriodicalId":74074,"journal":{"name":"Life metabolism","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Life metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/lifemeta/loac013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Diabetic cardiomyopathy (DCM) is currently a progressive and non-stoppable complication in type 2 diabetic patients. Metabolic insults and insulin resistance are involved in its pathogenesis; however, the underlying mechanisms are still not clearly understood. Here we show that calcium dysregulation can be both a cause and a consequence of cardiac insulin resistance that leads to DCM. A western diet (WD) induces the development of DCM through at least three phases in mice, among which an early phase depends on impaired Thr 484-phosphorylation of sarcoplasmic/endoplasmic reticulum calcium ATPase 2a (SERCA2a) elicited by insulin resistance. Mutation of SERCA2a-Thr 484 to a non-phosphorylatable alanine delays calcium re-uptake into the sarcoplasmic reticulum (SR) in the cardiomyocytes and decreases cardiac function at the baseline. Importantly, this mutation blunts the early phase of DCM, but has no effect on disease progression in the following phases. Interestingly, impairment of SR calcium re-uptake caused by the SERCA2a-Thr 484 mutation inhibited processing of insulin receptor precursor through FURIN convertase, resulting in cardiac insulin resistance. Collectively, these data reveal a bidirectional relationship between insulin resistance and impairment of calcium homeostasis, which may underlie the early pathogenesis of DCM. Our findings have therapeutic implications for early intervention of DCM.