Sustained over-expression of calpain-2 induces age-dependent dilated cardiomyopathy in mice through aberrant autophagy  

作　　者：Xiao-yun Ji Dong Zheng Rui Ni Jin-xi Wang Jian-qiang Shao Zer Vue Antentor Hinton Jr Long-Sheng Song Guo-Chang Fan Subrata Chakrabarti Zhao-liang Su Tian-qing Peng 

机构地区：[1]International Genome Center,Jiangsu University,Zhenjiang 212013,China [2]Lawson Health Research Institute,London Health Sciences Centre,London,ON N6A 5W9,Canada [3]Department of Pathology and Laboratory Medicine,Western University,London,ON N6A 5C1,Canada [4]Centre of Clinical Laboratory,the First Affiliated Hospital of Soochow University,Suzhou 215006,China [5]Division of Cardiovascular Medicine,Department of Internal Medicine,Abboud Cardiovascular Research Center,Carver College of Medicine,University of Iowa,Iowa City,IA 52242,USA [6]Central Microscopy Research Facility,University of Iowa,Iowa City,IA 52242,USA [7]Department of Molecular Physiology and Biophysics,Vanderbilt University,Nashville,TN 37232,USA [8]Department of Pharmacology and Systems Physiology,University of Cincinnati College of Medicine,Cincinnati,OH 45267,USA [9]Department of Medicine,Western University,London,ON N6A 5W9,Canada

出　　处：《Acta Pharmacologica Sinica》2022年第11期2873-2884,共12页中国药理学报（英文版）

基　　金：the Doctorial Innovation Projects of Jiangsu Province(Grant No.KYCX17_1816 to XYJ);the Natural Sciences and Engineering Research Council of Canada(RGPIN-2017-04768 to TQP);the Heart&Stroke Foundation of Canada(G-17-0018361 to TQP);the Lawson Internal Research Fund,and Projects of International Cooperation from Jiangsu(BX2019100);International Cooperation and Exchange from Zhenjiang(GJ2020010).

摘　　要：Calpains have been implicated in heart diseases.While calpain-1 has been detrimental to the heart,the role of calpain-2 in cardiac pathology remains controversial.In this study we investigated whether sustained over-expression of calpain-2 had any adverse effects on the heart and the underlying mechanisms.Double transgenic mice(Tg-Capn2/tTA)were generated,which express human CAPN2 restricted to cardiomyocytes.The mice were subjected to echocardiography at age 3,6,8 and 12 months,and their heart tissues and sera were collected for analyses.We showed that transgenic mice over-expressing calpain-2 restricted to cardiomyocytes had normal heart function with no evidence of cardiac pathological remodeling at age 3 months.However,they exhibited features of dilated cardiomyopathy including increased heart size,enlarged heart chambers and heart dysfunction from age 8 months;histological analysis revealed loss of cardiomyocytes replaced by myocardial fibrosis and cardiomyocyte hypertrophy in transgenic mice from age 8 months.These cardiac alterations closely correlated with aberrant autophagy evidenced by significantly increased LC3BII and p62 protein levels and accumulation of autophagosomes in the hearts of transgenic mice.Notably,injection of 3-methyladenine,a well-established inhibitor of autophagy(30 mg/kg,i.p.once every 3 days starting from age 6 months for 2 months)prevented aberrant autophagy,attenuated myocardial injury and improved heart function in the transgenic mice.In cultured cardiomyocytes,over-expression of calpain-2 blocked autophagic flux by impairing lysosomal function.Furthermore,over-expression of calpain-2 resulted in lower levels of junctophilin-2 protein in the heart of transgenic mice and in cultured cardiomyocytes,which was attenuated by 3-methyladenine.In addition,blockade of autophagic flux by bafilomycin A(100 nM)induced a reduction of junctophilin-2 protein in cardiomyocytes.In summary,transgenic over-expression of calpain-2 induces age-dependent dilated cardiomyopathy in mice,which may be me

关 键 词：calpain-2 dilated cardiomyopathy heart dysfunction AUTOPHAGY junctophilin-2 3-methyladenine 

分 类 号：R965[医药卫生—药理学]