生物
细胞生物学
化学
调节器
基因
生物物理学
生物化学
作者
Ang Guo,Yihui Wang,Biyi Chen,Yunhao Wang,Jinxiang Yuan,Liyang Zhang,Duane D. Hall,Jennifer D. Wu,Yun‐Bo Shi,Qi Zhu,Cheng Chen,William H. Thiel,Xin Zhan,Robert M. Weiss,Fenghuang Zhan,Catherine A. Musselman,Miles A. Pufall,Weizhong Zhu,Kin Fai Au,Hong Jiang,Mark E. Anderson,Chad E. Grueter,Long‐Sheng Song
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-11-08
卷期号:362 (6421)
被引量:94
标识
DOI:10.1126/science.aan3303
摘要
Protecting the heart Excitation-contraction (E-C) coupling is fundamental to heart contraction. Junctophilin-2 is a structural protein required for formation of the E-C coupling machinery. During heart disease, stress-activated calpain cleaves junctophilin-2, disrupting the E-C coupling machinery and calcium ion signaling, which compromises cell contraction. Guo et al. found that under stress conditions, calpain-mediated cleavage converted full-length junctophilin-2 from a structural protein into a transcriptional regulator that shuttled to the nucleus (see the Perspective by Padmanabhan and Haldar). Furthermore, failing cardiomyocytes in stressed myocardium transduced mechanical information (E-C uncoupling) into transcriptional reprogramming. Science , this issue p. eaan3303 ; see also p. 1359
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