ER Protein Quality Control and the Unfolded Protein Response in the Heart

被引:32
作者
Arrieta, A. [1 ,2 ]
Blackwood, E. A. [1 ,2 ]
Glembotski, C. C. [1 ,2 ]
机构
[1] San Diego State Univ, Inst Heart, San Diego, CA 92182 USA
[2] San Diego State Univ, Dept Biol, San Diego, CA 92182 USA
来源
COORDINATING ORGANISMAL PHYSIOLOGY THROUGH THE UNFOLDED PROTEIN RESPONSE | 2018年 / 414卷
关键词
ENDOPLASMIC-RETICULUM STRESS; CARDIAC-HYPERTROPHY; OXIDATIVE STRESS; O-GLCNAC; CALCIUM; DYSFUNCTION; ATF6; ACTIVATION; MECHANISMS; APOPTOSIS;
D O I
10.1007/82_2017_54
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiac myocytes are the cells responsible for the robust ability of the heart to pump blood throughout the circulatory system. Cardiac myocytes grow in response to a variety of physiological and pathological conditions; this growth challenges endoplasmic reticulum-protein quality control (ER-PQC), a major feature of which includes the unfolded protein response (UPR). ER-PQC and the UPR in cardiac myocytes growing under physiological conditions, including normal development, exercise, and pregnancy, are sufficient to support hypertrophic growth of each cardiac myocyte. However, the ER-PQC and UPR are insufficient to respond to the challenge of cardiac myocyte growth under pathological conditions, including myocardial infarction and heart failure. In part, this insufficiency is due to a continual decline in the expression levels of important adaptive UPR components as a function of age and during myocardial pathology. This chapter will discuss the physiological and pathological conditions unique to the heart that involves ER-PQC, and whether the UPR is adaptive or maladaptive under these circumstances.
引用
收藏
页码:193 / 213
页数:21
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