Chronic heart failure: Ca2+, catabolism, and catastrophic cell death

被引:24
作者
Cho, Geoffrey W. [1 ]
Altamirano, Francisco [1 ]
Hill, Joseph A. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med Cardiol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2016年 / 1862卷 / 04期
关键词
Heart failure; Remodeling; Calcium homeostasis; Autophagy; Apoptosis; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; MITOCHONDRIAL PERMEABILITY TRANSITION; ELEVATION MYOCARDIAL-INFARCTION; INDUCED CARDIAC-HYPERTROPHY; CALCIUM UP-REGULATION; BCL-2; FAMILY-MEMBERS; GROWTH-FACTOR I; SARCOPLASMIC-RETICULUM; RYANODINE RECEPTOR;
D O I
10.1016/j.bbadis.2016.01.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Robust successes have been achieved in recent years in conquering the acutely lethal manifestations of heart disease. Many patients who previously would have died now survive to enjoy happy and productive lives. Nevertheless, the devastating impact of heart disease continues unabated, as the spectrum of disease has evolved with new manifestations. In light of this ever-evolving challenge, insights that culminate in novel therapeutic targets are urgently needed. Here, we review fundamental mechanisms of heart failure, both with reduced (HFrEF) and preserved (HFpEF) ejection fraction. We discuss pathways that regulate cardiomyocyte remodeling and turnover, focusing on Ca2+ signaling, autophagy, and apoptosis. In particular, we highlight recent insights pointing to novel connections among these events. We also explore mechanisms whereby potential therapeutic approaches targeting these processes may improve morbidity and mortality in the devastating syndrome of heart failure. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:763 / 777
页数:15
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