Autophagy and apoptosis in liver injury

被引:352
作者
Wang, Kewei [1 ]
机构
[1] Univ Illinois, Coll Med, Dept Surg, Peoria, IL 61656 USA
关键词
apoptosis; liver injury; mechanism; cross-talk; autophagy; LAMP-2; lysosome-associated membrane protein 2; Vps34; vacuolar protein sorting-34; ER stress; endoplasmic reticulum stress; BH3; Bcl-2 homology domain-3; FADD; Fas-associated protein with death domain; Bcl-x(L); B-cell lymphoma extra long; CSE; cigarette smoke extract; LD; lipid droplets; HBV; hepatitis B virus; HSC; hepatic stellate cells; Beclin-1; Bcl-2-interacting protein-1; HBx; hepatitis B X protein; PI3KC3; phosphatidylinositol-3-kinase class-3; HCV; hepatitis C virus; FFA; free fatty acids; ALT; alanine aminotransferase; PCD; programmed cell death; DNA; Atg; autophagy-related gene; c-FLIP; cellular FLICE-like inhibitor protein; RNA; ribonucleic acid; BNIP; Bcl-2/adenovirus E1B 19 k(d)-interacting protein; MDBs; Mallory-Denk bodies; AMBRA-1; activating molecule in Beclin-1-regulated autophagy; APAP; N-acetyl-p-aminophenol; Drp1; dynamin-related protein 1; Microtubule LC3; microtubule light chain 3; HCC; hepatocellular carcinoma; ATP; adenosine triphosphate; DISC; death-inducing signaling complex; ROS; reactive oxygen species; DRAM; damage regulated autophagic modulator; TNF alpha; tumor necrosis factor-alpha; UVRAG; UV-resistance-associated gene; Bcl-2; B-cell lymphoma-2; siRNA; small interfering RNA; mTOR; mammalian target of rapamycin; Barkor; Beclin-1-associated autophagy-related key regulator; MOMP; mitochondrial outer membrane permiabilization; TUNEL; terminal deoxynucleotidyl transferase dUTP nick-end labeling; CHAPERONE-MEDIATED AUTOPHAGY; STRESS-INDUCED AUTOPHAGY; CELL-DEATH; TUMOR-SUPPRESSOR; HEPATOCELLULAR-CARCINOMA; REGULATES AUTOPHAGY; C-FLIPL; PROTEIN; DEGRADATION; BECLIN;
D O I
10.1080/15384101.2015.1038685
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Apoptosis is a primary characteristic in the pathogenesis of liver disease. Hepatic apoptosis is regulated by autophagic activity. However, mechanisms mediating their interaction remain to be determined. Basal level of autophagy ensures the physiological turnover of old and damaged organelles. Autophagy also is an adaptive response under stressful conditions. Autophagy can control cell fate through different cross-talk signals. A complex interplay between hepatic autophagy and apoptosis determines the degree of hepatic apoptosis and the progression of liver disease as demonstrated by pre-clinical models and clinical trials. This review summarizes recent advances on roles of autophagy that plays in pathophysiology of liver. The autophagic pathway can be a novel therapeutic target for liver disease.
引用
收藏
页码:1631 / 1642
页数:12
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