Functions of autophagy in normal and diseased liver

被引:443
作者
Czaja, Mark J. [1 ]
Ding, Wen-Xing [2 ]
Donohue, Terrence M., Jr. [3 ]
Friedman, Scott L. [4 ]
Kim, Jae-Sung [5 ]
Komatsu, Masaaki [6 ]
Lemasters, John J. [7 ,8 ]
Lemoine, Antoinette [9 ]
Lin, Jiandie D. [10 ,11 ]
Ou, Jing-Hsiung James [12 ]
Perlmutter, David H. [13 ,14 ,15 ]
Randall, Glenn [16 ]
Ray, Ratna B. [17 ]
Tsung, Allan [18 ]
Yin, Xiao-Ming [19 ]
机构
[1] Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Dept Med, Bronx, NY 10467 USA
[2] Univ Kansas, Med Ctr, Dept Pharmacol Toxicol & Therapeut, Kansas City, KS 66103 USA
[3] VA Nebraska Western Iowa Hlth Care Syst, Dept Vet Affairs, Liver Study Unit, Omaha, NE USA
[4] Icahn Sch Med Mt Sinai, Div Liver Dis, New York, NY USA
[5] Univ Florida, Coll Med, Dept Surg, Gainesville, FL USA
[6] Tokyo Metropolitan Inst Med Sci, Protein Metab Project, Tokyo 113, Japan
[7] Med Univ S Carolina, Ctr Cell Death Injury & Regenerat, Dept Drug Discovery & Biomed Sci, Charleston, SC 29425 USA
[8] Med Univ S Carolina, Ctr Cell Death Injury & Regenerat, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[9] Hop Paul Brousse, AP HP, Serv Biochim & Biol Mol, Villejuif, France
[10] Univ Michigan, Med Ctr, Inst Life Sci, Ann Arbor, MI USA
[11] Univ Michigan, Med Ctr, Dept Cell & Dev Biol, Ann Arbor, MI USA
[12] Univ So Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[13] Univ Pittsburgh, Sch Med, Dept Pediat, Pittsburgh, PA USA
[14] Univ Pittsburgh, Sch Med, Dept Cell Biol, Pittsburgh, PA USA
[15] UPMC, Childrens Hosp Pittsburgh, Pittsburgh, PA USA
[16] Univ Chicago, Dept Microbiol, Div Biol Sci, Chicago, IL 60637 USA
[17] St Louis Univ, Dept Pathol, Doisy Res Ctr, St Louis, MO 63103 USA
[18] Univ Pittsburgh, Med Ctr, Div Hepatobiliary & Pancreat Surg, Pittsburgh, PA USA
[19] Indiana Univ, Sch Med, Dept Pathol & Lab Med, Indianapolis, IN USA
基金
美国国家卫生研究院;
关键词
autophagy; liver; hepatocyte; hepatitis; ischemia/reperfusion; liver injury; hepatotoxin; hepatocellular carcinoma; drug toxicity; HEPATITIS-C VIRUS; MITOCHONDRIAL PERMEABILITY TRANSITION; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; CHAPERONE-MEDIATED AUTOPHAGY; TOLL-LIKE RECEPTORS; NF-KAPPA-B; CELL-DEATH; HEPATOCELLULAR-CARCINOMA; RAT-LIVER;
D O I
10.4161/auto.25063
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy has emerged as a critical lysosomal pathway that maintains cell function and survival through the degradation of cellular components such as organelles and proteins. Investigations specifically employing the liver or hepatocytes as experimental models have contributed significantly to our current knowledge of autophagic regulation and function. The diverse cellular functions of autophagy, along with unique features of the liver and its principal cell type the hepatocyte, suggest that the liver is highly dependent on autophagy for both normal function and to prevent the development of disease states. However, instances have also been identified in which autophagy promotes pathological changes such as the development of hepatic fibrosis. Considerable evidence has accumulated that alterations in autophagy are an underlying mechanism of a number of common hepatic diseases including toxin-, drug- and ischemia/reperfusion-induced liver injury, fatty liver, viral hepatitis and hepatocellular carcinoma. This review summarizes recent advances in understanding the roles that autophagy plays in normal hepatic physiology and pathophysiology with the intent of furthering the development of autophagy-based therapies for human liver diseases.
引用
收藏
页码:1131 / 1158
页数:28
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