Mechanisms and clinical implications of hepatocyte lipoapoptosis

被引:102
作者
Cazanave, Sophie C. [1 ]
Gores, Gregory J. [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Coll Med, Rochester, MN 55905 USA
关键词
BH3-only proteins; CCAAT/enhancer binding homologous protein c-Jun N-terminal kinase; death-receptor; endoplasmic reticulum stress; hepatic steatosis; nonalcoholic steatohepatitis; ENDOPLASMIC-RETICULUM STRESS; FATTY LIVER-DISEASE; NF-KAPPA-B; NONALCOHOLIC STEATOHEPATITIS; INSULIN-RESISTANCE; HEPATIC STEATOSIS; ER STRESS; BH3-ONLY PROTEIN; TRIGLYCERIDE ACCUMULATION; JNK PHOSPHORYLATION;
D O I
10.2217/CLP.09.85
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Nonalcoholic fatty liver disease(NAFLD) is characterized by insulin resistance, elevated serum levels of free fatty acids (FFAs) and fatty infiltration,of the liver. Accumulation of triglycerides in the hepatocyte results from the uptake and esterification of circulating FFAs by the liver. Contrary to current theory, hepatic steatosis appears to be a detoxification process, as FFAs are directly cytotoxic for the hepatocyte and inhibition of triglyceride formation enhances FFAs toxicity. Hepatocyte apoptosis is a,key feature of NAFLD and correlates with disease severity. Since FFA-induced toxicity, or lipoapoptosis, represents a mechanism for the pathogenesis of NAFLD, this article will highlight the cellular pathways contributing to. hepatocyte lipoapoptosis. To date, there is no proven effective therapy for patients with NAFLD and insights into the molecular mediators of lipoapoptosis should help promote effective therapeutic strategies for-this disease.
引用
收藏
页码:71 / 85
页数:15
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