Differential Roles of Unsaturated and Saturated Fatty Acids on Autophagy and Apoptosis in Hepatocytes

脂毒性 自噬 脂肪变性 甘油三酯 细胞凋亡 脂滴 棕榈酸 脂肪酸 饱和脂肪酸 β氧化 化学 脂肪肝 油酸 程序性细胞死亡 非酒精性脂肪肝 生物化学 细胞生物学 生物 内分泌学 内科学 胆固醇 胰岛素抵抗 医学 疾病 胰岛素
作者
Shuang Mei,Hong-Min Ni,Sharon Manley,Abigail Bockus,Karen M. Kassel,James P. Luyendyk,Bryan L. Copple,Wen-Xing Ding
出处
期刊:Journal of Pharmacology and Experimental Therapeutics [American Society for Pharmacology and Experimental Therapeutics]
卷期号:339 (2): 487-498 被引量:284
标识
DOI:10.1124/jpet.111.184341
摘要

Fatty acid-induced lipotoxicity plays a critical role in the pathogenesis of nonalcoholic liver disease. Saturated fatty acids and unsaturated fatty acids have differential effects on cell death and steatosis, but the mechanisms responsible for these differences are not known. Using cultured HepG2 cells and primary mouse hepatocytes, we found that unsaturated and saturated fatty acids differentially regulate autophagy and apoptosis. The unsaturated fatty acid, oleic acid, promoted the formation of triglyceride-enriched lipid droplets and induced autophagy but had a minimal effect on apoptosis. In contrast, the saturated fatty acid, palmitic acid, was poorly converted into triglyceride-enriched lipid droplets, suppressed autophagy, and significantly induced apoptosis. Subsequent studies revealed that palmitic acid-induced apoptosis suppressed autophagy by inducing caspase-dependent Beclin 1 cleavage, indicating cross-talk between apoptosis and autophagy. Moreover, our data suggest that the formation of triglyceride-enriched lipid droplets and induction of autophagy are protective mechanisms against fatty acid-induced lipotoxicity. In line with our in vitro findings, we found that high-fat diet-induced hepatic steatosis was associated with autophagy in the mouse liver. Potential modulation of autophagy may be a novel approach that has therapeutic benefits for obesity-induced steatosis and liver injury.
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