Sui Yong-Heng, Luo Wen-Jing, Xu Qin-Yu, Hua Jing
Yong-Heng Sui, Wen-Jing Luo, Qin-Yu Xu, Jing Hua, Division of Gastroenterology and Hepatology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Institute of Digestive Disease, Shanghai 200127, China.
World J Gastroenterol. 2016 Feb 28;22(8):2533-44. doi: 10.3748/wjg.v22.i8.2533.
To investigate the effect of different dietary fatty acids on hepatic inflammasome activation.
Wild-type C57BL/6 mice were fed either a high-fat diet or polyunsaturated fatty acid (PUFA)-enriched diet. Primary hepatocytes were treated with either saturated fatty acids (SFAs) or PUFAs as well as combined with lipopolysaccharide (LPS). The expression of NOD-like receptor protein 3 (NLRP3) inflammasome, peroxisome proliferator-activated receptor-γ and nuclear factor-kappa B (NF-κB) was determined by real-time PCR and Western blot. The activity of Caspase-1 and interleukine-1β production were measured.
High-fat diet-induced hepatic steatosis was sufficient to induce and activate hepatic NLRP3 inflammasome. SFA palmitic acid (PA) directly activated NLRP3 inflammasome and increased sensitization to LPS-induced inflammasome activation in hepatocytes. In contrast, PUFA docosahexaenoic acid (DHA) had the potential to inhibit NLRP3 inflammasome expression in hepatocytes and partly abolished LPS-induced NLRP3 inflammasome activation. Furthermore, a high-fat diet increased but PUFA-enriched diet decreased sensitization to LPS-induced hepatic NLRP3 inflammasome activation in vivo. Moreover, PA increased but DHA decreased phosphorylated NF-κB p65 protein expression in hepatocytes.
Hepatic NLRP3 inflammasome activation played an important role in the development of non-alcoholic fatty liver disease. Dietary SFAs and PUFAs oppositely regulated the activity of NLRP3 inflammasome through direct activation or inhibition of NF-κB.
研究不同膳食脂肪酸对肝脏炎性小体激活的影响。
将野生型C57BL/6小鼠分为高脂饮食组或富含多不饱和脂肪酸(PUFA)饮食组。原代肝细胞分别用饱和脂肪酸(SFA)或PUFA处理,并联合脂多糖(LPS)。通过实时PCR和蛋白质免疫印迹法检测NOD样受体蛋白3(NLRP3)炎性小体、过氧化物酶体增殖物激活受体-γ和核因子-κB(NF-κB)的表达。检测半胱天冬酶-1的活性和白细胞介素-1β的产生。
高脂饮食诱导的肝脏脂肪变性足以诱导和激活肝脏NLRP3炎性小体。SFA棕榈酸(PA)直接激活NLRP3炎性小体,并增加肝细胞对LPS诱导的炎性小体激活的敏感性。相比之下,PUFA二十二碳六烯酸(DHA)有抑制肝细胞中NLRP3炎性小体表达的潜力,并部分消除LPS诱导的NLRP3炎性小体激活。此外,高脂饮食增加了体内对LPS诱导的肝脏NLRP3炎性小体激活的敏感性,但富含PUFA的饮食降低了这种敏感性。而且,PA增加但DHA降低了肝细胞中磷酸化NF-κB p65蛋白的表达。
肝脏NLRP3炎性小体激活在非酒精性脂肪性肝病的发生发展中起重要作用。膳食SFA和PUFA通过直接激活或抑制NF-κB对NLRP3炎性小体的活性发挥相反的调节作用。