Csak Timea, Pillai Arun, Ganz Michal, Lippai Dora, Petrasek Jan, Park Jin-Kyu, Kodys Karen, Dolganiuc Angela, Kurt-Jones Evelyn A, Szabo Gyongyi
Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Liver Int. 2014 Oct;34(9):1402-13. doi: 10.1111/liv.12537. Epub 2014 Apr 17.
BACKGROUND & AIMS: Inflammation promotes the progression of non-alcoholic steatohepatitis (NASH). Toll-like receptor 4 (TLR4) and TLR9 activation through myeloid differentiation primary response gene 88 (MyD88) and production of mature interleukin-1β (IL-1β) via inflammasome activation contribute to steatohepatitis. Here, we investigated the inter-relationship between TLR signalling and inflammasome activation in dietary steatohepatitis.
Wild type (WT), TLR4- and MyD88-deficient (KO) mice received methionine-choline-deficient (MCD) or -supplemented (MCS) diets for 5 weeks and a subset was challenged with TLR9 ligand CpG-DNA.
TLR4, TLR9, AIM2 (absent in melanoma 2) and NLRP3 (NLR family pyrin domain containing 3) inflammasome mRNA, and mature IL-1β protein levels were increased in MCD diet-induced steatohepatitis compared to MCS controls. TLR9 stimulation resulted in greater up-regulation of the DNA-sensing AIM2 expression and IL-1β production in livers of MCD compared to MCS diet-fed mice. High mobility group box 1 (HMGB1), a TLR9-activating danger molecule and phospho-HMGB1 protein levels were also increased in livers of MCD diet-fed mice. MyD88- but not TLR4-deficiency prevented up-regulation of AIM2, NLRP3 mRNA and IL-1β protein production in dietary steatohepatitis. Selective MyD88 deficiency either in bone marrow (BM)-derived or non-BM-derived cells attenuated hepatic up-regulation of inflammasome mRNA, caspase-1 activation and IL-1β protein production, but only BM-derived cell-specific MyD88-deficiency attenuated liver injury.
Our data demonstrate that both bone marrow-derived and non-BM-derived cells contribute to inflammasome activation in a MyD88-dependent manner in dietary steatohepatitis. We show that AIM2 inflammasome expression and activation are further augmented by TLR9 ligands in dietary steatohepatitis.
炎症促进非酒精性脂肪性肝炎(NASH)的进展。通过髓样分化初级反应基因88(MyD88)激活Toll样受体4(TLR4)和TLR9以及经由炎性小体激活产生成熟白细胞介素-1β(IL-1β),均参与脂肪性肝炎的发生。在此,我们研究了饮食性脂肪性肝炎中TLR信号传导与炎性小体激活之间的相互关系。
野生型(WT)、TLR4缺陷型和MyD88缺陷型(KO)小鼠接受蛋氨酸-胆碱缺乏(MCD)或补充蛋氨酸-胆碱(MCS)的饮食5周,其中一部分用TLR9配体CpG-DNA进行攻击。
与MCS对照组相比,MCD饮食诱导的脂肪性肝炎中TLR4、TLR9、黑色素瘤缺乏因子2(AIM2)和含NLR家族pyrin结构域3(NLRP3)炎性小体的mRNA以及成熟IL-1β蛋白水平升高。与MCS饮食喂养的小鼠相比,TLR9刺激导致MCD饮食喂养小鼠肝脏中DNA感应AIM2表达和IL-1β产生的上调幅度更大。高迁移率族蛋白B1(HMGB1),一种激活TLR9的危险分子,以及磷酸化HMGB1蛋白水平在MCD饮食喂养小鼠的肝脏中也升高。MyD88缺陷而非TLR4缺陷可阻止饮食性脂肪性肝炎中AIM2、NLRP3 mRNA和IL-1β蛋白产生的上调。骨髓(BM)来源或非BM来源细胞中的选择性MyD88缺陷可减弱炎性小体mRNA的肝脏上调、半胱天冬酶-1激活和IL-1β蛋白产生,但只有BM来源细胞特异性MyD88缺陷可减轻肝损伤。
我们的数据表明,在饮食性脂肪性肝炎中,BM来源和非BM来源的细胞均以MyD88依赖的方式促成炎性小体激活。我们表明,在饮食性脂肪性肝炎中,TLR9配体可进一步增强AIM2炎性小体的表达和激活。