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国家自然科学基金(30700792)

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Hyaluronic acid fragments evoke Kupffer cells via TLR4 signaling pathway被引量:33
2009年
Kupffer cells, expressing toll-like receptor 4 (TLR4), play a central role in hepatic ischemia/reperfusion (I/R) injury. Hyaluronic acid (HA) fragments, degradative products of high-molecular-weight HA (HMW-HA), acquire the ability to activate immune cells under inflammatory conditions. Here we inves- tigated whether HA fragments could activate Kupffer cells and analyzed the underlying mechanism. Kupffer cells were isolated from wild-type mice (WT, C3H/HeN) and TLR4 mutant mice (C3H/HeJ) and HA fragments were produced by the methods of enzyme digestion and chromatography. Then Kupffer cells were stimulated by HA fragments or other control stimuli. The activation of Kupffer cells was estimated as the release of pro-inflammatory cytokines. The activation of p38 MAPK pathway of Kupffer cells was checked and blocking experiments were done as well. The results indicated that HA fragments acquired the ability to activate Kupffer cells in vitro, which was TLR4 dependent and not due to contamination of lipopolysaccharide. Experiments of p38 MAPK kinase inhibition by SB-203580 verified p38 MAPK was required in HA fragments induced Kupffer cells activation. This suggests that HA fragments, degradative products of one of the major glycosaminoglycans of the extracellular matrix, play critical roles in Kupffer cell activation mediated by TLR4 signaling pathway, which is, at least partially, de- pendent on p38 MAPK activation.
ZHANG JinXiang1, WANG Hui2, XIAO Qing3, LIANG HuiFang4, LI ZhuoYa4, JIANG ChunFang1, WU HeShui5 & ZHENG QiChang5 1 Department of Emergency Surgery, Union Hospital Affiliated to Huazhong University of Science and Technology, Wuhan 430022, China 2 Department of Medical Genetics, Tongji Medical College Affiliated to Huazhong University of Science and Technology, Wuhan 430030, China 3 Department of Ophthalmology, Union Hospital Affiliated to Huazhong University of Science and Technology, Wuhan 430022, China 4 Department of Medical Immunology, Tongji Medical College Affiliated to Huazhong University of Science and Technology, Wuhan 430030, China 5 Department of General Surgery, Union Hospital Affiliated to Huazhong University of Science and Technology, Wuhan 430022, China
关键词:KUPFFERFRAGMENTSTOLL-LIKEP38MAPKREPERFUSION
低分子量透明质酸片段通过toll样受体4信号途径激活枯否细胞被引量:2
2008年
高分子量透明质酸(high-molecular-weight hyaluronic acid,HMW-HA)是重要的肝脏基质,分子量高达2×106Da以上,可被活性氧分子(reactive oxygen species,ROS)等降解成低分子量透明质酸片段(hyaluronic acid fragments,HA fragments),后者能被toll样受体4(toll-like receptor4,TLR4)识别并激活免疫细胞诱发炎症反应.基于枯否细胞表达TLR4,推测HA fragments通过激活枯否细胞TLR4信号系统而启动肝脏缺血再灌注损伤.从TLR4基因突变型(C3H/HeJ,TLR4Mut/Mut)及野生型(C3H/HeN,TLR4+/+)小鼠分离肝脏枯否细胞常规培养,用酶降解及色谱柱分离方法制备HA fragments,观察HMW-HA及HA fragments激活枯否细胞的差异,检测培养上清肿瘤坏死因子-α或白介素-1β水平变化;枯否细胞p38MAPK信号通路的活化;用特异性p38MAPK阻断剂--SB-203580,阻断p38MAPK活化后,观察培养上清中肿瘤坏死因子-α或白介素-1β水平变化.结果显示HA fragments可以促进TLR4+/+枯否细胞分泌促炎因子,不能诱导TLR4Mut/Mut枯否细胞分泌促炎因子.而HMW-HA既不能促进TLR4+/+枯否细胞也不能促进TLR4Mut/Mut枯否细胞分泌促炎因子.采用多黏菌素中和脂多糖后,HA fragments促进TLR4+/+枯否细胞分泌促炎因子的能力不变,这一过程伴随p38MAPK信号通路的活化.当运用p38MAPK信号通路的特异性阻断剂SB-203580,抑制p38MAPK活性时,HA fragments促进TLR4+/+枯否细胞分泌促炎因子的能力显著下降.因此与基质组成成分HMW-HA不同,HA fragments可以通过TLR4激活枯否细胞,促进其分泌促炎因子诱发炎症反应,这一过程依赖于p38MAPK的激活.
张进祥王慧肖青梁慧芳李卓娅蒋春舫吴河水郑启昌
关键词:枯否细胞TOLL样受体4P38MAPK脂多糖缺血再灌注损伤
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