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研究报告: 实验性自身免疫性葡萄膜炎模型中肝脏免疫系统紊乱的研究
引用本文:林玮,宋楠楠,王贝贝,毕宏生.研究报告: 实验性自身免疫性葡萄膜炎模型中肝脏免疫系统紊乱的研究[J].生物化学与生物物理进展,2017,44(12):1083-1094.
作者姓名:林玮  宋楠楠  王贝贝  毕宏生
作者单位:山东中医药大学眼科所,济南 250002;山东省医科院基础医学研究所微生物室,济南 250062,山东省医科院基础医学研究所微生物室,济南 250062,山东中医药大学眼科所,济南 250002,山东中医药大学眼科所,济南 250002
基金项目:国家自然科学基金(81500710),山东省自然科学基金(ZR2013HQ039),山东省医药卫生科技发展计划项目(2015WS0194),山东省医学科学院院级科技计划(2015-25)和山东省医学科学院创新项目资助
摘    要:葡萄膜炎是一种反复发作的炎症性疾病,可导致免疫系统功能障碍和多器官损伤.然而,葡萄膜炎是否导致肝功能损害尚不十分清楚.本文通过运用流式分析技术和激光共聚焦成像技术,研究了实验性自身免疫葡萄膜炎模型的肝脏病理和功能变化.结果显示肝损伤可出现在葡萄膜炎的炎症后期并与眼损伤程度相关.并且CD3+ CD4+ T细胞、CD3- NK1.1+ DX5- NK细胞、和CD11b+ F4/80- ly6c+ 细胞在感染的眼睛和肝脏中增加.将CD3+ CD4+ T细胞回输给炎症的小鼠后,眼睛和肝脏的病理损伤加重.此外,在炎症的小鼠中可见血管扩张,大量淋巴细胞浸润到炎症的眼和肝脏的血管周围.总之,我们的研究结果提示,肝损伤可以发生在小鼠葡萄膜炎模型中,这种损伤可能与通过外周循环浸润到肝脏的CD3+ CD4+ T细胞有关.

关 键 词:T细胞,葡萄膜炎,肝损伤,血循环
收稿时间:2017/7/23 0:00:00
修稿时间:2017/9/7 0:00:00

Research Papers: A Disorder of The Liver Immune System in Experimental Autoimmune Uveitis
LIN Wei,SONG Nan-Nan,Wang Bei-Bei and BI Hong-Sheng.Research Papers: A Disorder of The Liver Immune System in Experimental Autoimmune Uveitis[J].Progress In Biochemistry and Biophysics,2017,44(12):1083-1094.
Authors:LIN Wei  SONG Nan-Nan  Wang Bei-Bei and BI Hong-Sheng
Institution:Eye Institute of Shandong University of Traditional Chinese Medicine, Jinan 250002, China; Department of Microbiology, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan 250062, China,Department of Microbiology, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan 250062, China,Eye Institute of Shandong University of Traditional Chinese Medicine, Jinan 250002, China and Eye Institute of Shandong University of Traditional Chinese Medicine, Jinan 250002, China
Abstract:Uveitis is a recurrent inflammatory disease that can lead to immune system dysfunction and multiple organ injuries. However, whether uveitis causes liver functional damage is still unclear. Herein, by using flow cytometry and confocal, we investigated the pathological and functional changes of liver in an experimental autoimmune model of uveitis (EAU). Hepatic damage was observed at the inflammatory stage of uveitis and was associated with severity of eye damage. Moreover, the expression of CD3+CD4+ T cells, CD3-NK1.1+DX5- NK cells, and CD11b+F4/80-Ly6c+ cells were increased in the inflamed eye and liver. Furthermore, the pathological damage of EAU and hepatic impairment were aggravated after transferring CD3+CD4+ T cells into EAU mice. Additionally, vascular dilation and infiltration of CD3+CD4+ T cells were found in the eyes and livers of EAU mice. In conclusion, our findings suggest that liver injury could occur in EAU. This liver injury may be associated with increased CD3+CD4+ T cells, which may infiltrate into liver through circulatory system.
Keywords:T cells  experimental autoimmune uveitis  liver immunity  blood circulation
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