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实验性自身免疫性葡萄膜炎小鼠发病中Tim-3的表达及其作用

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目的 探讨T细胞免疫球蛋白黏蛋白分子-3(Tim-3)在实验性自身免疫性葡萄膜炎(EAU)发病中的表达和作用.方法 选取4~5周龄雄性C57BL/6J小鼠共12只;采用随机数字表法将12只小鼠分为对照组(3只)和实验组(9只).对照组(造模时间节点为造模后0 d)不做任何处理,实验组小鼠诱导建立EAU模型(按造模时间节点分为造模后7 d、14 d、21 d三个小组,每组3只小鼠).将光感受器间维生素A类结合蛋白651-670和完全弗氏佐剂充分混合乳化后,在实验组小鼠的双侧大腿、尾根部及颈后部皮下注射配制好的免疫乳剂(每只注射200 μL免疫乳剂,含500 µg光感受器间维生素A类结合蛋白651-670),随后实验组每只小鼠腹腔注射1 µg百日咳毒素.通过裂隙灯显微镜观察各组小鼠眼前节及眼底表现并采集图像.根据炎症程度采用Caspi分级标准对小鼠行临床评分及组织病理学评分.ELISA法检测小鼠血清中IFN-γ、IL-17的表达;实时荧光定量PCR法检测小鼠脾脏及眼球组织中Tim-3 mRNA的表达;Western blot法检测Tim-3蛋白的表达;免疫组织化学法检测脾脏组织Tim-3蛋白的表达.采用Graphpad Prism 9.0统计软件进行数据分析.结果 造模后小鼠的眼前节临床评分、眼底临床评分、组织病理学评分均随造模后时间的延长呈升高趋势,各组间的评分差异均有统计学意义(均为P<0.05).造模后小鼠血清中IFN-γ、IL-17的表达量均随造模后时间的延长呈升高趋势,且各组间的差异均有统计学意义(均为P<0.05).造模后小鼠脾脏与眼球组织中Tim-3 mRNA的相对表达量均随造模后时间的延长呈下降趋势,且各组间的差异均有统计学意义(均为P<0.05).小鼠眼球和脾脏组织中Tim-3蛋白的表达情况和mRNA相同.结论 Tim-3在EAU发病进程中的表达随着炎症的加重呈下调趋势,Tim-3在葡萄膜炎发病进程中可能发挥着负性免疫调控作用.
Expression and role of Tim-3 in the pathogenesis of experimental autoimmune uveitis
Objective To investigate the expression and role of T cell immunoglobulin and mucin domain-containing protein 3(Tim-3)in the pathogenesis of experimental autoimmune uveitis(EAU).Methods A total of 12 male C57BL/6J mice,aged 4 to 5 weeks,were selected and divided into the control group(n=3)and the experimental group(n=9)using a random number table.The control group(modeling time point:0 days after modeling)received no treatment,while the experimental group was induced to establish an EAU model(divided into three subgroups according to the modeling time points:7 days,14 days,and 21 days after modeling,with 3 mice in each subgroup).Firstly,the interphotoreceptor retinoid-binding protein 651-670 and complete Freund's adjuvant were fully mixed and emulsified.Then,the emulsion was subcutaneously injected into the two thighs,tail base,and neck of mice in the experimental group(each mouse received 200 µL of immune emulsion containing 500 pg of interphotoreceptor retinoid-binding protein 651-670).Subsequently,each mouse in the experimental group was also intraperitoneally injected with 1 µg of pertussis toxin.The anterior segment and fundus of mice in each group were observed and photographed under a slit-lamp microscope.The clinical and histopatho-logical scoring of these mice was conducted according to the Caspi grading scale based on the severity of inflammation.The serum levels of IFN-γ and IL-17 were measured using the enzyme-linked immunosorbent assay(ELISA),while the mRNA expression of Tim-3 in the spleen and ocular tissues was detected using the real-time quantitative polymerase chain reaction(RT-qPCR).Western blot was employed to detect the protein expression of Tim-3,and immunohistochemistry was used to examine the protein expression of Tim-3 in the spleen tissue.Statistical analysis was performed using GraphPad Prism 9.0.Results The clinical scores of the anterior segment,fundus,and histopathology of the mice increased over time after modeling,with statistically significant differences among these groups(P<0.05).The serum levels of IFN-γ and IL-17 in the mice also increased over time after modeling,with statistically significant differences among these groups(P<0.05).The relative mRNA expression of Tim-3 in the spleen and ocular tissues of the mice decreased over time after modeling,with statistically significant differences among these groups(P<0.05).The protein expression of Tim-3 in the ocular and spleen tissues showed the same pattern as its mRNA expression.Conclusion The expression of Tim-3 decreases with the exacerbation of inflammation in the progression of EAU,suggesting that Tim-3 may play a negative immunoregulatory role in the development of uveitis.

experimental autoimmune uveitisautoimmune diseaseTim-3interferon gammainterleukin

吴雄飞、张秋瑾、郑柳、杨彬彬、李金清、丁芝祥

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541000 广西壮族自治区桂林市,桂林医学院

541000 广西壮族自治区桂林市,桂林医学院附属医院眼科

实验性自身免疫性葡萄膜炎 自身免疫性疾病 Tim-3 干扰素-γ 白细胞介素

2025

眼科新进展
新乡医学院

眼科新进展

北大核心
影响因子:0.961
ISSN:1003-5141
年,卷(期):2025.45(1)