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Foxp3+Tregs 在慢性间歇低氧所致肝损伤中的作用
引用本文:白晓纯 王琳 赵忺 田建立. Foxp3+Tregs 在慢性间歇低氧所致肝损伤中的作用[J]. 天津医药, 2016, 44(6): 712-715. DOI: 10.11958/20150217
作者姓名:白晓纯 王琳 赵忺 田建立
作者单位:1天津医科大学总医院保健医疗部 (老年病科), 天津市老年病学研究所 (邮编300052); 2天津市西青医院
基金项目:天津市自然科学基金资助项目 (11JCYBJC28300); 天津市卫生局科技基金 (2014KZ119)
摘    要:摘要:目的 探讨叉头样转录因子 P3(Foxp3)阳性调节性 T 细胞(Tregs)在慢性间歇低氧诱导的肝损伤中的作用。方法 32 只雄性 Wistar 大鼠随机均分为空白对照组(A 组)、 高脂饮食组(B 组)、 间歇低氧组(C 组)和高脂饮食+间歇低氧组 (D 组)。实验暴露 4 周后留取血标本并分离出肝组织, 采用全自动分析仪检测各组大鼠血总胆固醇(TC)、 低密度脂蛋白胆固醇(LDL-C)、 丙氨酸转氨酶(ALT)、 天冬氨酸转氨酶(AST)的水平, 比色法测定肝组织丙二醛 (MDA) 含量, 放射免疫法检测促炎症细胞因子肿瘤坏死因子 (TNF) -α和白细胞介素 (IL) -1β水平, Western blot 法检测肝组织 Foxp3 蛋白表达。结果 各组 TC、 LDL-C 比较均是 B 组高于 A、 C、 D 组, D 组高于 A、 C 组 (均 P<0.05),而 A 组与 C 组差异无统计学意义。ALT、 AST、 MDA、 TNF-α、 IL-1β水平比较均是 C 组高于 A 组, D 组高于 A、 B、 C 组(均 P<0.05), 而 A 组与 B 组、 B 组与 C 组间差异均无统计学意义。D 组肝组织 Foxp3 蛋白表达水平明显低于其他各组 (P<0.05)。结论 Foxp3+Tregs 参与在高脂饮食基础上慢性间歇低氧所致的肝损伤的调节, 在此过程中可能起重要的保护性免疫作用。

关 键 词:叉头转录因子类  慢性间歇低氧  非酒精性脂肪性肝病  氧化应激  炎症反应   Foxp3+Tregs  
收稿时间:2015-10-13
修稿时间:2015-12-23

The role of Foxp3+T cells in chronic intermittent hypoxia induced liver injury
BAI Xiaochun,WANG Lin,ZHAO Xian,TIAN Jianli. The role of Foxp3+T cells in chronic intermittent hypoxia induced liver injury[J]. Tianjin Medical Journal, 2016, 44(6): 712-715. DOI: 10.11958/20150217
Authors:BAI Xiaochun  WANG Lin  ZHAO Xian  TIAN Jianli
Affiliation:1 Department of Geriatrics, Tianjin Medical University General Hospital,Tianjin Geriatrics Institute, Tianjin 300052, China; 2 Tianjin Xiqing Hospital
Abstract:Abstract: Objective To explore the role of Foxp3 + T cells (Tregs) in liver injury induced by chronic intermittent hypoxia. Methods Thirty-two male Wister rats were divided into four groups: control group (A), high-fat diet group (B), intermittent hypoxia group (C), and high- fat diet and intermittent hypoxia group (D). After 4 weeks, blood samples were collected and livers were surgically removed. Using the standard automatic clinical analyzer to test serum levels of total cholesterol (TC), low density lipoprotein cholesterol (LDL- C), alanina aminotransferase (ALT) and aspartato aminotransferase (AST). The MDA content of liver tissue was measured by colorimetrc method. The levels of TNF-α and IL- 1β were measured by radiommunoassay, and the expression of Foxp3 protein was measured by Western blotting technique. Results Serum levels of TC and LDL-C were significantly higher in B group than those of A, C and D groups, and which were higher in D group than those of A and C groups (P<0.05). There were no significant differences in serum levels of TC and LDL-C between A group and C group. Serum levels of ALT, AST, MDA, TNF-α and IL-1β were significantly higher in C group than those of A group, and which were significantly higher in D group than those of A, B and C groups (P<0.05). There were no significant differences in these indicators between A group and B group, and between B group and C group. Foxp3 protein expression in liver was significantly lower in D group than that of other groups (P<0.05). Conclusion Foxp3+ T regulatory cells involve in the regulation of hepatic injury induced by chronic intermittent hypoxia on the basis of a high-fat diet, and which may play an important role in this process of protective immune response.
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