中国麻风皮肤病杂志 ›› 2018, Vol. 34 ›› Issue (8): 449-452.

• 论著 •    下一篇

mTORC1信号通路在狼疮鼠体内的表达及意义

谢双德1 魏姗姗2 张华年1 王桂松1 彭学标1 赵珂3 李俊灏1 赖宽   

  1. 1南方医科大学南方医院皮肤科,广州,510515 2南方医科大学珠江医院皮肤科,广州,510282 3南方医科大学南方医院血液科,广州,510515
  • 出版日期:2018-08-15 发布日期:2018-12-11
  • 通讯作者: 赖宽,E-mail:kuan_lai@163.com

The expression of mTORC1 pathway in murine model of systemic lupus erythematosus

XIE Shuangde1,WEI Shanshan2, ZHANG Huanian1, WANG Guisong1, PENG Xuebiao1, Zhao Ke3, LI Junhao1,LAI Kuan1   

  1. 1.Departmen of Dematology,Nanfang Hospital,Southern Medical University,Guangzhou 510515,China;2.Departmen of Dematology,Zhujiang Hospital,Southern Medical University,Guangzhou 510282,China;3.Department of Hematology,Nanfang Hospital,Southern Medical University,Guangzhou 510515, China
  • Online:2018-08-15 Published:2018-12-11
  • Contact: LAI Kuan, E-mail:kuan_lai@163.com

摘要: 目的:检测mTORC1信号通路在系统性红斑狼疮鼠体内的表达,探讨其在系统性红斑狼疮发病中的作用。方法: 研究对象为6只B6.MRL/lpr狼疮小鼠和6只C57正常小鼠。RT-PCR和Western blot检测肾脏组织Akt、mTOR、p70S6K、IL-17 mRNA和蛋白的表达。细胞内染色流式细胞术检测脾脏Th17淋巴细胞亚群比例。结果: 狼疮鼠组Akt、mTOR、p70S6K、IL-17 mRNA、磷酸化蛋白表达水平高于对照组(P<0.05);狼疮鼠组的Th17细胞占CD4+T细胞的比例高于正常对照组(P<0.05)。结论: mTORC1(Akt-mTOR-p70S6K)信号通路在SLE的发病中起着重要作用。

关键词: 系统性红斑狼疮, mTOR, p70S6K, Th17

Abstract: Objective: To detect the level of mTORC1 pathway related factors in the murine model of systemic lupus erythematosus (SLE) and to explore its effect in the development of SLE. Methods: There were 6 B6.MRL/lpr lupus mice in the experimental group and 6 C57 mice in the control group. The levels of Akt, mTOR, p70S6K, IL-17 mRNA and protein in kidney were detected by RT-PCR and western blot. The percentage of Th17 lymphocytes in CD4+T cells in spleen was detected by flow cytometry. Results: The mRNA and phosphoprotein of Akt, mTOR, p70S6K and IL-17 in the experimental group were higher than those in the control group. The percentage of Th17 lymphocytes in CD4+T cells in the experimental group was higher than that in the control group. Conclusion: The activation of mTORC1(Akt-mTOR-p70S6K) pathway may play an important role in the development of SLE.

Key words: systemic lupus erythematosus, mTOR, p70S6K, Th17