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特异性细胞因子对T辅助17细胞和T调节性细胞表达的调节作用
引用本文:俞秋兴,唐军,颜茹红,朱雪明,顾爱萍.特异性细胞因子对T辅助17细胞和T调节性细胞表达的调节作用[J].中华检验医学杂志,2009,32(4).
作者姓名:俞秋兴  唐军  颜茹红  朱雪明  顾爱萍
作者单位:1. 苏州大学第二临床医学院医学检验系,215004
2. 苏州大学第二临床医学院医学核医学科,215004
摘    要:目的 探讨多种细胞因子包括转化生长因子β(TGF-β)、白细胞介素6(IL-6)、白细胞介素2(IL-2)对CD+4T淋巴细胞的分化调节作用.方法 将人外周血T淋巴细胞、鼠脾脏T淋巴细胞在不同的刺激条件下进行体外培养,采用流式细胞仪分析活化T淋巴细胞中CD+4IL-17+T辅助17细胞(Th17细胞)、C+4IL-17+T淋巴细胞、CD+4CD+25FOXP+3T调节性细胞(Treg细胞)的表达情况.结果 鼠脾脏T淋巴细胞培养液中有TGF-β存在时可促进Treg细胞、rh17细胞和CD+8;IL-17+T淋巴细胞分化,表达水平分别为(7.8±2.2)%、(12.6±3.1)%、(10.1±2.6)%.无细胞因子培养的同类细胞为实验对照组,表达水平分别为(4.8±0.6)%、(1.7±0.5)%、(1.0±0.4)%,差异均有统计学意义(q=4.09、8.80、9.61,P<0.05或P<0.01).TGF-β与IL-6细胞因子共同存在时可促进Th17和CD+8IL-17+T淋巴细胞分化,表达水平分别为(17.8±5.3)%、(15.0±4.2)%,而分化受抑制的Treg细胞的表达水平为(4.I±1.2)%,与TGF-β组同类细胞表达水平比较差异均有统计学意义(q=5.03、5.17、5.04,P均<0.01).在TGF-β刺激的T淋巴细胞中加入IL-2细胞因子可使Th17细胞、CD+8;IL-17+T淋巴细胞表达减少,同时伴有Treg细胞表达量的增加;在加入抗IL-2后结果相反,即Th17细胞、CD+8IL-17+T淋巴细胞表达水平增加,Treg细胞表达水平减少.人外周血T淋巴细胞上Th17、CD+8IL-17+、Treg细胞表达水平变化趋势与鼠脾脏淋巴细胞相似.结论 不同细胞因子对于调控Th17细胞和Treg细胞之间的平衡起着十分重要的作用.

关 键 词:细胞因子类  T淋巴细胞  辅助诱导  T淋巴细胞  调节性

Regulative role of specific cytokine on expression of T-helper 17 cells and regulatory T cells
YU Qiu-xing,TANG Jun,YAN Ru-hong,ZHU Xue-ming,GU Ai-ping.Regulative role of specific cytokine on expression of T-helper 17 cells and regulatory T cells[J].Chinese Journal of Laboratory Medicine,2009,32(4).
Authors:YU Qiu-xing  TANG Jun  YAN Ru-hong  ZHU Xue-ming  GU Ai-ping
Abstract:Objective To investigate the roles of a variety of cytokines including transforming growth factor beta (TGF-β),interleukin-6 (IL-6) and interleukin-2 (IL-2) in the differentiation of CD+4 Tlymphocyte cells.Methods T lymphocyte cells either in human peripheral blood or routine spleen were cultured in vitro under different stimulation conditions.Flow cytometry was used to analyze the percentages of CD+4IL-17+ T-helper 17(Th17) cells,CD+8 IL-17+ T cells,CD+4 CD+25 FOXP+3 T regulatory (Treg) cells among activated T cells.Results Differentiation of Treg cells,Th17 cells and CD+8 IL-17+ T lymphocyte cells was enhanced when murine splenic T cells were cultured with TGF-β.The levels of expression were (7.8±2.2)%,(12.6±3.1)%,(10.1±2.6)% ,respectively.Experimental control group was severally same type of T cells without cytokine treatment.The levels of expression were (4.8±0.6) %,(1.7±0.5) %,(1.0±0.4) %,respectively.There were statistically significant differences among them (q=4.09,8.80,9.61.P<0.05 or P<0.01).Under combination treatment with IL-6 and TGF-β,(17.8±5.3) % Th17 cells and (15.0±4.2)% CDCD+8 IL-17CD+ T cells were induced,whereas the levels of Treg cells whose differentiation were restrained were (4.1±1.2) %.The differences were statistically significant compared with the level of same type of T cells in TGF-β group (q=5.03,5.17,5.04,P<0.01).Moreover,combination treatment with IL-2 and TGF-β decreased percentages of Th17 and CDCD+8 IL-17CD+ T cells and increased percentages of Treg cells in T cell population.There was an opposite effect when anti-IL-2 was apphed.The percentages of Th17 and CD+8 IL-17+ T cells were increased and the percentages of Treg cells were reduced The regulation trend of T lymphocyte cells in human peripheral blood was similar with those in routine spleen.Conclusion Various cytokines are of great importance in the regulation of the balance between Th17 and Treg cell.
Keywords:Cytokines  T-lymphocytes  helper-inducer  T-lymphocytes  regulatory
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