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IL-4及CD40 mAb对肾小管上皮细胞RANTES表达的影响
引用本文:梁鸣,阳晓,许韩师,李幼姬,叶任高,孔庆喻,董秀清,余学清. IL-4及CD40 mAb对肾小管上皮细胞RANTES表达的影响[J]. 中国病理生理杂志, 2004, 20(6): 1021-1024
作者姓名:梁鸣  阳晓  许韩师  李幼姬  叶任高  孔庆喻  董秀清  余学清
作者单位:中山大学附属一院肾内科, 教育部肾脏病临床研究重点实验室, 广东 广州 510080
基金项目:国家自然科学基金资助项目 (No .9970 933,30 0 70 717)
摘    要:目的:观察小鼠肾小管上皮细胞(TEC)在IL-4及CD40激活状态下激活正常T细胞表达和分泌因子(RANTES)分泌的变化。方法:刺激原代培养的小鼠肾小管上皮细胞,检测RANTES的表达,流式细胞仪检测CD40表达。结果:(1)常规培养下,小鼠TEC可表达一定量的CD40,用IL-4刺激TEC 24 h,细胞表面CD40 MFI 显著高于对照组(P<0.01)。(2)常规培养下,小管上皮细胞仅分泌极少量的RANTES(14.78 ng/L±2.20 ng/L),在IL-4刺激或CD40mAb激活后TEC RANTES蛋白分泌分别为43.61±13.73和73.77±4.28,显著高于对照组(P<0.01)。用IL-4刺激肾小管细胞CD40表达的同时,加入纯化的CD40mAb激活CD40受体,TEC RANTES 的合成、分泌显著高于对照组(131.77±41.87,P<0.01),与单纯IL-4刺激组及CD40mAb刺激组比较差异显著(均P<0.01)。(3)用IL-4、CD40mAb及 IL-4+CD40mAb刺激TEC细胞24 h,各刺激组RANTES mRNA表达显著高于对照组(P<0.05)。结论:IL-4及CD40-CD40L共刺激信号可调控RANTES合成及分泌,参与TEC炎症过程。

关 键 词:小管上皮细胞  白细胞介素4  抗原  CD40  CD40配体  Th2细胞  
文章编号:1000-4718(2004)06-1021-04
收稿时间:2002-12-13
修稿时间:2003-03-27

Effect of IL-4,CD40L on RANTES production in murine renal tubular epithelial cells
LIANG Ming,YANG Xiao,XU Han-shi,LI You-ji,YE Ren-gao,KONG Qing-yu,DONG Xiu-qing,YU Xue-qing. Effect of IL-4,CD40L on RANTES production in murine renal tubular epithelial cells[J]. Chinese Journal of Pathophysiology, 2004, 20(6): 1021-1024
Authors:LIANG Ming  YANG Xiao  XU Han-shi  LI You-ji  YE Ren-gao  KONG Qing-yu  DONG Xiu-qing  YU Xue-qing
Affiliation:Department of Nephrology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China
Abstract:AIM: To investigate the effect of IL-4, CD40L on RANTES production in murine renal tubular epithelial cells (TEC). METHODS: TEC were obtained from mouse, expression of RANTES and CD40 on TEC were measured. RESULTS: (1) Activation of TEC with IL-4 resulted in significant increase in CD40 expression (P<0.01).(2) A little RANTES was detectable in supernatants without stimulation. TEC stimulated with either cytokine IL-4 or CD40mAb resulted in strong induction of RANTES production up to 43.61±13.73 or 73.77±4.28(ng/L), respectively. The differences of RANTES between two stimulation groups and that in medium were statistically significant (P<0.01). TEC stimulated with IL-4 and CD40mAb produced more RANTES than that in medium (P<0.01), which was higher than that with single stimulation (P<0.01). (3) TEC stimulated with IL-4 or CD40 activation or combined stimulation of IL-4 and CD40mAb resulted in increase in levels of RANTE mRNA, which were higher than that in medium. CONCLUSION: Co-stimulation of TEC by IL-4 and CD40mAb up-regulated the RANTES production, suggesting the RANTES may participate in the inflammation of TEC.
Keywords:Tubular epithelial cell  Interleukin-4  Antigens   CD40  CD40 ligand  Th2 cells
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