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作 者:韩澍[1] 朱有华[1] 王立明[1] 曾力[1] 傅尚希[1] 郑鳕洋[1]
机构地区:[1]第二军医大学附属长征医院全军器官移植研究所,上海200003
出 处:《中华器官移植杂志》2014年第5期295-299,共5页Chinese Journal of Organ Transplantation
基 金:上海市自然科学基金(11ZR1448800)
摘 要:目的研究小鼠心脏移植排斥反应中小分子RNA494(miR-494)与辅助性T淋巴细胞17(TH17细胞)分化的相关性。方法分别建立颈部异位心脏移植模型:对照组,供者和受者均为C57BL/6小鼠;实验组,供者为Balb/c小鼠,受者为C57BL/6小鼠。利用逆转录聚合酶链反应(RT-PCR)检测移植物中miR-494与IL-17AmRNA的表达。分离移植物中CD4^+T淋巴细胞、CD8^+T淋巴细胞及CD45^+细胞,检测各组细胞中miR-494与IL-17AmRNA的表达。体外分离C57BL/6小鼠脾细胞,利用免疫磁珠法进行CD4^+T淋巴细胞分选,定向分化为TH1、TH2、TH17和调节性T淋巴细胞(Treg细胞)亚群,采用RT-PCR检测各细胞亚群IL-17AmRNA及miR-494的表达。结果小鼠心脏移植术后7d,实验组移植物中IL-17AmRNA表达高于对照组,而miR-494的表达低于对照组(均P〈0.05)。移植物CD4^+T淋巴细胞IL-17A mRNA表达高于对照组,而miR-494的表达降低(均P〈0.05)。体外培养TH17细胞亚群中,miR-494的表达显著低于Tn1、TH2和Treg细胞。结论miR-494可能与移植排斥反应中TH17细胞分化密切相关,miR-494可能通过调控TH17细胞在移植排斥反应中发挥作用。Objective To investigate correlation between microRNA (miR-494) and TH 17 cell differentiation in murine cervical heterotopic cardiac transplant model. Method The heterotopic cardiac transplant models of Balb/c→C57BL/6 mice were established as experimental group, and those of C57BL/6→C57BL/6 mice as control group. Real timepolymerase chain reaction(PCR) was used to detect miR-494 and interleukin(IL)-17A mRNA expression in the grafts. CD4^+ T cells, CD8^+ T cells and CD45^+ myeloid cells were isolated from the grafts, and miR-494 and IL-17 mRNA expression was detected. In vitro, lymphocytes in the spleen from C57BL/6 mice were harvested, and CD4^+ T cells were isolated with MACS and then stimulated to TH 1, TH2, TH 17, Treg subset cells. The expression of IL-17A mRNA and miR-494 in different T subsets was examined by Reverse transcription-polymerase chain reaction (RT-PCR). Result Two grafts from each study group were harvested on the 7th day post-transplantation. In experimental group, the IL-17A mRNA expression was increased, while the expression of miR-494 was decreased as compared with control group with the difference being significant between two groups. The expression of IL-17A mRNA in CD4^+ T cells of the grafts was significantly increased, while that expression of miR-494 was decreased. In vitro, the expression of miR-494 in TH 17 cells was significantly lower than that in TH 1, TH2 and Treg cells. Conclusion miR-494 is related closely to TH 17 cells differentiation in the transplant rejection, which may play a role in transplant rejection through regulating T. 17 ceils.
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