检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:姜晓峰[1] 朱磊[1] 崔哲铭[1] 郭大伟[1] 孙文郁[1] 林琳[1] 王学范[1] 唐裕福[1] 梁健[1]
出 处:《中华器官移植杂志》2011年第4期245-248,共4页Chinese Journal of Organ Transplantation
基 金:教育部留学回国人员科研启动基金(08-890);辽宁省教育厅基金(2008824)
摘 要:目的研究CXC趋化因子受体6(CXCR6)在同种异体小鼠心脏移植中的表达及CXC趋化因子配体16(CXCL16)与CXCR6相互作用对移植物存活时间的影响。方法以野生型Balb/c小鼠(H-2^d)为供者(同种移植组),或以野生型C57BL/6小鼠(H-2^b)为供者(同系移植组),以野生型C57BL/6小鼠为受者分别行小鼠腹腔异位心脏移植。测定同系和同种移植组小鼠移植心脏CXCR6mRNA的表达,并测定受者脾脏CD8^+T淋巴细胞CXCR6的表达。另制作小鼠同种异位心脏移植模型(Balb/c小鼠为供者,C57BL/6小鼠为受者),将其分为实验组和对照组,实验组受者移植当天至发生排斥反应时腹腔注射抗CXCL16抗体,对照组受者同期注射对照抗体。记录两组移植心脏存活时间。进行CD8^+T淋巴细胞的细胞毒试验,即用Balb/c小鼠脾细胞免疫C57BL/6小鼠后,获取C57BL/6小鼠脾脏CD8^+T淋巴细胞,将Balb/c小鼠脾细胞与C57BL/6小鼠CD8^+T淋巴细胞混合培养,分别加入抗CXCL16抗体、小鼠IgG(对照抗体)和抗CINOL抗体。结果同种移植组移植心脏中CXCR6mRNA的表达以及脾脏CD8^+T淋巴细胞上CXCR6的表达均高于同系移植组和正常对照组。抗CXCL16抗体对CD8^+T淋巴细胞的细胞毒活性无影响。与对照组相比较,实验组小鼠移植心脏存活时间并未明显延长。结论小鼠心脏移植排斥反应中CD8^+T淋巴细胞CXCR6的表达上升,阻断CXCL16/CXCR6相互作用并不能延长移植心脏的存活时间。Objective To investigate the expression of CXCR6 in allograft rejection and effect of CXCL16/CXCR6 interaction on allograft survival. Methods Intra-abdominal heterotopic heart transplantation was performed using wild type (WT) Balb/c mice (H-2d) (allogeneic)as donors or WT C57BL/6 mice (B6, H-2^b) (syngeneic) as donors, and using WT B6 mice as recipients. The intragraft expression of CXCR6 and expression of CXCR6 in CD8^+ T cells of the spleens from syngeneic and allogeneic recipients were examined. The allogeneic recipients were further divided into the experimental group (n = 5) and control group (n = 6) randomly. The experiment group and control group were injected with anti-CXCL16 mAb or control mAb respectively until rejection occurred. The cardiac allograft survival in experimental group and control group was evaluated. Results Rejected allografts showed higher expression of CXCR6 than syngeneic cardiac grafts. More importantly, expression of CXCR6 in CD8^+ T cells was also up-regulated by allograft rejection. However, injection of anti-CXCL16 mAb could not inhibit cytotoxic activity of CD8^+ T cells. Moreover, experimental group could not prolong the cardiac graft survival time as compared with control group. Conclusion Expression of CXCR6 in CD8^+T cells is up-regulated in allograft rejection.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.15