• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[CXCL9和CXCL10在小鼠再次移植后急性排斥反应中的作用]

[Roles of CXCL9 and CXCL10 in acute rejection after retransplantation in mice].

作者信息

Zhuang Jiawei, Shan Zhonggui, Ma Teng, Zhou Xiaobiao, Qiu Shuiwei

机构信息

Department of Cardiac Surgery, First Affliated Hospital,Xiamen University, Xiamen 361003, China.

Department of Cardiac Surgery, First Affliated Hospital,Xiamen University, Xiamen 361003, China. Email:

出版信息

Zhonghua Yi Xue Za Zhi. 2014 May 27;94(20):1584-6.

PMID:25146751
Abstract

OBJECTIVE

To observe the effects of chemokines CXCL9 and CXCL10 on cardiac allograft acute rejection mediated by alloreactive memory T cells in a retransplantation model.

METHODS

Heart transplantation was performed 6 weeks after skin grafting. The mice were divided into 3 groups of control (direct heterotopic heart transplantation without skin grafting); experimental (heart transplantation after skin grafting) and syngraft (C57BL/6→C57BL/6, heterotopic heart transplantation) (n = 12 each). Graft survival and the pathological changes of cardiac graft were observed. And related gene expression in cardiac grafts and serum concentration of CXCL9/CXCL10 were detected.

RESULTS

The mean survival time of control and experimental groups was 7.75 and 3.25 days respectively (P < 0.01).Serum concentrations of CXCL9 and CXCL10 in recipient mice were higher in the experimental group than those in the control group. Compared with the control group, the relative gene expressions of CXCL9 and CXCL10 were higher in the experimental group. According to pathological examinations, the histological rank of cardiac allograft was Grade 2.27 ± 0.25 in the control group versus Grade 4.12 ± 0.03 in the experimental group (P < 0.01).

CONCLUSIONS

CXCL9 and CXCL10 play critical roles in retransplantation mediated by alloreactive memory T cells. And acute rejection of cardiac allograft is more extensive in retransplantation.

摘要

目的

在再次移植模型中观察趋化因子CXCL9和CXCL10对同种异体反应性记忆T细胞介导的心脏移植急性排斥反应的影响。

方法

皮肤移植6周后进行心脏移植。将小鼠分为3组:对照组(直接异位心脏移植,未进行皮肤移植);实验组(皮肤移植后进行心脏移植)和同基因移植组(C57BL/6→C57BL/6,异位心脏移植)(每组n = 12)。观察移植物存活情况及心脏移植物的病理变化。检测心脏移植物中相关基因表达及血清CXCL9/CXCL10浓度。

结果

对照组和实验组的平均存活时间分别为7.75天和3.25天(P < 0.01)。实验组受体小鼠血清CXCL9和CXCL10浓度高于对照组。与对照组相比,实验组CXCL9和CXCL10的相对基因表达更高。病理检查显示,心脏同种异体移植物的组织学分级在对照组为2.27±0.25级,在实验组为4.12±0.03级(P < 0.01)。

结论

CXCL9和CXCL10在同种异体反应性记忆T细胞介导的再次移植中起关键作用。并且心脏同种异体移植物的急性排斥反应在再次移植中更广泛。

相似文献

1
[Roles of CXCL9 and CXCL10 in acute rejection after retransplantation in mice].[CXCL9和CXCL10在小鼠再次移植后急性排斥反应中的作用]
Zhonghua Yi Xue Za Zhi. 2014 May 27;94(20):1584-6.
2
CXCL9 and CXCL10 accelerate acute transplant rejection mediated by alloreactive memory T cells in a mouse retransplantation model.在小鼠再次移植模型中,CXCL9和CXCL10加速了由同种异体反应性记忆T细胞介导的急性移植排斥反应。
Exp Ther Med. 2014 Jul;8(1):237-242. doi: 10.3892/etm.2014.1714. Epub 2014 May 14.
3
Role of regulated upon activation normal T-cell expressed and secreted in a model of retransplantation acute rejection mediated by alloreactive memory CD4+ T cells.活化时正常T细胞表达和分泌产物在同种异体反应性记忆CD4+T细胞介导的再次移植急性排斥模型中的作用
Transplant Proc. 2013 Mar;45(2):546-51. doi: 10.1016/j.transproceed.2012.11.005.
4
Evaluation of CXCL9 and CXCL10 as circulating biomarkers of human cardiac allograft rejection.评估CXCL9和CXCL10作为人类心脏同种异体移植排斥反应循环生物标志物的情况。
BMC Cardiovasc Disord. 2006 Jun 19;6:29. doi: 10.1186/1471-2261-6-29.
5
CXC chemokine ligand (CXCL) 9 and CXCL10 are antagonistic costimulation molecules during the priming of alloreactive T cell effectors.CXC 趋化因子配体 (CXCL) 9 和 CXCL10 是在同种异体反应性 T 细胞效应器的激活过程中的拮抗共刺激分子。
J Immunol. 2010 Apr 1;184(7):3450-60. doi: 10.4049/jimmunol.0903831. Epub 2010 Mar 1.
6
Early up-regulation of CXC-chemokine expression is associated with strong cellular immune responses to murine skin xenografts.CXC趋化因子表达的早期上调与对小鼠皮肤异种移植的强烈细胞免疫反应相关。
Xenotransplantation. 2006 Jul;13(4):328-36. doi: 10.1111/j.1399-3089.2006.00311.x.
7
Intragraft expression of chemokine gene occurs early during acute rejection of allogeneic cardiac grafts.
Transplant Proc. 2000 Jun;32(4):793-5. doi: 10.1016/s0041-1345(00)00985-4.
8
I-TAC is a dominant chemokine in controlling skin intragraft inflammation via recruiting CXCR3+ cells into the graft.I-TAC 是一种优势趋化因子,通过招募 CXCR3+细胞进入移植物来控制皮肤移植物内炎症。
Cell Immunol. 2010;260(2):83-91. doi: 10.1016/j.cellimm.2009.09.004.
9
Combination of C-X-C motif chemokine 9 and C-X-C motif chemokine 10 antibodies with FTY720 prolongs the survival of cardiac retransplantation allografts in a mouse model.C-X-C基序趋化因子9和C-X-C基序趋化因子10抗体与FTY720联合使用可延长小鼠模型心脏再次移植同种异体移植物的存活时间。
Exp Ther Med. 2015 Mar;9(3):1006-1012. doi: 10.3892/etm.2015.2204. Epub 2015 Jan 22.
10
The recall alloresponse following retransplantation is more intense compared with the T cell memory-transfer model.与 T 细胞记忆转移模型相比,再移植后的召回同种异体反应更为强烈。
Immunol Invest. 2010;39(1):39-53. doi: 10.3109/08820130903410414.