...
首页> 外文期刊>Journal of cellular and molecular medicine. >Role of HLA-G and NCR in protection of umbilical cord blood haematopoietic stem cells from NK cell mediated cytotoxicity
【24h】

Role of HLA-G and NCR in protection of umbilical cord blood haematopoietic stem cells from NK cell mediated cytotoxicity

机译:HLA-G和NCR在保护脐血造血干细胞免受NK细胞介导的细胞毒性作用中的作用

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Allogeneic umbilical cord blood haematopoietic stem cells (UCB–HSCs) can be transplanted into a host with the intact innate immunity with limited immuno-reaction, although the mechanisms remain unclear. The present studies aimed at investigating potential mechanisms of allogeneic UCB–HSCs escape from the cytolysis of natural killer (NK) cells. We compared UCB–HSCs ability to protect from NK-mediated cytotoxicity with peripheral blood or bone marrow haematopoietic stem cells (PB-HSCs and BM-HSCs). HSCs expressed lower levels of natural cytotoxicity receptor ligands including NKp30L, NKp44L and NKp46L than monocytes. Blocking these ligands respectively or in combination could increase the resistance of HSCs against NK cell mediated cytotoxicity. High expression of HLA-G was noticed on UCB–HSCs, rather than PB-HSCs or BM-HSCs, whereas blockade of HLA-G significantly elevated NK cell mediated cytolysis to UCB–HSCs. Thus, we conclude that natural cytotoxicity receptors and HLA-G on HSCs may contribute to the escape from NK cells, and activate and inhibitory NK cell receptors and their ligands can be novel therapeutic targets in cell transplantation.
机译:异基因脐带血造血干细胞(UCB–HSCs)可以被移植到具有完整先天免疫力且免疫反应有限的宿主中,尽管其机制尚不清楚。目前的研究旨在调查同种异体UCB–HSC逃脱天然杀伤(NK)细胞的潜在机制。我们比较了UCB–HSC与外周血或骨髓造血干细胞(PB-HSC和BM-HSC)防止NK介导的细胞毒性的能力。 HSCs表达的天然细胞毒性受体配体(包括NKp30L,NKp44L和NKp46L)的水平低于单核细胞。分别或组合阻断这些配体可增加HSC对NK细胞介导的细胞毒性的抗性。在UCB–HSC而不是PB-HSC或BM-HSC上注意到了HLA-G的高表达,而对HLA-G的阻断显着提高了NK细胞介导的对UCB–HSC的细胞溶解。因此,我们得出结论,HSC上的天然细胞毒性受体和HLA-G可能有助于从NK细胞逃逸,活化和抑制性NK细胞受体及其配体可以成为细胞移植中的新型治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号