首页> 外文期刊>Bone marrow transplantation >Stem cell factor improves SCID-repopulating activity of human umbilical cord blood-derived hematopoietic stem/progenitor cells in xenotransplanted NOD/SCID mouse model.
【24h】

Stem cell factor improves SCID-repopulating activity of human umbilical cord blood-derived hematopoietic stem/progenitor cells in xenotransplanted NOD/SCID mouse model.

机译:在异种移植的NOD / SCID小鼠模型中,干细胞因子可改善人脐带血来源的造血干/祖细胞的SCID再生活性。

获取原文
获取原文并翻译 | 示例
       

摘要

Poor in vivo homing capacity of hematopoietic stem/progenitor cells (HS/PCs) from umbilical cord blood (UCB) can be reversed by short-term ex vivo manipulation with recombinant human stem cell factor (rHuSCF). This study was designed to evaluate the effect of ex vivo manipulation of UCB-derived HS/PCs with rHuSCF on human cell engraftment rates in xenotransplanted NOD/SCID mouse model. The human cell engraftment rates in xenotransplanted primary and secondary NOD/SCID mice were characterized using four-color flow cytometric analysis and progenitor assay. Grafts of rHuSCF-treated UCB CD34(+) cells resulted in significantly higher levels of human cell engraftment than that of nontreated ones in both xenotransplanted primary and secondary NOD/SCID recipients. Fresh UCB CD34(+) cells did not express either of the matrix metalloproteinase (MMP) family members MMP-2 or MMP-9. rHuSCF-treated UCB CD34(+) cells expressed significant levels of MMP-2 and MMP-9. Pretreatment of UCB CD34(+) cells with the specific MMP inhibitor completely blocked human cell engraftment in xenotransplanted NOD/SCID recipients. Our results indicate that ex vivo manipulation of human HS/PCs with rHuSCF might provide an optimal approach to develop more effective stem cell-based therapies in situations where engraftment is delayed due to limiting HS/PCs number, for example, UCB transplantation.
机译:脐带血(UCB)造血干/祖细胞(HS / PCs)的体内归巢能力差,可以通过重组人干细胞因子(rHuSCF)的短期离体操作来逆转。这项研究旨在评估异种移植NOD / SCID小鼠模型中离体操作UCB衍生的HS / PCs和rHuSCF对人细胞植入率的影响。使用四色流式细胞仪分析和祖细胞测定来表征异种移植的原发和继发NOD / SCID小鼠的人类细胞植入率。在异种移植的主要和次要NOD / SCID受体中,rHuSCF处理的UCB CD34(+)细胞的移植导致人类细胞移植的水平明显高于未处理的人类细胞移植水平。新鲜的UCB CD34(+)细胞不表达基质金属蛋白酶(MMP)家族成员MMP-2或MMP-9。经rHuSCF处理的UCB CD34(+)细胞表达了显着水平的MMP-2和MMP-9。用特异的MMP抑制剂对UCB CD34(+)细胞进行预处理可以完全阻止异种移植NOD / SCID受体中人类细胞的植入。我们的结果表明,在由于限制HS / PC数量而导致移植延迟的情况下,例如UCB移植,使用rHuSCF对人HS / PC进行离体操作可能会提供一种开发更有效基于干细胞疗法的最佳方法。

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