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首页> 外文期刊>Stem cells and development >Engraftment kinetics of human cord blood and murine fetal liver stem cells following in utero transplantation into immunodeficient mice.
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Engraftment kinetics of human cord blood and murine fetal liver stem cells following in utero transplantation into immunodeficient mice.

机译:子宫内移植到免疫缺陷小鼠体内后,人脐带血和鼠胎儿肝干细胞的植入动力学。

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This study was undertaken to evaluate the kinetics of engraftment after in utero transplantation of murine fetal liver and human cord blood stem cells in the nonobese diabetic/severe combined immunodeficient (NOD/SCID) mouse model. NOD/SCID fetuses were injected with murine fetal liver or human cord blood CD34+ cells at day 13.5 of gestation. Frequencies of donor cells were analyzed by flow cytometry up to 48 h post transplantation and 4-16 weeks postnatally. Hematopoietic multilineage reconstitution capacity was assessed. Both types of donor cells home rapidly. However, the frequency of human cord blood stem cells rapidly diminished while the murine fetal liver stem cells expanded over time, resulting in multilineage hematopoietic reconstitution. Differences in long-term reconstitution of allogeneic versus xenogeneic donor cells were ascribed to the inability of the human cells to self-renew and differentiate in the fetal mouse environment, demonstrating the limitations of this commonly used xenograph.
机译:进行这项研究以评估在非肥胖糖尿病/重度合并免疫缺陷(NOD / SCID)小鼠模型中子宫内移植鼠胎儿肝和人脐带血干细胞后的移植动力学。在妊娠第13.5天,向NOD / SCID胎儿注射鼠胎肝或人脐带血CD34 +细胞。通过流式细胞术分析供体细胞的频率,直至移植后48小时和出生后4-16周。评估了造血多系重建能力。两种类型的供体细胞都迅速归巢。然而,人类脐带血干细胞的频率迅速降低,而鼠胎儿肝干细胞随时间的流逝而膨胀,导致多谱系造血重建。异体供体细胞与异种供体细胞长期重建的差异归因于人类细胞无法在胎儿小鼠环境中自我更新和分化,这证明了这种常用异种检测仪的局限性。

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