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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Membrane-bound human SCF/KL promotes in vivo human hematopoietic engraftment and myeloid differentiation
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Membrane-bound human SCF/KL promotes in vivo human hematopoietic engraftment and myeloid differentiation

机译:膜结合人类SCF / KL促进体内人类造血移植和骨髓分化

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In recent years, advances in the humanized mouse system have led to significantly increased levels of human hematopoietic stem cell (HSC) engraftment. The remaining limitations in human HSC engraftment and function include lymphoidskewed differentiation and inefficient myeloid development in the recipients. Limited human HSC function may partially be attributed to the inability of the host mouse microenvironment to provide sufficient support to human hematopoiesis. To address this problem, we created membrane-bound human stem cell factor (SCF)/KIT ligand (KL)-expressing NOD/SCID/IL2rgKO (hSCF Tg NSG) mice. hSCF Tg NSG recipients of human HSCs showed higher levels of both human CD45 + cell engraftment and human CD45 +CD33 + myeloid development compared with NSG recipients. Expression of hSCF/hKL accelerated the differentiation of the human granulocyte lineage cells in the recipient bone marrow. Human mast cells were identified in bone marrow, spleen, and gastrointestinal tissues of the hSCF Tg NSG recipients. This novel in vivo humanized mouse model demonstrates the essential role of membranebound hSCF in human myeloid development. Moreover, the hSCF Tg NSG humanized recipients may facilitate investigation of in vivo differentiation, migration, function, and pathology of human mast cells.
机译:近年来,人性化小鼠系统的进步已导致人类造血干细胞(HSC)植入水平显着提高。人类HSC植入和功能的其余局限性包括受体的淋巴样偏斜分化和无效的骨髓发育。人类HSC功能有限可能部分归因于宿主小鼠微环境无法为人类造血提供足够的支持。为了解决此问题,我们创建了表达膜结合人干细胞因子(SCF)/ KIT配体(KL)的NOD / SCID / IL2rgKO(hSCF Tg NSG)小鼠。与NSG接受者相比,人类HSC的hSCF Tg NSG接受者显示出更高水平的人类CD45 +细胞植入和人类CD45 + CD33 +骨髓发育。 hSCF / hKL的表达加速了受体骨髓中人类粒细胞谱系细胞的分化。在hSCF Tg NSG受体的骨髓,脾脏和胃肠道组织中鉴定出人类肥大细胞。这种新颖的体内人源化小鼠模型证明了膜结合的hSCF在人类骨髓发育中的重要作用。此外,hSCF Tg NSG人源化受体可能有助于研究人类肥大细胞的体内分化,迁移,功能和病理。

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