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Enhanced Hematopoietic Stem Cell Self-Renewal-Promoting Ability of Clonal Primary Mesenchymal Stromal/Stem cells Versus Their Osteogenic Progeny

机译:增强的造血干细胞自我更新促进克隆初级间充质基质/干细胞与其成骨后代的促进能力

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Long-term self-renewing hematopoietic stem cell (LT-HSC) homeostasis within the bone marrow (BM) of adult mammals is regulated by complex interactions between LT-HSC and a number of niche-associated cell types including mesenchymal stromal/stem cells (MSC), osteoblasts (OB), macrophage, and neuronal cells in close proximity with the vasculature. Here, we cloned and functionally characterized a murine BM MSC subpopulation that was uniformly Nestin(+) Lepr (+)Sca-1(+)CD146(+) and could be stably propagated with high colony-forming unit fibroblast re-cloning efficiency. MSC synergized with SCF and IL-11 to support a 20-fold expansion in true LT-HSC after 10-days of in vitro coculture. Optimal stimulation of LT-HSC expansion was minimally dependent on Notch signaling but was significantly enhanced by global inhibition of Wnt signaling. The self-renewal-promoting activity of MSC was progressively lost when MSC clones were differentiated into mature OB. This suggests that the stage of osteoblast development may significantly impact the ability of osteolineage cells to support LT-HSC homeostasis in vivo.
机译:在成年哺乳动物的骨髓(BM)内的长期自我更新造血干细胞(LT-HSC)稳态受LT-HSC之间的复杂相互作用和包括间充质基质/干细胞( MSC),骨液细胞(OB),巨噬细胞和神经元细胞与脉管系统紧密接近。在此,我们克隆和功能性地表征了均匀巢(+)kePr(+)SCA-1(+)CD146(+)的鼠BM MSC亚泊素,并且可以稳定地与高菌落形成单位成纤维细胞重新克隆效率繁殖。 MSC通过SCF和IL-11协同作用,以在体外共培养10天后的True Lt-HSC中支持20倍的扩展。 LT-HSC膨胀的最佳刺激最小依赖于陷波信号传导,但通过全局抑制WNT信号传导显着提高。当MSC克隆分化为成熟OB时,MSC的自我重新启动促进活性逐渐丧失。这表明成骨细胞发育的阶段可能会显着影响骨液细胞在体内支持LT-HSC稳态的能力。

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