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Dynamic roles of angiopoietin-like proteins 1, 2, 3, 4, 6 and 7 in the survival and enhancement of ex vivo expansion of bone-marrow hematopoietic stem cells

机译:血管生成素样蛋白1、2、3、4、6和7在骨髓造血干细胞的体外存活和增强中的动态作用

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Recent advances in hematopoietic stem cells (HSCs) expansion by growth factors including angiopoietin-like proteins (Angptls) have opened up the possibility to use HSCs in regenerative medicine. However, the unavailability of true in vitro HSCs expansion by these growth factors has limited the understanding of the cellular and molecular mechanism of HSCs expansion. Here, we report the functional role of mouse Angptls 1, 2, 3, 4, 6 and 7 and growth factors SCF, TPO, IGF-2 and FGF-1 on purified mouse bone-marrow (BM) Lineage?Sca-1+(Lin-Sca-1+) HSCs. The recombinant retroviral transduced-CHO-S cells that secrete Angptls in serum-free medium were used alone or in combination with growth factors (SCF, TPO, IGF-2 and FGF-1). None of the Angptls stimulated HSC proliferation, enhanced or inhibited HSCs colony formation, but they did support the survival of HSCs. By contrast, any of the six Angptls together with saturating levels of growth factors dramatically stimulated a 3- to 4.5-fold net expansion of HSCs compared to stimulation with a combination of those growth factors alone. These findings lead to an understanding of the basic function of Angptls on signaling pathways for the survival as well as expansion of HSCs in the bone marrow niche.
机译:包括血管生成素样蛋白(Angptls)在内的生长因子在造血干细胞(HSC)扩增方面的最新进展为在再生医学中使用HSC提供了可能性。但是,这些生长因子无法提供真正的体外HSC扩增,限制了对HSC扩增的细胞和分子机制的了解。在这里,我们报告小鼠角蛋白1、2、3、4、6和7以及生长因子SCF,TPO,IGF-2和FGF-1对纯化的小鼠骨髓(BM)谱系的功能作用 Sca-1 + (Lin-Sca-1 + )HSC。在无血清培养基中分泌Angptl的重组逆转录病毒转导的CHO-S细胞可以单独使用,也可以与生长因子(SCF,TPO,IGF-2和FGF-1)结合使用。 Angptls均不刺激HSC增殖,增强或抑制HSC菌落形成,但它们确实支持HSC的存活。相比之下,与单独使用这些生长因子的刺激相比,六个Angptl中的任何一个都与饱和水平的生长因子一起显着刺激了HSC的3到4.5倍的净膨胀。这些发现导致对Angptls在骨髓小生境中HSC的存活和扩增的信号传导途径的基本功能的理解。

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