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Efficient induction of osteogenic and chondrogenic progenitors and myogenic progenitors from mouse ES cells in chemically defined medium

机译:从化学定义培养基中的小鼠ES细胞中高效诱导骨质发生和软骨祖细胞和肌原血管原血管发射菌

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Embryonic stem (ES) cells and induced pluripotent stem (iPS) cells represent a renewable cellular resources for regenerative therapies. Here, we try to differentiate ES cells to paraxial mesodermal progenitors cells (PMPs), which give rise to osteogenic and chondrogenic progenitors and myogenic progenitors without fetal calf serum. Here, we demonstrate the methods for inducing paraxial mesodermal progenitors efficiently by treatment of BMP4 using PDGFR-a and ECD as markers for purifying them. The BMP4 induced PMPs exhibit fine potentials of differentiation to osto-and chondro-genic cells. Furthermore, early extraction of BMP4 and additional LiCl treatment promote the differentiation of myogenic progenitor cells. Further addition of IGF-1, bFGF and HGF induced the differentiation of PMPs to myocytes in vitro.
机译:胚胎茎(ES)细胞和诱导多能干(IPS)细胞代表可再生疗法的可再生细胞资源。在此,我们尝试将ES细胞分化为瘫痪的中胚层祖细胞(PMP),其导致骨质发生和软骨内祖细胞和肌原血管血清的肌原血清。在这里,我们通过使用PDGFR-A和ECD作为标记用PDGFR-A和ECD治疗BMP4作为用于净化它们的标记,证明了用于诱导瘫痪性中胚层祖细胞的方法。 BMP4诱导的PMP表现出与osto-and软骨基因细胞分化的细势。此外,早期提取BMP4和另外的LICL治疗促进了肌原源性祖细胞的分化。进一步添加IGF-1,BFGF和HGF在体外诱导PMP与肌细胞的分化。

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