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Identification of the Human Skeletal Stem Cell

机译:鉴定人骨骼干细胞

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Stem cell regulation and hierarchical organization of human skeletal progenitors remain largely unexplored. Here, we report the isolation of a self-renewing and multipotent human skeletal stem cell (hSSC) that generates progenitors of bone, cartilage, and stroma, but not fat. Self-renewing and multipotent hSSCs are present in fetal and adult bones and can also be derived from BMP2-treated human adipose stroma (B-HAS) and induced pluripotent stem cells (iPSCs). Gene expression analysis of individual hSSCs reveals overall similarity between hSSCs obtained from different sources and partially explains skewed differentiation toward cartilage in fetal and iPSC-derived hSSCs. hSSCs undergo local expansion in response to acute skeletal injury. In addition, hSSC-derived stroma canmaintain human hematopoietic stem cells (hHSCs) in serum-free culture conditions. Finally, we combine gene expression and epigenetic data of mouse skeletal stem cells (mSSCs) and hSSCs to identify evolutionarily conserved and divergent pathways driving SSC-mediated skeletogenesis.
机译:人体骨骼祖细胞的干细胞调节和分层组织在很大程度上是未开发的。在这里,我们报告了自我更新和多能人骨骼干细胞(HSSC)的分离,产生骨骼,软骨和基质的祖细胞,但不脂肪。胎儿和成人骨骼中存在自我更新和多能HSSCs,也可以衍生自BMP2处理的人脂肪基质(B-具有)和诱导多能干细胞(IPSC)。单个HSSCs的基因表达分析揭示了从不同来源获得的HSSCs之间的总体相似性,并且部分解释胎儿和IPSC衍生的HSSC中的软骨偏差分化。 HSSCS响应急性骨骼损伤而接受局部扩张。此外,HSSC-衍生的基质可以培养物造血干细胞(HHSCs)在无血清培养条件下。最后,我们将小鼠骨干干细胞(MSSCs)和HSSCs的基因表达和表观遗传数据组合以识别驱动SSC介导的骨骼发生的进化和发散途径。

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