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胚外干细胞通过嵌合体胚胎形成显示出体内分化潜能。

In Vivo differentiation potential of epiblast stem cells revealed by chimeric embryo formation.

机构信息

MRC Centre for Regenerative Medicine, School of Biological Sciences, University of Edinburgh, Edinburgh bioQuarter, Edinburgh, UK.

出版信息

Cell Rep. 2012 Dec 27;2(6):1571-8. doi: 10.1016/j.celrep.2012.10.022. Epub 2012 Nov 29.

Abstract

Chimera formation after blastocyst injection or morula aggregation is the principal functional assay of the developmental potential of mouse embryonic stem cells (ESCs). This property, which demonstrates functional equivalence between ESCs and the preimplantation epiblast, is not shared by epiblast stem cell (EpiSC) lines. Here, we show that EpiSCs derived either from postimplantation embryos or from ESCs in vitro readily generate chimeras when grafted to postimplantation embryos in whole embryo culture. EpiSC derivatives integrate and differentiate to derivatives of all three embryonic germ layers and primordial germ cells. In contrast, grafted ESCs seldom proliferate in postimplantation embryos, and fail to acquire the identity of their host-derived neighbors. EpiSCs do not incorporate efficiently into embryonic day 8.5 embryos, a stage by which pluripotency has been lost. Thus, chimera formation by EpiSCs requires a permissive environment, the postimplantation epiblast, and demonstrates functional equivalence between this cell type and EpiSCs.

摘要

囊胚注射或桑葚胚聚集后形成嵌合体是检测小鼠胚胎干细胞(ESC)发育潜能的主要功能检测方法。这种特性表明 ESC 和着床前的上胚层具有功能等同性,但上胚层干细胞(EpiSC)系并不具备这种特性。在这里,我们发现无论是源自着床后胚胎还是源自体外 ESC 的 EpiSC,在整个胚胎培养中移植到着床后胚胎时,都很容易生成嵌合体。EpiSC 衍生物可整合并分化为所有三个胚胎生殖层和原始生殖细胞的衍生物。相比之下,移植的 ESC 很少在着床后胚胎中增殖,并且无法获得其宿主来源的邻近细胞的特性。EpiSC 不能有效地掺入到胚胎发育第 8.5 天的胚胎中,因为此时多能性已经丧失。因此,EpiSC 形成嵌合体需要一个允许的环境,即着床后的上胚层,并证明这种细胞类型与 EpiSC 之间具有功能等同性。

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