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使用胚胎干细胞诱导原始条纹形成的体外模型需要Wnt和TGF-β信号传导。

Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells.

作者信息

Gadue Paul, Huber Tara L, Paddison Patrick J, Keller Gordon M

机构信息

Department of Gene and Cell Medicine, Black Family Stem Cell Institute, Mount Sinai School of Medicine, 1 Gustave Levy Place, Box 1496, New York, NY 10029, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16806-11. doi: 10.1073/pnas.0603916103. Epub 2006 Oct 31.

Abstract

The establishment of the primitive streak and its derivative germ layers, mesoderm and endoderm, are prerequisite steps in the formation of many tissues. To model these developmental stages in vitro, an ES cell line was established that expresses CD4 from the foxa2 locus in addition to GFP from the brachyury locus. A GFP-Bry(+) population expressing variable levels of CD4-Foxa2 developed upon differentiation of this ES cell line. Analysis of gene-expression patterns and developmental potential revealed that the CD4-Foxa2(hi)GFP-Bry(+) population displays characteristics of the anterior primitive streak, whereas the CD4-Foxa2(lo)GFP-Bry(+) cells resemble the posterior streak. Using this model, we were able to demonstrate that Wnt and TGF-beta/nodal/activin signaling simultaneously were required for the generation of the CD4-Foxa2(+)GFP-Bry(+) population. Wnt or low levels of activin-induced a posterior primitive streak population, whereas high levels of activin resulted in an anterior streak fate. Finally, sustained activin signaling was found to stimulate endoderm commitment from the CD4-Foxa2(+)GFP-Bry(+) ES cell population. These findings demonstrate that the early developmental events involved in germ-layer induction in the embryo are recapitulated in the ES cell model and uncover insights into the signaling pathways involved in the establishment of mesoderm and endoderm.

摘要

原条及其衍生的胚层(中胚层和内胚层)的形成是许多组织形成的前提步骤。为了在体外模拟这些发育阶段,建立了一种胚胎干细胞系,该细胞系除了从短尾基因座表达绿色荧光蛋白(GFP)外,还从叉头框A2基因座表达CD4。该胚胎干细胞系分化后形成了表达水平各异的CD4-Foxa2的GFP-Bry(+)细胞群体。对基因表达模式和发育潜能的分析表明,CD4-Foxa2(hi)GFP-Bry(+)细胞群体表现出前原条的特征,而CD4-Foxa2(lo)GFP-Bry(+)细胞类似于后原条。利用该模型,我们能够证明Wnt信号通路和TGF-β/节点蛋白/激活素信号通路同时参与了CD4-Foxa2(+)GFP-Bry(+)细胞群体的产生。Wnt信号或低水平的激活素诱导产生后原条细胞群体,而高水平的激活素则导致前原条命运。最后,发现持续的激活素信号可刺激CD4-Foxa2(+)GFP-Bry(+)胚胎干细胞群体向内胚层定向分化。这些发现表明,胚胎中胚层和内胚层诱导过程中涉及的早期发育事件在胚胎干细胞模型中得以重现,并揭示了参与中胚层和内胚层形成的信号通路。

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