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首页> 外文期刊>Differentiation: The Journal of the International Society of Differentiation >Interdependent fibroblast growth factor and activin A signaling promotes the expression of endodermal genes in differentiating mouse embryonic stem cells expressing Src Homology 2-domain inactive Shb.
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Interdependent fibroblast growth factor and activin A signaling promotes the expression of endodermal genes in differentiating mouse embryonic stem cells expressing Src Homology 2-domain inactive Shb.

机译:相互依赖的成纤维细胞生长因子和激活素A信号传导促进内胚基因在分化小鼠胚胎干细胞中表达Src同源2域失活Shb的表达。

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摘要

The mechanisms controlling endodermal development during stem cell differentiation have been only partly elucidated, although previous studies have suggested the participation of fibroblast growth factor (FGF) and activin A in these processes. Shb is a Src homology 2 (SH2) domain-containing adapter protein that has been implicated in FGF receptor 1 (FGFR1) signaling. To study the putative crosstalk between activin A and Shb-dependent FGF signaling in the differentiation of endoderm from embryonic stem (ES) cells, embryoid bodies (EBs) derived from mouse ES cells overexpressing wild-type Shb or Shb with a mutated SH2 domain (R522K-Shb) were cultured in the presence of activin A. We show that expression of R522K-Shb results in up-regulation of FGFR1 and FGF2 in EBs. Addition of activin A to the cultures enhances the expression of endodermal genes primarily in EBs expressing mutant Shb. Inhibition of FGF signaling by the addition of the FGFR1 inhibitor SU5402 completely counteracts the synergistic effectsof R522K-Shb and activin A. In conclusion, the present results suggest that expression of R522K-Shb enhances certain signaling pathways downstream of FGF and that an interplay between FGF and activin A participates in ES cell differentiation to endoderm.
机译:尽管以前的研究表明成纤维细胞生长因子(FGF)和激活素A参与了这些过程,但在干细胞分化过程中控制内胚层发育的机制仅得到了部分阐明。 Shb是一种包含Src同源2(SH2)域的衔接蛋白,已与FGF受体1(FGFR1)信号传导有关。为了研究激活素A和Shb依赖性FGF信号通路在胚胎干(ES)细胞的内胚层分化中的假定串扰,源自小鼠ES细胞的类胚体(EB)过量表达野生型Shb或具有突变的SH2结构域的Shb( R522K-Shb)在激活素A的存在下培养。我们显示R522K-Shb的表达导致EB中FGFR1和FGF2的上调。向培养物中添加激活素A主要在表达突变型Shb的EB中增强内胚层基因的表达。通过添加FGFR1抑制剂SU5402来抑制FGF信号传导完全抵消了R522K-Shb和激活素A的协同作用。总之,目前的结果表明,R522K-Shb的表达增强了FGF下游的某些信号传导途径,并且FGF之间的相互作用激活素A参与ES细胞向内胚层的分化。

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