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相互依赖的成纤维细胞生长因子和激活素A信号传导促进表达含Src同源2结构域失活型Shb的分化小鼠胚胎干细胞中内胚层基因的表达。

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.

作者信息

Funa Nina S, Saldeen Johan, Akerblom Björn, Welsh Michael

机构信息

Department of Medical Cell Biology, Uppsala University, Biomedical Centre, PO Box 571, Husargatan 3, SE-751 23, Uppsala, Sweden.

出版信息

Differentiation. 2008 May;76(5):443-53. doi: 10.1111/j.1432-0436.2007.00249.x. Epub 2007 Dec 17.

DOI:10.1111/j.1432-0436.2007.00249.x
PMID:18093225
Abstract

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 effects of 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.

摘要

尽管先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是一种含有Src同源2(SH2)结构域的衔接蛋白,已被证明与FGF受体1(FGFR1)信号传导有关。为了研究激活素A与Shb依赖的FGF信号在胚胎干细胞(ES细胞)向内胚层分化过程中的潜在相互作用,将过表达野生型Shb或带有突变SH2结构域的Shb(R522K-Shb)的小鼠ES细胞来源的胚状体(EBs)在激活素A存在的情况下进行培养。我们发现R522K-Shb的表达导致EBs中FGFR1和FGF2的上调。向培养物中添加激活素A主要增强了表达突变型Shb的EBs中内胚层基因的表达。添加FGFR1抑制剂SU5402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下游的某些信号通路,并且FGF和激活素A之间的相互作用参与了ES细胞向内胚层的分化。

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