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首页> 外文期刊>Mechanisms of Development >Unexpected activities of Smad7 in Xenopus mesodermal and neural induction.
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Unexpected activities of Smad7 in Xenopus mesodermal and neural induction.

机译:Smad7在非洲爪蟾中胚层和神经诱导中的意外活动。

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摘要

Neural induction is widely believed to be a direct consequence of inhibition of BMP pathways. Because of conflicting results and interpretations, we have re-examined this issue in Xenopus and chick embryos using the powerful and general TGFbeta inhibitor, Smad7, which inhibits both Smad1- (BMP) and Smad2- (Nodal/Activin) mediated pathways. We confirm that Smad7 efficiently inhibits phosphorylation of Smad1 and Smad2. Surprisingly, however, over-expression of Smad7 in Xenopus ventral epidermis induces expression of the dorsal mesodermal markers Chordin and Brachyury. Neural markers are induced, but in a non-cell-autonomous manner and only when Chordin and Brachyury are also induced. Simultaneous inhibition of Smad1 and Smad2 by different approaches does not account for all Smad7 effects, indicating that Smad7 has activities other than inhibition of the TGFbeta pathway. We provide evidence that these effects are independent of Wnt, FGF, Hedgehog and retinoid signalling. We also show that these effects are due to elements outside of the MH2 domain of Smad7. Together, these results indicate that BMP inhibition is not sufficient for neural induction even when Nodal/Activin is also blocked, and that Smad7 activity is considerably more complex than had previously been assumed. We suggest that experiments relying on Smad7 as an inhibitor of TGFbeta-pathways should be interpreted with considerable caution.
机译:广泛认为神经诱导是抑制BMP途径的直接结果。由于存在矛盾的结果和解释,我们使用功能强大且通用的TGFbeta抑制剂Smad7在Xenopus和雏鸡胚胎中重新检查了此问题,该抑制剂可抑制Smad1-(BMP)和Smad2-(Nodal / Activin)介导的途径。我们证实Smad7有效抑制Smad1和Smad2的磷酸化。然而,令人惊讶的是,非洲爪蟾腹侧表皮中Smad7的过表达诱导了背中胚层标记Chordin和Brachyury的表达。诱导神经标记,但是以非细胞自主方式,并且仅在也诱导Chordin和Brachyury时才诱导。通过不同方法同时抑制Smad1和Smad2并不能说明所有Smad7效应,这表明Smad7除抑制TGFbeta途径外还具有其他活性。我们提供的证据表明,这些作用与Wnt,FGF,刺猬和类维生素A信号无关。我们还表明,这些影响是由于Smad7的MH2域之外的元素引起的。总之,这些结果表明,即使当Nodal / Activin也被阻滞时,BMP抑制仍不足以诱导神经,并且Smad7活性比以前假定的要复杂得多。我们建议依赖Smad7作为TGFbeta途径抑制剂的实验应谨慎对待。

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