Ellis Pamela S, Burbridge Sarah, Soubes Sandrine, Ohyama Kyoji, Ben-Haim Nadav, Chen Canhe, Dale Kim, Shen Michael M, Constam Daniel, Placzek Marysia
The Bateson Centre and Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
ISREC, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Epalinges CH 1066, Switzerland.
Development. 2015 Nov 15;142(22):3821-32. doi: 10.1242/dev.119628. Epub 2015 Sep 28.
The secreted glycoprotein sonic hedgehog (Shh) is expressed in the prechordal mesoderm, where it plays a crucial role in induction and patterning of the ventral forebrain. Currently little is known about how Shh is regulated in prechordal tissue. Here we show that in the embryonic chick, Shh is expressed transiently in prechordal mesoderm, and is governed by unprocessed Nodal. Exposure of prechordal mesoderm microcultures to Nodal-conditioned medium, the Nodal inhibitor CerS, or to an ALK4/5/7 inhibitor reveals that Nodal is required to maintain both Shh and Gsc expression, but whereas Gsc is largely maintained through canonical signalling, Nodal signals through a non-canonical route to maintain Shh. Further, Shh expression can be maintained by a recombinant Nodal cleavage mutant, proNodal, but not by purified mature Nodal. A number of lines of evidence suggest that proNodal acts via FGFR3. ProNodal and FGFR3 co-immunoprecipitate and proNodal increases FGFR3 tyrosine phosphorylation. In microcultures, soluble FGFR3 abolishes Shh without affecting Gsc expression. Further, prechordal mesoderm cells in which Fgfr3 expression is reduced by Fgfr3 siRNA fail to bind to proNodal. Finally, targeted electroporation of Fgfr3 siRNA to prechordal mesoderm in vivo results in premature Shh downregulation without affecting Gsc. We report an inverse correlation between proNodal-FGFR3 signalling and pSmad1/5/8, and show that proNodal-FGFR3 signalling antagonises BMP-mediated pSmad1/5/8 signalling, which is poised to downregulate Shh. Our studies suggest that proNodal/FGFR3 signalling governs Shh duration by repressing canonical BMP signalling, and that local BMPs rapidly silence Shh once endogenous Nodal-FGFR3 signalling is downregulated.
分泌型糖蛋白音猬因子(Shh)在前索中胚层表达,在腹侧前脑的诱导和模式形成中起关键作用。目前对于Shh在前索组织中的调控方式知之甚少。在此我们表明,在胚胎鸡中,Shh在前索中胚层短暂表达,并受未加工的Nodal调控。将前索中胚层微培养物暴露于Nodal条件培养基、Nodal抑制剂CerS或ALK4/5/7抑制剂,结果表明Nodal对于维持Shh和Gsc的表达均是必需的,但是Gsc主要通过经典信号通路得以维持,而Nodal通过非经典途径发出信号以维持Shh。此外,重组的Nodal裂解突变体proNodal可维持Shh的表达,但纯化的成熟Nodal则不能。大量证据表明proNodal通过FGFR3发挥作用。ProNodal和FGFR3可进行共免疫沉淀,且proNodal可增加FGFR3酪氨酸磷酸化。在微培养物中,可溶性FGFR3可消除Shh的表达而不影响Gsc的表达。此外,通过Fgfr3 siRNA降低Fgfr3表达的前索中胚层细胞无法与proNodal结合。最后,在体内将Fgfr3 siRNA靶向电穿孔至前索中胚层会导致Shh过早下调而不影响Gsc。我们报告了proNodal - FGFR3信号与pSmad1/5/8之间呈负相关,并表明proNodal - FGFR3信号拮抗BMP介导的pSmad1/5/8信号,而BMP介导的信号准备下调Shh。我们的研究表明,proNodal/FGFR3信号通过抑制经典BMP信号来控制Shh的持续时间,并且一旦内源性Nodal - FGFR3信号下调,局部BMP会迅速使Shh沉默。