Shimoda Marine Research Center, University of Tsukuba, Japan.
Dev Biol. 2010 Nov 1;347(1):71-81. doi: 10.1016/j.ydbio.2010.08.009. Epub 2010 Aug 12.
The ciliary band is a distinct region of embryonic ectoderm that is specified between oral and aboral ectoderm. Flask-shaped ciliary cells and neurons differentiate in this region and they are patterned to form an integrated tissue that functions as the principal swimming and feeding organ of the larva. TGFβ signaling, which is known to mediate oral and aboral patterning of the ectoderm, has been implicated in ciliary band formation. We have used morpholino knockdown and ectopic expression of RNA to alter TGFβ signaling at the level of ligands, receptors, and signal transduction components and assessed the differentiation and patterning of the ciliary band cells and associated neurons. We propose that the primary effects of these signals are to position the ciliary cells, which in turn support neural differentiation. We show that Nodal signaling, which is known to be localized by Lefty, positions the oral margin of the ciliary band. Signaling from BMP through Alk3/6, affects the position of the oral and aboral margins of the ciliary band. Since both Nodal and BMP signaling produce ectoderm that does not support neurogenesis, we propose that formation of a ciliary band requires protection from these signals. Expression of BMP2/4 and Nodal suppress neural differentiation. However, the response to receptor knockdown or dominant-negative forms of signal transduction components indicate signaling is not acting directly on unspecified ectoderm cells to prevent their differentiation as neurons. Instead, it produces a restricted field of ciliary band cells that supports neurogenesis. We propose a model that incorporates spatially regulated control of Nodal and BMP signaling to determine the position and differentiation of the ciliary band, and subsequent neural patterning.
纤毛带是胚胎外胚层的一个独特区域,在口侧和肛侧外胚层之间被特化。在此区域分化出瓶状纤毛细胞和神经元,并对其进行组织模式化,形成一个整合的组织,作为幼虫的主要游泳和进食器官。已知 TGFβ 信号转导介导外胚层的口侧和肛侧模式形成,它与纤毛带的形成有关。我们使用形态发生素敲低和 RNA 异位表达来改变配体、受体和信号转导成分的 TGFβ 信号转导,并评估纤毛带细胞和相关神经元的分化和模式形成。我们提出,这些信号的主要作用是定位纤毛细胞,纤毛细胞反过来又支持神经分化。我们表明,Lefty 定位的 Nodal 信号定位纤毛带的口侧边缘。BMP 通过 Alk3/6 发出的信号影响纤毛带的口侧和肛侧边缘的位置。由于 Nodal 和 BMP 信号都产生不支持神经发生的外胚层,我们提出形成纤毛带需要免受这些信号的保护。BMP2/4 和 Nodal 的表达抑制神经分化。然而,对受体敲低或信号转导成分的显性负形式的反应表明,信号不是直接作用于未指定的外胚层细胞,以防止其分化为神经元。相反,它产生了一个受限制的纤毛带细胞区,支持神经发生。我们提出了一个模型,该模型将 Nodal 和 BMP 信号的空间调节控制纳入其中,以确定纤毛带的位置和分化,以及随后的神经模式形成。