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Molecularly and temporally separable lineages form the hindbrain roof plate and contribute differentially to the choroid plexus.

机译:分子和时间上可分离的谱系形成后脑顶板,并在脉络丛中起不同作用。

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Both hindbrain roof plate epithelium (hRPe) and hindbrain choroid plexus epithelium (hCPe) produce morphogens and growth factors essential for proper hindbrain development. Despite their importance, little is known about how these essential structures develop. Recent genetic fate maps indicate that hRPe and hCPe descend from the same pool of dorsal neuroectodermal progenitor cells of the rhombic lip. A linear developmental progression has been assumed, with the rhombic lip producing non-mitotic hRPe, and seemingly uniform hRPe transforming into hCPe. Here, we show that hRPe is not uniform but rather comprises three spatiotemporal fields, which differ in organization, proliferative state, order of emergence from the rhombic lip, and molecular profile of either the constituent hRPe cells themselves and/or their parental progenitors. Only two fields contribute to hCPe. We also present evidence for an hCPe contribution directly by the rhombic lip at late embryonic stages when hRPe is no longer present; indeed, the production interval for hCPe by the rhombic lip is surprisingly extensive. Further, we show that the hCPe lineage appears to be unique among the varied rhombic lip-derived lineages in its proliferative response to constitutively active Notch1 signaling. Collectively, these findings provide a new platform for investigating hRPe and hCPe as neural organizing centers and provide support for the model that they are themselves patterned structures that might be capable of influencing neural development along multiple spatial and temporal axes.
机译:后脑顶板上皮(hRPe)和后脑脉络丛神经上皮(hCPe)均会产生形成适当的后脑所需的形态发生因子和生长因子。尽管它们很重要,但对于这些基本结构的发展方式知之甚少。最近的遗传命运图谱表明,hRPe和hCPe来自菱形唇的背神经外胚层祖细胞的同一集合。假定线性发展进程,菱形唇产生非有丝分裂的hRPe,看似均匀的hRPe转变为hCPe。在这里,我们显示出hRPe不是统一的,而是包括三个时空场,它们在组织,增殖状态,菱形唇的出现顺序以及组成的hRPe细胞本身和/或其亲代祖先的分子分布方面有所不同。只有两个字段对hCPe有所贡献。我们还提供了证据,表明在hRPe不再存在时,菱形唇在胚胎晚期就直接贡献了hCPe。实际上,菱形唇产生hCPe的间隔令人惊讶地广泛。此外,我们表明,hCPe谱系在其对组成型活性Notch1信号的增殖反应中似乎在各种菱形唇来源的谱系中是独特的。总的来说,这些发现为研究hRPe和hCPe作为神经组织中心提供了一个新平台,并为该模型本身是模式化的结构提供了支持,这些结构可能会影响多个时空轴上的神经发育。

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