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钙黏蛋白在早期神经发育中的作用。

Cadherins in early neural development.

机构信息

Helsinki Institute of Life Science, Biomedicum Helsinki, University of Helsinki, 00290, Helsinki, Finland.

Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290, Helsinki, Finland.

出版信息

Cell Mol Life Sci. 2021 May;78(9):4435-4450. doi: 10.1007/s00018-021-03815-9. Epub 2021 Apr 1.

Abstract

During early neural development, changes in signalling inform the expression of transcription factors that in turn instruct changes in cell identity. At the same time, switches in adhesion molecule expression result in cellular rearrangements that define the morphology of the emerging neural tube. It is becoming increasingly clear that these two processes influence each other; adhesion molecules do not simply operate downstream of or in parallel with changes in cell identity but rather actively feed into cell fate decisions. Why are differentiation and adhesion so tightly linked? It is now over 60 years since Conrad Waddington noted the remarkable "Constancy of the Wild Type" (Waddington in Nature 183: 1654-1655, 1959) yet we still do not fully understand the mechanisms that make development so reproducible. Conversely, we do not understand why directed differentiation of cells in a dish is sometimes unpredictable and difficult to control. It has long been suggested that cells make decisions as 'local cooperatives' rather than as individuals (Gurdon in Nature 336: 772-774, 1988; Lander in Cell 144: 955-969, 2011). Given that the cadherin family of adhesion molecules can simultaneously influence morphogenesis and signalling, it is tempting to speculate that they may help coordinate cell fate decisions between neighbouring cells in the embryo to ensure fidelity of patterning, and that the uncoupling of these processes in a culture dish might underlie some of the problems with controlling cell fate decisions ex-vivo. Here we review the expression and function of cadherins during early neural development and discuss how and why they might modulate signalling and differentiation as neural tissues are formed.

摘要

在早期神经发育过程中,信号的变化会告知转录因子的表达,而转录因子又会指示细胞身份的变化。与此同时,黏附分子表达的转换会导致细胞重排,从而定义新兴神经管的形态。越来越明显的是,这两个过程相互影响;黏附分子并不是简单地在细胞身份变化的下游或平行运行,而是积极地影响细胞命运的决定。为什么分化和黏附如此紧密地联系在一起?自从 Conrad Waddington 指出惊人的“野生型的恒定性”(Waddington 在 Nature 183: 1654-1655, 1959)以来已经过去了 60 多年,但我们仍然不完全理解使发育如此具有可重复性的机制。相反,我们也不理解为什么在培养皿中定向分化细胞有时是不可预测的和难以控制的。长期以来,人们一直认为细胞作为“局部合作体”而不是个体做出决定(Gurdon 在 Nature 336: 772-774, 1988;Lander 在 Cell 144: 955-969, 2011)。鉴于黏附分子家族的钙黏蛋白可以同时影响形态发生和信号转导,人们不禁推测它们可能有助于协调胚胎中相邻细胞的命运决定,以确保模式形成的保真度,并且在培养皿中这些过程的解耦可能是体外控制细胞命运决定的一些问题的基础。在这里,我们回顾了钙黏蛋白在早期神经发育过程中的表达和功能,并讨论了它们如何以及为什么可能调节信号转导和分化,因为神经组织正在形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f32f/11071931/d3603b89a241/18_2021_3815_Fig1_HTML.jpg

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