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初级纤毛重构介导分化神经元中的细胞信号转换。

Primary cilium remodeling mediates a cell signaling switch in differentiating neurons.

机构信息

Division of Molecular and Cellular Function, Faculty of Biology Medicine and Health, University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.

出版信息

Sci Adv. 2020 May 20;6(21):eabb0601. doi: 10.1126/sciadv.abb0601. eCollection 2020 May.

Abstract

Cellular differentiation leads to the formation of specialized cell types and complex morphological variations. Often, differentiating cells transition between states by switching how they respond to the signaling environment. However, the mechanisms regulating these transitions are poorly understood. Differentiating neurons delaminate from the neuroepithelium through the regulated process of apical abscission, which mediates an acute loss of polarity and primary cilium disassembly. Using high-resolution live-cell imaging in chick neural tube, we show that these cells retain an Arl13b particle, which elongates and initiates intraflagellar trafficking as it transits toward the cell body, indicating primary cilium remodeling. Notably, disrupting cilia during and after remodeling inhibits axon extension and leads to axon collapse, respectively. Furthermore, cilium remodeling corresponds to a switch from a canonical to noncanonical cellular response to Shh. This work transforms our understanding of how cells can rapidly reinterpret signals to produce qualitatively different responses within the same tissue context.

摘要

细胞分化导致特化细胞类型和复杂形态变化的形成。通常,分化细胞通过改变对信号环境的反应方式在状态之间转换。然而,调节这些转变的机制知之甚少。分化神经元通过调节的顶端分离过程从神经上皮层分离,这介导了极性的急剧丧失和初级纤毛的解体。使用鸡神经管中的高分辨率活细胞成像,我们表明这些细胞保留了 Arl13b 颗粒,该颗粒在向细胞体迁移时伸长并启动鞭毛内运输,表明初级纤毛重塑。值得注意的是,在重塑过程中和重塑后破坏纤毛分别抑制轴突延伸和导致轴突塌陷。此外,纤毛重塑与从 Shh 的经典到非经典细胞反应的转变相对应。这项工作改变了我们对细胞如何能够快速重新解释信号以在相同组织背景下产生定性不同的反应的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3164/7252506/c560f7ed3249/abb0601-F1.jpg

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