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Cold Spring Harb Perspect Biol. 2017 May 1;9(5):a028175. doi: 10.1101/cshperspect.a028175.
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Microtubule Motors Drive Hedgehog Signaling in Primary Cilia.微管马达蛋白驱动初级纤毛中的刺猬信号通路。
Trends Cell Biol. 2017 Feb;27(2):110-125. doi: 10.1016/j.tcb.2016.09.010. Epub 2016 Oct 17.
3
Scaling Pattern to Variations in Size during Development of the Vertebrate Neural Tube.脊椎动物神经管发育过程中尺寸变化的缩放模式。
Dev Cell. 2016 Apr 18;37(2):127-35. doi: 10.1016/j.devcel.2016.03.024.
4
Morphogen rules: design principles of gradient-mediated embryo patterning.形态发生素规则:梯度介导的胚胎模式形成的设计原则
Development. 2015 Dec 1;142(23):3996-4009. doi: 10.1242/dev.129452.
5
Ptch1 and Gli regulate Shh signalling dynamics via multiple mechanisms.Ptch1和Gli通过多种机制调节Shh信号传导动力学。
Nat Commun. 2015 Apr 2;6:6709. doi: 10.1038/ncomms7709.
6
Cranial nerve development requires co-ordinated Shh and canonical Wnt signaling.颅神经发育需要协调的 Sonic Hedgehog(Shh)信号和经典 Wnt 信号。
PLoS One. 2015 Mar 23;10(3):e0120821. doi: 10.1371/journal.pone.0120821. eCollection 2015.
7
A predictive model of bifunctional transcription factor signaling during embryonic tissue patterning.胚胎组织模式形成过程中双功能转录因子信号的预测模型。
Dev Cell. 2014 Nov 24;31(4):448-60. doi: 10.1016/j.devcel.2014.10.017.
8
Primary cilium and sonic hedgehog signaling during neural tube patterning: role of GPCRs and second messengers.神经管模式形成过程中的初级纤毛与音猬因子信号传导:G蛋白偶联受体和第二信使的作用
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9
Disrupting hedgehog and WNT signaling interactions promotes cleft lip pathogenesis.破坏 hedgehog 和 WNT 信号相互作用可促进唇裂的发病机制。
J Clin Invest. 2014 Apr;124(4):1660-71. doi: 10.1172/JCI72688. Epub 2014 Mar 3.
10
Molecular genetic control of cell patterning and fate determination in the developing ventral spinal cord.发育中的脊髓腹侧细胞模式形成和命运决定的分子遗传控制
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在没有来自底板的Shh活性梯度的情况下腹侧神经模式形成。

Ventral neural patterning in the absence of a Shh activity gradient from the floorplate.

作者信息

Iulianella Angelo, Sakai Daisuke, Kurosaka Hiroshi, Trainor Paul A

机构信息

Department of Medical Neuroscience, Faculty of Medicine, Dalhousie University, and Brain Repair Centre, Life Sciences Research Institute, Halifax, Nova Scotia, Canada.

Doshisha University, Graduate School of Brain Science, Kyotanabe, Kyoto, Japan.

出版信息

Dev Dyn. 2018 Jan;247(1):170-184. doi: 10.1002/dvdy.24590. Epub 2017 Oct 17.

DOI:10.1002/dvdy.24590
PMID:28891097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5739940/
Abstract

BACKGROUND

Vertebrate spinal cord development requires Sonic Hedgehog (Shh) signaling from the floorplate and notochord, where it is thought to act in concentration dependent manner to pattern distinct cell identities along the ventral-to-dorsal axis. While in vitro experiments demonstrate naïve neural tissues are sensitive to small changes in Shh levels, genetic studies illustrate that some degree of ventral patterning can occur despite significant perturbations in Shh signaling. Consequently, the mechanistic relationship between Shh morphogen levels and acquisition of distinct cell identities remains unclear.

RESULTS

We addressed this using Hedgehog acetyltransferase (Hhat ) and Wiggable mouse mutants. Hhat encodes a palmitoylase required for the secretion of Hedgehog proteins and formation of the Shh gradient. In its absence, the spinal cord develops without floorplate cells and V3 interneurons. Wiggable is an allele of the Shh receptor Patched1 (Ptch1 ) that is unable to inhibit Shh signal transduction, resulting in expanded ventral progenitor domains. Surprisingly, Hhat ; Ptch1 double mutants displayed fully restored ventral patterning despite an absence of Shh secretion from the floorplate.

CONCLUSIONS

The full range of neuronal progenitor types can be generated in the absence of a Shh gradient provided pathway repression is dampened, illustrating the complexity of morphogen dynamics in vertebrate patterning. Developmental Dynamics 247:170-184, 2018. © 2017 Wiley Periodicals, Inc.

摘要

背景

脊椎动物脊髓发育需要来自底板和脊索的音猬因子(Shh)信号,据认为该信号以浓度依赖方式起作用,沿腹侧到背侧轴形成不同的细胞身份模式。虽然体外实验表明未分化的神经组织对Shh水平的微小变化敏感,但遗传学研究表明,尽管Shh信号存在显著扰动,仍会发生一定程度的腹侧模式形成。因此,Shh形态发生素水平与不同细胞身份获得之间的机制关系仍不清楚。

结果

我们使用刺猬乙酰转移酶(Hhat)和摇摆小鼠突变体来解决这个问题。Hhat编码一种棕榈酰化酶,该酶是刺猬因子蛋白分泌和Shh梯度形成所必需的。在其缺失的情况下,脊髓发育时没有底板细胞和V3中间神经元。摇摆是Shh受体Patched1(Ptch1)的一个等位基因,它无法抑制Shh信号转导,导致腹侧祖细胞结构域扩大。令人惊讶的是,尽管底板没有分泌Shh,Hhat;Ptch1双突变体仍显示出完全恢复的腹侧模式形成。

结论

如果通路抑制减弱,在没有Shh梯度的情况下也可以产生完整范围的神经元祖细胞类型,这说明了脊椎动物模式形成中形态发生素动力学的复杂性。《发育动力学》247:170 - 184,2018年。©2017威利期刊公司。