adam10启动的Notch胞内结构域释放调控皮层神经元微管稳定性和径向迁移

Zhi Yang, Peng Li, Ren-Chao Chen, Jie Wang, Shaoran Wang, Ya Shen, Xiaohui Wu, B. Fang, Xuewen Cheng, Z. Xiong
{"title":"adam10启动的Notch胞内结构域释放调控皮层神经元微管稳定性和径向迁移","authors":"Zhi Yang, Peng Li, Ren-Chao Chen, Jie Wang, Shaoran Wang, Ya Shen, Xiaohui Wu, B. Fang, Xuewen Cheng, Z. Xiong","doi":"10.1093/cercor/bhx006","DOIUrl":null,"url":null,"abstract":"Abstract Proper neuronal migration is orchestrated by combined membrane signal paradigms, whereas the role and mechanism of regulated intramembrane proteolysis (RIP) remain to be illustrated. We show here that the disintegrin and metalloprotease‐domain containing protein 10 (ADAM10) regulates cortical neurons migration by initiating the RIP of Notch. We found that Notch intracellular domain (NICD) significantly rescued the migration defect of ADAM10‐deficient neurons. Moreover, ADAM10 deficiency led to reduced neuronal motility and disrupted microtubule (MT) structure, which were associated with downregulated expression of acetylated tubulin and MT‐associated proteins. Specifically, the NICD/RBPJ complex bound directly to the promoter, and regulated the neuronal expression level of doublecortin (DCX), a modulator of the MT cytoskeleton. Functionally, DCX overexpression largely restored neuron motility and reversed migration defect caused by ADAM10 knockout. Taken together, these findings demonstrate the direct requirement of ADAM10 in cortical radial migration and reveal the underlying mechanism by linking ADAM10‐initiated RIP of Notch to the regulation of MT cytoskeleton through transcriptional control of Dcx expression.","PeriodicalId":9825,"journal":{"name":"Cerebral Cortex (New York, NY)","volume":"31 1","pages":"919 - 932"},"PeriodicalIF":0.0000,"publicationDate":"2017-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"12","resultStr":"{\"title\":\"ADAM10-Initiated Release of Notch Intracellular Domain Regulates Microtubule Stability and Radial Migration of Cortical Neurons\",\"authors\":\"Zhi Yang, Peng Li, Ren-Chao Chen, Jie Wang, Shaoran Wang, Ya Shen, Xiaohui Wu, B. Fang, Xuewen Cheng, Z. Xiong\",\"doi\":\"10.1093/cercor/bhx006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Proper neuronal migration is orchestrated by combined membrane signal paradigms, whereas the role and mechanism of regulated intramembrane proteolysis (RIP) remain to be illustrated. We show here that the disintegrin and metalloprotease‐domain containing protein 10 (ADAM10) regulates cortical neurons migration by initiating the RIP of Notch. We found that Notch intracellular domain (NICD) significantly rescued the migration defect of ADAM10‐deficient neurons. Moreover, ADAM10 deficiency led to reduced neuronal motility and disrupted microtubule (MT) structure, which were associated with downregulated expression of acetylated tubulin and MT‐associated proteins. Specifically, the NICD/RBPJ complex bound directly to the promoter, and regulated the neuronal expression level of doublecortin (DCX), a modulator of the MT cytoskeleton. Functionally, DCX overexpression largely restored neuron motility and reversed migration defect caused by ADAM10 knockout. Taken together, these findings demonstrate the direct requirement of ADAM10 in cortical radial migration and reveal the underlying mechanism by linking ADAM10‐initiated RIP of Notch to the regulation of MT cytoskeleton through transcriptional control of Dcx expression.\",\"PeriodicalId\":9825,\"journal\":{\"name\":\"Cerebral Cortex (New York, NY)\",\"volume\":\"31 1\",\"pages\":\"919 - 932\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"12\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cerebral Cortex (New York, NY)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/cercor/bhx006\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cerebral Cortex (New York, NY)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/cercor/bhx006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12

摘要

适当的神经元迁移是由联合膜信号范式精心安排的,而调节膜内蛋白水解(RIP)的作用和机制仍有待阐明。我们在这里发现含有分解素和金属蛋白酶结构域的蛋白10 (ADAM10)通过启动Notch的RIP来调节皮质神经元的迁移。我们发现Notch胞内结构域(NICD)显著地修复了ADAM10‐缺陷神经元的迁移缺陷。此外,ADAM10缺乏导致神经元运动减少和微管(MT)结构破坏,这与乙酰化微管蛋白和MT相关蛋白的表达下调有关。具体来说,NICD/RBPJ复合物直接结合到启动子上,并调节MT细胞骨架调节剂双皮质素(DCX)的神经元表达水平。功能上,DCX过表达在很大程度上恢复了神经元的运动能力,逆转了ADAM10基因敲除引起的迁移缺陷。综上所述,这些发现证明了ADAM10在皮质径向迁移中的直接要求,并揭示了ADAM10通过转录控制Dcx表达将Notch的RIP与MT细胞骨架的调节联系起来的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ADAM10-Initiated Release of Notch Intracellular Domain Regulates Microtubule Stability and Radial Migration of Cortical Neurons
Abstract Proper neuronal migration is orchestrated by combined membrane signal paradigms, whereas the role and mechanism of regulated intramembrane proteolysis (RIP) remain to be illustrated. We show here that the disintegrin and metalloprotease‐domain containing protein 10 (ADAM10) regulates cortical neurons migration by initiating the RIP of Notch. We found that Notch intracellular domain (NICD) significantly rescued the migration defect of ADAM10‐deficient neurons. Moreover, ADAM10 deficiency led to reduced neuronal motility and disrupted microtubule (MT) structure, which were associated with downregulated expression of acetylated tubulin and MT‐associated proteins. Specifically, the NICD/RBPJ complex bound directly to the promoter, and regulated the neuronal expression level of doublecortin (DCX), a modulator of the MT cytoskeleton. Functionally, DCX overexpression largely restored neuron motility and reversed migration defect caused by ADAM10 knockout. Taken together, these findings demonstrate the direct requirement of ADAM10 in cortical radial migration and reveal the underlying mechanism by linking ADAM10‐initiated RIP of Notch to the regulation of MT cytoskeleton through transcriptional control of Dcx expression.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Consistently increased dorsolateral prefrontal cortex activity during the exposure to acute stressors Conditioning and pseudoconditioning differently change intrinsic excitability of inhibitory interneurons in the neocortex Phonological properties of logographic words modulate brain activation in bilinguals: a comparative study of Chinese characters and Japanese Kanji Inferior parietal cortex represents relational structures for explicit transitive inference In vivo ephaptic coupling allows memory network formation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1