How to make striatal projection neurons.

Neurogenesis (Austin, Tex.) Pub Date : 2015-12-15 eCollection Date: 2015-01-01 DOI:10.1080/23262133.2015.1100227
Marija Fjodorova, Zoe Noakes, Meng Li
{"title":"How to make striatal projection neurons.","authors":"Marija Fjodorova,&nbsp;Zoe Noakes,&nbsp;Meng Li","doi":"10.1080/23262133.2015.1100227","DOIUrl":null,"url":null,"abstract":"<p><p>Medium spiny neurons (MSNs) are the main projection neurons of the striatum and are preferentially lost in Huntington's disease (HD). With no current cure for this neurodegenerative disorder, the specificity of neuronal loss in the striatum makes cell transplantation therapy an attractive avenue for its treatment. Also, given that MSNs are particularly vulnerable in HD, it is necessary to understand why these neurons degenerate in order to develop new therapeutic options. Both approaches require access to human MSN progenitors and their mature neuronal derivatives. Human embryonic stem cells and HD patient induced pluripotent stem cells (together referred to as hPSCs) may serve as an unlimited source of such tissue if they can be directed toward authentic striatal neuronal lineage. Understanding the MSN differentiation pathway in the brain is therefore of paramount importance for the generation of accurate protocols to obtain striatal cells in vitro. The focus of this mini review will be on striatal development and current methods to generate MSNs from hPSCs. </p>","PeriodicalId":74274,"journal":{"name":"Neurogenesis (Austin, Tex.)","volume":" ","pages":"e1100227"},"PeriodicalIF":0.0000,"publicationDate":"2015-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23262133.2015.1100227","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurogenesis (Austin, Tex.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23262133.2015.1100227","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15

Abstract

Medium spiny neurons (MSNs) are the main projection neurons of the striatum and are preferentially lost in Huntington's disease (HD). With no current cure for this neurodegenerative disorder, the specificity of neuronal loss in the striatum makes cell transplantation therapy an attractive avenue for its treatment. Also, given that MSNs are particularly vulnerable in HD, it is necessary to understand why these neurons degenerate in order to develop new therapeutic options. Both approaches require access to human MSN progenitors and their mature neuronal derivatives. Human embryonic stem cells and HD patient induced pluripotent stem cells (together referred to as hPSCs) may serve as an unlimited source of such tissue if they can be directed toward authentic striatal neuronal lineage. Understanding the MSN differentiation pathway in the brain is therefore of paramount importance for the generation of accurate protocols to obtain striatal cells in vitro. The focus of this mini review will be on striatal development and current methods to generate MSNs from hPSCs.

Abstract Image

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
如何制造纹状体投射神经元。
中棘神经元(MSNs)是纹状体的主要投射神经元,在亨廷顿病(HD)中优先丢失。由于目前还没有治愈这种神经退行性疾病的方法,纹状体中神经元丢失的特异性使得细胞移植治疗成为一种有吸引力的治疗途径。此外,考虑到msnn在HD中特别脆弱,为了开发新的治疗方案,有必要了解这些神经元退化的原因。这两种方法都需要获得人类MSN祖细胞及其成熟的神经元衍生物。人类胚胎干细胞和亨廷顿舞蹈症患者诱导的多能干细胞(统称为hPSCs)可以作为这种组织的无限来源,如果它们能够定向到真正的纹状体神经元谱系。因此,了解大脑中MSN的分化途径对于在体外获得纹状体细胞的准确方案的生成至关重要。本文将重点介绍纹状体的发育和目前从造血干细胞中生成骨髓间充质干细胞的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Role of neoblasts in the patterned postembryonic growth of the platyhelminth Macrostomum lignano. There's no place like home - HGF-c-MET signaling and melanocyte migration into the mammalian cochlea Effects of Isx-9 and stress on adult hippocampal neurogenesis: Experimental considerations and future perspectives. Opportunities lost and gained: Changes in progenitor competence during nervous system development. Endogenous Brain Repair: Overriding intrinsic lineage determinates through injury-induced micro-environmental signals.
×
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