Progress of reprogramming astrocytes into neuron

IF 2.6 3区 医学 Q3 NEUROSCIENCES Molecular and Cellular Neuroscience Pub Date : 2024-06-10 DOI:10.1016/j.mcn.2024.103947
Sitong Liu , Ximing Xu , Emmanuel Omari-Siaw , Jiangnan Yu , Wenwen Deng
{"title":"Progress of reprogramming astrocytes into neuron","authors":"Sitong Liu ,&nbsp;Ximing Xu ,&nbsp;Emmanuel Omari-Siaw ,&nbsp;Jiangnan Yu ,&nbsp;Wenwen Deng","doi":"10.1016/j.mcn.2024.103947","DOIUrl":null,"url":null,"abstract":"<div><p>As the main players in the central nervous system (CNS), neurons dominate most life activities. However, after accidental trauma or neurodegenerative diseases, neurons are unable to regenerate themselves. The loss of this important role can seriously affect the quality of life of patients, ranging from movement disorders to disability and even death. There is no suitable treatment to prevent or reverse this process. Therefore, the regeneration of neurons after loss has been a major clinical problem and the key to treatment. Replacing the lost neurons by transdifferentiation of other cells is the only viable approach. Although much progress has been made in stem cell therapy, ethical issues, immune rejection, and limited cell sources still hinder its clinical application. In recent years, somatic cell reprogramming technology has brought a new dawn. Among them, astrocytes, as endogenously abundant cells homologous to neurons, have good potential and application value for reprogramming into neurons, having been reprogrammed into neurons <em>in vitro</em> and <em>in vivo</em> in a variety of ways.</p></div>","PeriodicalId":18739,"journal":{"name":"Molecular and Cellular Neuroscience","volume":"130 ","pages":"Article 103947"},"PeriodicalIF":2.6000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and Cellular Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1044743124000320","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

As the main players in the central nervous system (CNS), neurons dominate most life activities. However, after accidental trauma or neurodegenerative diseases, neurons are unable to regenerate themselves. The loss of this important role can seriously affect the quality of life of patients, ranging from movement disorders to disability and even death. There is no suitable treatment to prevent or reverse this process. Therefore, the regeneration of neurons after loss has been a major clinical problem and the key to treatment. Replacing the lost neurons by transdifferentiation of other cells is the only viable approach. Although much progress has been made in stem cell therapy, ethical issues, immune rejection, and limited cell sources still hinder its clinical application. In recent years, somatic cell reprogramming technology has brought a new dawn. Among them, astrocytes, as endogenously abundant cells homologous to neurons, have good potential and application value for reprogramming into neurons, having been reprogrammed into neurons in vitro and in vivo in a variety of ways.

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
将星形胶质细胞重编程为神经元的进展。
作为中枢神经系统(CNS)的主要角色,神经元主导着大多数生命活动。然而,在遭受意外创伤或患上神经退行性疾病后,神经元无法自我再生。失去这一重要作用会严重影响患者的生活质量,包括运动障碍、残疾甚至死亡。目前还没有合适的治疗方法来预防或逆转这一过程。因此,神经元缺失后的再生一直是一个重大的临床问题,也是治疗的关键。通过其他细胞的转分化来替代失去的神经元是唯一可行的方法。虽然干细胞治疗取得了很大进展,但伦理问题、免疫排斥和有限的细胞来源仍阻碍着干细胞的临床应用。近年来,体细胞重编程技术带来了新的曙光。其中,星形胶质细胞作为与神经元同源的内源性丰富细胞,在体外和体内通过多种方式重编程为神经元,具有很好的潜力和应用价值。
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
CiteScore
5.60
自引率
0.00%
发文量
65
审稿时长
37 days
期刊介绍: Molecular and Cellular Neuroscience publishes original research of high significance covering all aspects of neurosciences indicated by the broadest interpretation of the journal''s title. In particular, the journal focuses on synaptic maintenance, de- and re-organization, neuron-glia communication, and de-/regenerative neurobiology. In addition, studies using animal models of disease with translational prospects and experimental approaches with backward validation of disease signatures from human patients are welcome.
期刊最新文献
Potential key pathophysiological participant and treatment target in autism spectrum disorder: Microglia Sphingosine-1-phosphate receptor 3 promotes neuronal apoptosis via the TNF-α/caspase-3 signaling pathway after acute intracerebral hemorrhage The mRNA expression profile of glycine receptor subunits alpha 1, alpha 2, alpha 4 and beta in female and male mice. TAT-PPA1 protects against oxidative stress-induced loss of dopaminergic neurons Inhibition of phosphodiesterase 10A mitigates neuronal injury by modulating apoptotic pathways in cold-induced traumatic brain injury
×
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