Role of spinal astrocytes through the perisynaptic astrocytic process in pathological pain

IF 3.3 3区 医学 Q2 NEUROSCIENCES Molecular Brain Pub Date : 2023-12-13 DOI:10.1186/s13041-023-01069-z
Hyoung-Gon Ko, Heejung Chun, Seunghyo Han, Bong-Kiun Kaang
{"title":"Role of spinal astrocytes through the perisynaptic astrocytic process in pathological pain","authors":"Hyoung-Gon Ko, Heejung Chun, Seunghyo Han, Bong-Kiun Kaang","doi":"10.1186/s13041-023-01069-z","DOIUrl":null,"url":null,"abstract":"Pathological pain is caused by abnormal activity in the neural circuit that transmits nociceptive stimuli. Beyond homeostatic functions, astrocytes actively participate in regulating synaptic transmission as members of tripartite synapses. The perisynaptic astrocytic process (PAP) is the key structure that allows astrocytes to play these roles and not only physically supports synapse formation through cell adhesion molecules (CAMs) but also regulates the efficiency of chemical signaling. Accumulating evidence has revealed that spinal astrocytes are involved in pathological pain by modulating the efficacy of neurotransmitters such as glutamate and GABA through transporters located in the PAP and by directly regulating synaptic transmission through various gliotransmitters. Although various CAMs contribute to pathological pain, insufficient evidence is available as to whether astrocytic CAMs also have this role. Therefore, more in-depth research is needed on how pathological pain is induced and maintained by astrocytes, especially in the PAP surrounding the synapse, and this will subsequently increase our understanding and treatment of pathological pain.","PeriodicalId":18851,"journal":{"name":"Molecular Brain","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Brain","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13041-023-01069-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Pathological pain is caused by abnormal activity in the neural circuit that transmits nociceptive stimuli. Beyond homeostatic functions, astrocytes actively participate in regulating synaptic transmission as members of tripartite synapses. The perisynaptic astrocytic process (PAP) is the key structure that allows astrocytes to play these roles and not only physically supports synapse formation through cell adhesion molecules (CAMs) but also regulates the efficiency of chemical signaling. Accumulating evidence has revealed that spinal astrocytes are involved in pathological pain by modulating the efficacy of neurotransmitters such as glutamate and GABA through transporters located in the PAP and by directly regulating synaptic transmission through various gliotransmitters. Although various CAMs contribute to pathological pain, insufficient evidence is available as to whether astrocytic CAMs also have this role. Therefore, more in-depth research is needed on how pathological pain is induced and maintained by astrocytes, especially in the PAP surrounding the synapse, and this will subsequently increase our understanding and treatment of pathological pain.
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
脊髓星形胶质细胞通过突触周围星形胶质细胞过程在病理性疼痛中的作用
病理性疼痛是由传递痛觉刺激的神经回路活动异常引起的。除了稳态功能外,星形胶质细胞还作为三方突触的成员积极参与调节突触传递。突触周围星形胶质细胞过程(PAP)是星形胶质细胞发挥这些作用的关键结构,它不仅通过细胞粘附分子(CAM)在物理上支持突触的形成,还能调节化学信号的效率。越来越多的证据表明,脊髓星形胶质细胞通过位于 PAP 中的转运体调节谷氨酸和 GABA 等神经递质的功效,并通过各种神经胶质递质直接调节突触传递,从而参与病理性疼痛。虽然各种 CAMs 会导致病理性疼痛,但关于星形胶质细胞 CAMs 是否也具有这种作用,目前还没有足够的证据。因此,我们需要对星形胶质细胞如何诱导和维持病理性疼痛进行更深入的研究,尤其是在突触周围的 PAP 中,这将加深我们对病理性疼痛的理解和治疗。
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
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
期刊最新文献
Circadian cilia transcriptome in mouse brain across physiological and pathological states. TRPM4 inhibition slows neuritogenesis progression of cortical neurons Simulated weightlessness procedure, head-down bed rest has reversible effects on the metabolism of rhesus macaque. Absence of ATG9A and synaptophysin demixing on Rab5 mutation-induced giant endosomes. Electroacupuncture reduces inflammatory damage following cerebral ischemia-reperfusion by enhancing ABCA1-mediated efferocytosis in M2 microglia.
×
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