Astrocytes release ATP/ADP and glutamate in flashes via vesicular exocytosis

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-11-22 DOI:10.1038/s41380-024-02851-8
Heng Li, Yuqing Zhao, Ruicheng Dai, Peiyao Geng, Danwei Weng, Wenting Wu, Fengting Yu, Rui Lin, Zhaofa Wu, Yulong Li, Minmin Luo
{"title":"Astrocytes release ATP/ADP and glutamate in flashes via vesicular exocytosis","authors":"Heng Li, Yuqing Zhao, Ruicheng Dai, Peiyao Geng, Danwei Weng, Wenting Wu, Fengting Yu, Rui Lin, Zhaofa Wu, Yulong Li, Minmin Luo","doi":"10.1038/s41380-024-02851-8","DOIUrl":null,"url":null,"abstract":"<p>Astrocytes regulate brain functions through gliotransmitters like ATP/ADP and glutamate, but their release patterns and mechanisms remain controversial. Here, we visualized ATP/ADP and glutamate response following astrocyte activation and investigated their mechanisms in vivo. Employing cOpn5-mediated optogenetic stimulation, genetically encoded fluorescent sensors, and two-photon imaging, we observed ATP/ADP released as temporally prolonged and spatially extended flashes that later converted to adenosine. This release occurs via Ca<sup>2+</sup> and VNUT-dependent vesicular exocytosis. Additionally, astrocytes also release glutamate in flashes through TeNT-sensitive exocytosis, independent of ATP/ADP release. ATP/ADP released by astrocytes triggers further ATP/ADP release from microglia through P2Y12- and VNUT-dependent mechanisms. VNUT in astrocytes and microglia also contributes to ATP/ADP release under LPS-induced brain inflammation. These findings establish Ca<sup>2+</sup>-dependent vesicular exocytosis as a key mode of action, reveal intricate astrocyte-microglia interactions, and suggest a role for gliotransmission in brain inflammation. Furthermore, the methodologies may provide valuable tools for deciphering glial physiology and pathophysiology.</p>","PeriodicalId":19008,"journal":{"name":"Molecular Psychiatry","volume":"24 1","pages":""},"PeriodicalIF":9.6000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41380-024-02851-8","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Astrocytes regulate brain functions through gliotransmitters like ATP/ADP and glutamate, but their release patterns and mechanisms remain controversial. Here, we visualized ATP/ADP and glutamate response following astrocyte activation and investigated their mechanisms in vivo. Employing cOpn5-mediated optogenetic stimulation, genetically encoded fluorescent sensors, and two-photon imaging, we observed ATP/ADP released as temporally prolonged and spatially extended flashes that later converted to adenosine. This release occurs via Ca2+ and VNUT-dependent vesicular exocytosis. Additionally, astrocytes also release glutamate in flashes through TeNT-sensitive exocytosis, independent of ATP/ADP release. ATP/ADP released by astrocytes triggers further ATP/ADP release from microglia through P2Y12- and VNUT-dependent mechanisms. VNUT in astrocytes and microglia also contributes to ATP/ADP release under LPS-induced brain inflammation. These findings establish Ca2+-dependent vesicular exocytosis as a key mode of action, reveal intricate astrocyte-microglia interactions, and suggest a role for gliotransmission in brain inflammation. Furthermore, the methodologies may provide valuable tools for deciphering glial physiology and pathophysiology.

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
星形胶质细胞通过泡状外渗在闪烁中释放 ATP/ADP 和谷氨酸
星形胶质细胞通过 ATP/ADP 和谷氨酸等胶质递质调节大脑功能,但它们的释放模式和机制仍存在争议。在这里,我们观察了星形胶质细胞激活后的 ATP/ADP 和谷氨酸反应,并研究了它们在体内的机制。利用 cOpn5 介导的光遗传刺激、基因编码的荧光传感器和双光子成像,我们观察到 ATP/ADP 以时间延长、空间扩展的闪烁形式释放,随后转化为腺苷。这种释放是通过 Ca2+ 和 VNUT 依赖性囊泡外排发生的。此外,星形胶质细胞还通过 TeNT 敏感性外渗以闪烁方式释放谷氨酸,与 ATP/ADP 释放无关。星形胶质细胞释放的 ATP/ADP 通过 P2Y12 和 VNUT 依赖性机制进一步触发小胶质细胞释放 ATP/ADP。在 LPS 诱导的脑部炎症中,星形胶质细胞和小胶质细胞中的 VNUT 也有助于 ATP/ADP 的释放。这些发现确定了 Ca2+ 依赖性囊泡外泌是一种关键的作用模式,揭示了星形胶质细胞与小胶质细胞之间错综复杂的相互作用,并提示了胶质细胞传导在脑部炎症中的作用。此外,这些方法可为破译神经胶质生理学和病理生理学提供有价值的工具。
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 Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
期刊最新文献
Disruption of macroscale functional network organisation in patients with frontotemporal dementia Dopamine release and dopamine-related gene expression in the amygdala are modulated by the gastrin-releasing peptide in opposite directions during stress-enhanced fear learning and extinction Activation of somatostatin neurons in the medial amygdala reverses long-term aggression and social deficits associated to early-life stress in male mice Association between bullying victimization and obsessive-compulsive disorder: a population-based, genetically informative study A longitudinal study of hippocampal subfield volumes and hippocampal glutamate levels in antipsychotic-naïve first episode psychosis patients
×
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