• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

线粒体 OPA1 缺乏与成年神经发生相关的空间记忆可逆缺陷有关。

Mitochondrial OPA1 Deficiency Is Associated to Reversible Defects in Spatial Memory Related to Adult Neurogenesis in Mice.

机构信息

Centre de Recherches sur la Cognition Animale (CRCA), Centre de Biologie Intégrative (CBI), Université de Toulouse, Centre National de la Recherche Scientifique, Université Toulouse 3, 31400, Toulouse, France.

Department of Medical Physiology and Biophysics, Faculty of Medicine, Universitas Indonesia, Jakarta 10430, Indonesia.

出版信息

eNeuro. 2023 Nov 20;10(11). doi: 10.1523/ENEURO.0073-23.2023. Print 2023 Nov.

DOI:10.1523/ENEURO.0073-23.2023
PMID:37863658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10668243/
Abstract

Mitochondria are integrative hubs central to cellular adaptive pathways. Such pathways are critical in highly differentiated postmitotic neurons, the plasticity of which sustains brain function. Consequently, defects in mitochondria and in their dynamics appear instrumental in neurodegenerative diseases and may also participate in cognitive impairments. To directly test this hypothesis, we analyzed cognitive performances in a mouse mitochondria-based disease model, because of haploinsufficiency in the mitochondrial optic atrophy type 1 (OPA1) protein involved in mitochondrial dynamics. In males, we evaluated adult hippocampal neurogenesis parameters using immunohistochemistry. We performed a battery of tests to assess basal behavioral characteristics and cognitive performances, and tested putative treatments. While in dominant optic atrophy (DOA) mouse models, the known main symptoms are late onset visual deficits, we discovered early impairments in hippocampus-dependent spatial memory attributable to defects in adult neurogenesis. Moreover, less connected adult-born hippocampal neurons showed a decrease in mitochondrial content. Remarkably, voluntary exercise or pharmacological treatment targeting mitochondrial dynamics restored spatial memory in DOA mice. Altogether, our study identifies a crucial role for OPA1-dependent mitochondrial functions in adult neurogenesis, and thus in hippocampal-dependent cognitive functions. More generally, our findings show that adult neurogenesis is highly sensitive to mild mitochondrial defects, generating impairments in spatial memory that can be detected at an early stage and counterbalanced by physical exercise and pharmacological targeting of mitochondrial dynamics. Thus, amplification of mitochondrial function at an early stage appears beneficial for late-onset neurodegenerative diseases.

摘要

线粒体是细胞适应途径的综合中心。这些途径在高度分化的有丝分裂后神经元中至关重要,其可塑性维持着大脑功能。因此,线粒体及其动态的缺陷似乎在神经退行性疾病中起着重要作用,也可能参与认知障碍。为了直接验证这一假说,我们分析了一种基于线粒体的小鼠疾病模型的认知表现,因为参与线粒体动态的线粒体视神经萎缩 1 型(OPA1)蛋白的单倍体不足。在雄性中,我们使用免疫组织化学分析评估成年海马神经发生参数。我们进行了一系列测试来评估基础行为特征和认知表现,并测试了潜在的治疗方法。虽然在显性视神经萎缩(DOA)小鼠模型中,已知的主要症状是视觉障碍,但我们发现由于成年神经发生缺陷,海马依赖性空间记忆出现早期损伤。此外,连接较少的成年新生海马神经元的线粒体含量减少。值得注意的是,针对线粒体动力学的自愿运动或药物治疗可恢复 DOA 小鼠的空间记忆。总之,我们的研究确定了 OPA1 依赖性线粒体功能在成年神经发生中的关键作用,从而在海马依赖性认知功能中起关键作用。更普遍地说,我们的研究结果表明,成年神经发生对轻微的线粒体缺陷高度敏感,导致空间记忆受损,可在早期检测到,并可通过体育锻炼和靶向线粒体动力学的药物治疗来平衡。因此,早期放大线粒体功能似乎对晚期神经退行性疾病有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/1b827948fb5f/ENEURO.0073-23.2023_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/578127e58195/ENEURO.0073-23.2023_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/d376260a0b5f/ENEURO.0073-23.2023_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/288df2df4a4d/ENEURO.0073-23.2023_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/d52b05852a34/ENEURO.0073-23.2023_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/1b827948fb5f/ENEURO.0073-23.2023_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/578127e58195/ENEURO.0073-23.2023_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/d376260a0b5f/ENEURO.0073-23.2023_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/288df2df4a4d/ENEURO.0073-23.2023_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/d52b05852a34/ENEURO.0073-23.2023_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/170c/10668243/1b827948fb5f/ENEURO.0073-23.2023_f005.jpg

相似文献

1
Mitochondrial OPA1 Deficiency Is Associated to Reversible Defects in Spatial Memory Related to Adult Neurogenesis in Mice.线粒体 OPA1 缺乏与成年神经发生相关的空间记忆可逆缺陷有关。
eNeuro. 2023 Nov 20;10(11). doi: 10.1523/ENEURO.0073-23.2023. Print 2023 Nov.
2
OPA1 haploinsufficiency induces a BNIP3-dependent decrease in mitophagy in neurons: relevance to Dominant Optic Atrophy.OPA1单倍剂量不足导致神经元线粒体自噬中BNIP3依赖的减少:与显性遗传性视神经萎缩的相关性
J Neurochem. 2017 Feb;140(3):485-494. doi: 10.1111/jnc.13894. Epub 2016 Dec 20.
3
Loss of prohibitin membrane scaffolds impairs mitochondrial architecture and leads to tau hyperphosphorylation and neurodegeneration.抑素膜支架的丧失会损害线粒体的结构,导致过度磷酸化的 tau 蛋白积聚和神经退行性变。
PLoS Genet. 2012;8(11):e1003021. doi: 10.1371/journal.pgen.1003021. Epub 2012 Nov 8.
4
Dominant optic atrophy: Culprit mitochondria in the optic nerve.显性视神经萎缩:视神经中的罪魁祸首——线粒体。
Prog Retin Eye Res. 2021 Jul;83:100935. doi: 10.1016/j.preteyeres.2020.100935. Epub 2020 Dec 17.
5
Inhibition of Drp1-mediated mitochondrial fission improves mitochondrial dynamics and bioenergetics stimulating neurogenesis in hippocampal progenitor cells from a Down syndrome mouse model.抑制 Drp1 介导线粒体分裂可改善线粒体动力学和生物能量学,从而刺激唐氏综合征小鼠模型中海马祖细胞的神经发生。
Biochim Biophys Acta Mol Basis Dis. 2017 Dec;1863(12):3117-3127. doi: 10.1016/j.bbadis.2017.09.014. Epub 2017 Sep 20.
6
Optic atrophy 1 mediates mitochondria remodeling and dopaminergic neurodegeneration linked to complex I deficiency.视神经萎缩 1 介导与复合物 I 缺陷相关的线粒体重构和多巴胺能神经退行性变。
Cell Death Differ. 2013 Jan;20(1):77-85. doi: 10.1038/cdd.2012.95. Epub 2012 Aug 3.
7
Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiency.在显性视神经萎缩的Opa1(Q285STOP)小鼠模型中,线粒体功能障碍是由Opa1单倍剂量不足引起的。
Cell Death Dis. 2016 Jul 28;7(7):e2309. doi: 10.1038/cddis.2016.160.
8
OPA1: How much do we know to approach therapy?OPA1:我们对治疗方法了解多少?
Pharmacol Res. 2018 May;131:199-210. doi: 10.1016/j.phrs.2018.02.018. Epub 2018 Feb 15.
9
Amplifying mitochondrial function rescues adult neurogenesis in a mouse model of Alzheimer's disease.增强线粒体功能可挽救阿尔茨海默病小鼠模型中的成年神经发生。
Neurobiol Dis. 2017 Jun;102:113-124. doi: 10.1016/j.nbd.2017.03.002. Epub 2017 Mar 10.
10
Mitochondrial regulation of adult hippocampal neurogenesis: Insights into neurological function and neurodevelopmental disorders.线粒体对成年海马神经发生的调节:对神经功能和神经发育障碍的深入了解。
Neurobiol Dis. 2024 Sep;199:106604. doi: 10.1016/j.nbd.2024.106604. Epub 2024 Jul 11.

引用本文的文献

1
A High-Fat Diet Induces Oxidative Stress in OPA1 Mouse Cortices: A Critical Double Challenge.高脂饮食诱导OPA1小鼠皮质氧化应激:一项关键的双重挑战。
Antioxidants (Basel). 2025 Jul 17;14(7):876. doi: 10.3390/antiox14070876.
2
Early Life Exposure to Deltamethrin Impairs Synaptic Function by Altering the Brain-Derived Extracellular Vesicle Proteome.生命早期接触溴氰菊酯会通过改变脑源性细胞外囊泡蛋白质组来损害突触功能。
Mol Cell Proteomics. 2025 Feb;24(2):100902. doi: 10.1016/j.mcpro.2024.100902. Epub 2024 Dec 31.
3
Hippocampal mitophagy contributes to spatial memory via maintaining neurogenesis during the development of mice.

本文引用的文献

1
Dephosphorylation of ERK1/2 and DRP1 S585 regulates mitochondrial dynamics in glutamate toxicity of retinal neurons in vitro.ERK1/2 和 DRP1 S585 的去磷酸化调节体外谷氨酸诱导的视网膜神经元线粒体动力学。
Exp Eye Res. 2022 Dec;225:109271. doi: 10.1016/j.exer.2022.109271. Epub 2022 Oct 3.
2
Mitochondrial function and dynamics in neural stem cells and neurogenesis: Implications for neurodegenerative diseases.神经干细胞和神经发生中的线粒体功能和动态:对神经退行性疾病的影响。
Ageing Res Rev. 2022 Sep;80:101667. doi: 10.1016/j.arr.2022.101667. Epub 2022 Jun 15.
3
Metabolic control of adult neural stem cell self-renewal by the mitochondrial protease YME1L.
海马体的线粒体自噬通过在小鼠发育过程中维持神经发生来促进空间记忆。
CNS Neurosci Ther. 2024 Jun;30(6):e14800. doi: 10.1111/cns.14800.
线粒体蛋白酶 YME1L 对成体神经干细胞自我更新的代谢控制。
Cell Rep. 2022 Feb 15;38(7):110370. doi: 10.1016/j.celrep.2022.110370.
4
Mitochondrial function in development and disease.线粒体在发育和疾病中的功能。
Dis Model Mech. 2021 Jun 1;14(6). doi: 10.1242/dmm.048912. Epub 2021 Jun 11.
5
Mitochondrial OMA1 and OPA1 as Gatekeepers of Organellar Structure/Function and Cellular Stress Response.线粒体OMA1和OPA1作为细胞器结构/功能及细胞应激反应的守护者
Front Cell Dev Biol. 2021 Mar 25;9:626117. doi: 10.3389/fcell.2021.626117. eCollection 2021.
6
Mitochondria as Signaling Organelles Control Mammalian Stem Cell Fate.线粒体作为信号细胞器控制哺乳动物干细胞命运。
Cell Stem Cell. 2021 Mar 4;28(3):394-408. doi: 10.1016/j.stem.2021.02.011.
7
Intrinsic Mechanisms Regulating Neuronal Migration in the Postnatal Brain.调节出生后脑内神经元迁移的内在机制
Front Cell Neurosci. 2021 Jan 13;14:620379. doi: 10.3389/fncel.2020.620379. eCollection 2020.
8
Dominant optic atrophy: Culprit mitochondria in the optic nerve.显性视神经萎缩:视神经中的罪魁祸首——线粒体。
Prog Retin Eye Res. 2021 Jul;83:100935. doi: 10.1016/j.preteyeres.2020.100935. Epub 2020 Dec 17.
9
Tau accumulation in astrocytes of the dentate gyrus induces neuronal dysfunction and memory deficits in Alzheimer's disease.在阿尔茨海默病中,齿状回星形胶质细胞中的 Tau 积累会导致神经元功能障碍和记忆缺陷。
Nat Neurosci. 2020 Dec;23(12):1567-1579. doi: 10.1038/s41593-020-00728-x. Epub 2020 Nov 9.
10
OPA1 deficiency accelerates hippocampal synaptic remodelling and age-related deficits in learning and memory.OPA1 缺乏会加速海马体突触重塑以及与年龄相关的学习和记忆缺陷。
Brain Commun. 2020 Jul 15;2(2):fcaa101. doi: 10.1093/braincomms/fcaa101. eCollection 2020.