• 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

急性引入磷酸化丝氨酸129α-突触核蛋白会导致七鳃鳗突触处的线粒体严重肿胀。

Acute introduction of phosphoserine-129 α-synuclein induces severe swelling of mitochondria at lamprey synapses.

作者信息

Casiano Rivera Caroline V, Wallace Jaqulin N, Fisher Gia E, Morgan Jennifer R

机构信息

Eugene Bell Center for Regenerative Biology and Tissue Engineering, Marine Biological Laboratory, Woods Hole, Massachusetts, United States.

Biological Sciences Division, The University of Chicago.

出版信息

MicroPubl Biol. 2024 May 23;2024. doi: 10.17912/micropub.biology.001206. eCollection 2024.

DOI:10.17912/micropub.biology.001206
PMID:38854632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11157340/
Abstract

Abnormal synaptic aggregation of α-synuclein is linked to cognitive deficits in Parkinson's disease (PD). While the impacts of excess α-synuclein on synaptic function are well established, comparatively less is known about the effects on local mitochondria. Here, we examined morphological features of synaptic mitochondria treated with wild type (WT) or phosphoserine 129 (pS129) α-synuclein, a variant with prominent synaptic accumulation in PD. Acute introduction of pS129 α-synuclein to lamprey synapses caused an activity-dependent swelling and bursting of mitochondria, which did not occur with WT α-synuclein. These pS129-induced effects on mitochondria likely contribute to the synaptic deficits observed in PD.

摘要

α-突触核蛋白的异常突触聚集与帕金森病(PD)的认知缺陷有关。虽然过量的α-突触核蛋白对突触功能的影响已得到充分证实,但对局部线粒体的影响相对了解较少。在这里,我们研究了用野生型(WT)或丝氨酸129磷酸化(pS129)α-突触核蛋白处理的突触线粒体的形态特征,pS129α-突触核蛋白是一种在PD中具有突出突触积累的变体。将pS129α-突触核蛋白急性引入七鳃鳗突触会导致线粒体的活性依赖性肿胀和破裂,而WTα-突触核蛋白则不会出现这种情况。这些pS129对线粒体的诱导作用可能导致了PD中观察到的突触缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e89/11157340/408eed91385b/25789430-2024-micropub.biology.001206.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e89/11157340/408eed91385b/25789430-2024-micropub.biology.001206.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e89/11157340/408eed91385b/25789430-2024-micropub.biology.001206.jpg

相似文献

1
Acute introduction of phosphoserine-129 α-synuclein induces severe swelling of mitochondria at lamprey synapses.急性引入磷酸化丝氨酸129α-突触核蛋白会导致七鳃鳗突触处的线粒体严重肿胀。
MicroPubl Biol. 2024 May 23;2024. doi: 10.17912/micropub.biology.001206. eCollection 2024.
2
Excess phosphoserine-129 α-synuclein induces synaptic vesicle trafficking and declustering defects at a vertebrate synapse.过量磷酸丝氨酸-129α-突触核蛋白在脊椎动物突触诱导突触囊泡运输和去簇缺陷。
Mol Biol Cell. 2024 Jan 1;35(1):ar10. doi: 10.1091/mbc.E23-07-0269. Epub 2023 Nov 22.
3
Hsc70 Ameliorates the Vesicle Recycling Defects Caused by Excess α-Synuclein at Synapses.Hsc70 改善突触处过量 α-突触核蛋白引起的囊泡再循环缺陷。
eNeuro. 2020 Jan 31;7(1). doi: 10.1523/ENEURO.0448-19.2020. Print 2020 Jan/Feb.
4
A53T Mutant Alpha-Synuclein Induces Tau-Dependent Postsynaptic Impairment Independently of Neurodegenerative Changes.A53T 突变型 α-突触核蛋白独立于神经退行性变化诱导 Tau 依赖性突触后损伤。
J Neurosci. 2018 Nov 7;38(45):9754-9767. doi: 10.1523/JNEUROSCI.0344-18.2018. Epub 2018 Sep 24.
5
Plasma pS129-α-Synuclein Is a Surrogate Biofluid Marker of Motor Severity and Progression in Parkinson's Disease.血浆磷酸化丝氨酸129α-突触核蛋白是帕金森病运动严重程度和病情进展的替代生物流体标志物。
J Clin Med. 2019 Oct 3;8(10):1601. doi: 10.3390/jcm8101601.
6
Effects of Excess Brain-Derived Human α-Synuclein on Synaptic Vesicle Trafficking.过量人脑源性α-突触核蛋白对突触小泡运输的影响。
Front Neurosci. 2021 Feb 4;15:639414. doi: 10.3389/fnins.2021.639414. eCollection 2021.
7
Dynamic reversibility of α-synuclein serine-129 phosphorylation is impaired in synucleinopathy models.α-突触核蛋白丝氨酸 129 磷酸化的动态可逆性在突触核蛋白病模型中受损。
EMBO Rep. 2023 Dec 6;24(12):e57145. doi: 10.15252/embr.202357145. Epub 2023 Oct 23.
8
Enhanced Susceptibility of PINK1 Knockout Rats to α-Synuclein Fibrils.PINK1基因敲除大鼠对α-突触核蛋白原纤维的易感性增强。
Neuroscience. 2020 Jun 15;437:64-75. doi: 10.1016/j.neuroscience.2020.04.032. Epub 2020 Apr 27.
9
α-Synuclein phosphorylation at serine 129 occurs after initial protein deposition and inhibits seeded fibril formation and toxicity.α-突触核蛋白在丝氨酸 129 的磷酸化发生在初始蛋白沉积之后,并抑制种子纤维形成和毒性。
Proc Natl Acad Sci U S A. 2022 Apr 12;119(15):e2109617119. doi: 10.1073/pnas.2109617119. Epub 2022 Mar 30.
10
α-Synuclein Dimers Impair Vesicle Fission during Clathrin-Mediated Synaptic Vesicle Recycling.α-突触核蛋白二聚体在网格蛋白介导的突触小泡循环过程中损害小泡裂变。
Front Cell Neurosci. 2017 Dec 11;11:388. doi: 10.3389/fncel.2017.00388. eCollection 2017.

本文引用的文献

1
Serine-129 phosphorylation of α-synuclein is an activity-dependent trigger for physiologic protein-protein interactions and synaptic function.α-突触核蛋白丝氨酸 129 磷酸化是一种依赖活性的触发因素,可导致生理性蛋白-蛋白相互作用和突触功能。
Neuron. 2023 Dec 20;111(24):4006-4023.e10. doi: 10.1016/j.neuron.2023.11.020.
2
Excess phosphoserine-129 α-synuclein induces synaptic vesicle trafficking and declustering defects at a vertebrate synapse.过量磷酸丝氨酸-129α-突触核蛋白在脊椎动物突触诱导突触囊泡运输和去簇缺陷。
Mol Biol Cell. 2024 Jan 1;35(1):ar10. doi: 10.1091/mbc.E23-07-0269. Epub 2023 Nov 22.
3
Dynamic physiological α-synuclein S129 phosphorylation is driven by neuronal activity.
动态生理性α-突触核蛋白S129磷酸化由神经元活动驱动。
NPJ Parkinsons Dis. 2023 Jan 16;9(1):4. doi: 10.1038/s41531-023-00444-w.
4
α-Synuclein in synaptic function and dysfunction.α-突触核蛋白在突触功能及功能障碍中的作用。
Trends Neurosci. 2023 Feb;46(2):153-166. doi: 10.1016/j.tins.2022.11.007. Epub 2022 Dec 23.
5
Pathological structural conversion of α-synuclein at the mitochondria induces neuronal toxicity.α-突触核蛋白在线粒体中的病理性结构转换诱导神经元毒性。
Nat Neurosci. 2022 Sep;25(9):1134-1148. doi: 10.1038/s41593-022-01140-3. Epub 2022 Aug 30.
6
Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson's Disease.α-突触核蛋白与脂质的相互作用:线粒体心磷脂在帕金森病发病机制中扮演关键角色。
Front Neurosci. 2020 Oct 6;14:578993. doi: 10.3389/fnins.2020.578993. eCollection 2020.
7
Hsc70 Ameliorates the Vesicle Recycling Defects Caused by Excess α-Synuclein at Synapses.Hsc70 改善突触处过量 α-突触核蛋白引起的囊泡再循环缺陷。
eNeuro. 2020 Jan 31;7(1). doi: 10.1523/ENEURO.0448-19.2020. Print 2020 Jan/Feb.
8
Cardiolipin Promotes Pore-Forming Activity of Alpha-Synuclein Oligomers in Mitochondrial Membranes.心磷脂促进α-突触核蛋白寡聚体在线粒体膜中形成孔道。
ACS Chem Neurosci. 2019 Aug 21;10(8):3815-3829. doi: 10.1021/acschemneuro.9b00320. Epub 2019 Aug 6.
9
The physiological role of α-synuclein and its relationship to Parkinson's Disease.α-突触核蛋白的生理作用及其与帕金森病的关系。
J Neurochem. 2019 Sep;150(5):475-486. doi: 10.1111/jnc.14810. Epub 2019 Jul 28.
10
Lewy pathology in Parkinson's disease consists of crowded organelles and lipid membranes.路易体病理存在于帕金森病中,由挤在一起的细胞器和脂膜组成。
Nat Neurosci. 2019 Jul;22(7):1099-1109. doi: 10.1038/s41593-019-0423-2. Epub 2019 Jun 24.