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长时程增强(LTP)后,线粒体对持续的突触前囊泡动员的支持以及与年龄相关的突触生长。

Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP.

作者信息

Smith Heather L, Bourne Jennifer N, Cao Guan, Chirillo Michael A, Ostroff Linnaea E, Watson Deborah J, Harris Kristen M

机构信息

Department of Neuroscience, Center for Learning and Memory, Institute for Neuroscience, University of Texas at Austin, Austin, United States.

Department of Cell and Developmental Biology, University of Colorado Denver - Anschutz Medical Campus, Aurora, United States.

出版信息

Elife. 2016 Dec 19;5:e15275. doi: 10.7554/eLife.15275.

DOI:10.7554/eLife.15275
PMID:27991850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5235352/
Abstract

Mitochondria support synaptic transmission through production of ATP, sequestration of calcium, synthesis of glutamate, and other vital functions. Surprisingly, less than 50% of hippocampal CA1 presynaptic boutons contain mitochondria, raising the question of whether synapses without mitochondria can sustain changes in efficacy. To address this question, we analyzed synapses from postnatal day 15 (P15) and adult rat hippocampus that had undergone theta-burst stimulation to produce long-term potentiation (TBS-LTP) and compared them to control or no stimulation. At 30 and 120 min after TBS-LTP, vesicles were decreased only in presynaptic boutons that contained mitochondria at P15, and vesicle decrement was greatest in adult boutons containing mitochondria. Presynaptic mitochondrial cristae were widened, suggesting a sustained energy demand. Thus, mitochondrial proximity reflected enhanced vesicle mobilization well after potentiation reached asymptote, in parallel with the apparently silent addition of new dendritic spines at P15 or the silent enlargement of synapses in adults.

摘要

线粒体通过产生三磷酸腺苷(ATP)、隔离钙、合成谷氨酸以及其他重要功能来支持突触传递。令人惊讶的是,海马体CA1区不到50%的突触前终扣含有线粒体,这就提出了一个问题,即没有线粒体的突触是否能够维持效能变化。为了解决这个问题,我们分析了出生后第15天(P15)和成年大鼠海马体中经过theta爆发刺激以产生长时程增强(TBS-LTP)的突触,并将它们与对照或无刺激的突触进行比较。在TBS-LTP后30分钟和120分钟,仅在P15时含有线粒体的突触前终扣中囊泡减少,并且在成年含有线粒体的终扣中囊泡减少最为明显。突触前线粒体嵴变宽,表明能量需求持续存在。因此,在增强达到稳定状态后很长时间,线粒体的接近程度反映了囊泡动员的增强,这与P15时新树突棘的明显沉默添加或成年时突触的沉默扩大并行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/e475036f1c37/elife-15275-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/030d72346844/elife-15275-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/58f62523f510/elife-15275-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/f0060e301799/elife-15275-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/77b9603c2b9b/elife-15275-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/691b76b56179/elife-15275-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/8b7112a40699/elife-15275-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/915a70af4ed9/elife-15275-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/eeaac1345287/elife-15275-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/147c5a1afe0b/elife-15275-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/e475036f1c37/elife-15275-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/030d72346844/elife-15275-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/58f62523f510/elife-15275-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/f0060e301799/elife-15275-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/77b9603c2b9b/elife-15275-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/691b76b56179/elife-15275-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/8b7112a40699/elife-15275-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/915a70af4ed9/elife-15275-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/eeaac1345287/elife-15275-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/147c5a1afe0b/elife-15275-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84f/5235352/e475036f1c37/elife-15275-fig10.jpg

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1
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2
A resource from 3D electron microscopy of hippocampal neuropil for user training and tool development.海马神经突 3D 电子显微镜资源,供用户培训和工具开发使用。
Sci Data. 2015 Sep 1;2:150046. doi: 10.1038/sdata.2015.46. eCollection 2015.
3
The role of mitochondrially derived ATP in synaptic vesicle recycling.线粒体源性ATP在突触小泡循环中的作用。
在长时程增强过程中,突触前囊泡为轴突终扣的增大提供膜。
bioRxiv. 2025 May 2:2025.04.29.651313. doi: 10.1101/2025.04.29.651313.
4
Fuelling synapses via lipid metabolism.通过脂质代谢为突触提供能量。
Nat Metab. 2025 Jul 1. doi: 10.1038/s42255-025-01306-w.
5
Volume electron microscopy reveals 3D synaptic nanoarchitecture in postmortem human prefrontal cortex.体积电子显微镜揭示了死后人类前额叶皮质中的三维突触纳米结构。
iScience. 2025 May 26;28(7):112747. doi: 10.1016/j.isci.2025.112747. eCollection 2025 Jul 18.
6
Regulation of synaptic mitochondria by extracellular vesicles and its implications for neuronal metabolism and synaptic plasticity.细胞外囊泡对突触线粒体的调控及其对神经元代谢和突触可塑性的影响。
J Cereb Blood Flow Metab. 2025 May 14:271678X251337630. doi: 10.1177/0271678X251337630.
7
Synaptic architecture of a memory engram in the mouse hippocampus.小鼠海马体中记忆印迹的突触结构。
Science. 2025 Mar 21;387(6740):eado8316. doi: 10.1126/science.ado8316.
8
Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy.三维电子显微镜揭示发育过程中神经肌肉系统线粒体的结构多样性
Adv Sci (Weinh). 2025 May;12(20):e2411191. doi: 10.1002/advs.202411191. Epub 2025 Mar 6.
9
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Curr Opin Neurobiol. 2025 Feb;90:102971. doi: 10.1016/j.conb.2025.102971. Epub 2025 Jan 24.
J Biol Chem. 2015 Sep 11;290(37):22325-36. doi: 10.1074/jbc.M115.656405. Epub 2015 Jun 30.
4
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PLoS One. 2015 Apr 30;10(4):e0125185. doi: 10.1371/journal.pone.0125185. eCollection 2015.
5
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Neuron. 2015 Apr 22;86(2):442-56. doi: 10.1016/j.neuron.2015.03.009. Epub 2015 Apr 2.
6
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10
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