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基于共表达网络分析的衰老小鼠大脑驱动变化的蛋白质组学特征。

Proteomic characterization of aging-driven changes in the mouse brain by co-expression network analysis.

机构信息

Center for Integrated Medical Research, Keio University School of Medicine, Shinjuku-ku, Tokyo, 160-8582, Japan.

Proteome Homeostasis Research Unit, RIKEN Center for Integrative Medical Sciences, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.

出版信息

Sci Rep. 2023 Oct 24;13(1):18191. doi: 10.1038/s41598-023-45570-w.

DOI:10.1038/s41598-023-45570-w
PMID:37875604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10598061/
Abstract

Brain aging causes a progressive decline in functional capacity and is a strong risk factor for dementias such as Alzheimer's disease. To characterize age-related proteomic changes in the brain, we used quantitative proteomics to examine brain tissues, cortex and hippocampus, of mice at three age points (3, 15, and 24 months old), and quantified more than 7000 proteins in total with high reproducibility. We found that many of the proteins upregulated with age were extracellular proteins, such as extracellular matrix proteins and secreted proteins, associated with glial cells. On the other hand, many of the significantly downregulated proteins were associated with synapses, particularly postsynaptic density, specifically in the cortex but not in the hippocampus. Our datasets will be helpful as resources for understanding the molecular basis of brain aging.

摘要

大脑衰老导致功能能力逐渐下降,是阿尔茨海默病等痴呆症的一个重要危险因素。为了描述大脑中与年龄相关的蛋白质组变化,我们使用定量蛋白质组学方法检测了三个年龄点(3、15 和 24 个月)的小鼠脑组织、皮层和海马组织,总共定量了超过 7000 种具有高重复性的蛋白质。我们发现,许多随年龄上调的蛋白质是细胞外蛋白质,如细胞外基质蛋白和分泌蛋白,与神经胶质细胞有关。另一方面,许多显著下调的蛋白质与突触有关,特别是突触后密度,特别是在皮层而不是海马体中。我们的数据集将有助于理解大脑衰老的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/d040441f885d/41598_2023_45570_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/04291fac59b7/41598_2023_45570_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/f92261cbe8ca/41598_2023_45570_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/d040441f885d/41598_2023_45570_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/04291fac59b7/41598_2023_45570_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/f92261cbe8ca/41598_2023_45570_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8470/10598061/d040441f885d/41598_2023_45570_Fig3_HTML.jpg

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iScience. 2022 Aug 5;25(8):104832. doi: 10.1016/j.isci.2022.104832. eCollection 2022 Aug 19.
2
Neuroinflammation in neurodegenerative disorders: the roles of microglia and astrocytes.神经退行性疾病中的神经炎症:小胶质细胞和星形胶质细胞的作用。
Transl Neurodegener. 2020 Nov 26;9(1):42. doi: 10.1186/s40035-020-00221-2.
3
Isobaric Matching between Runs and Novel PSM-Level Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification.
衰老的黑质以活性氧积累为特征,这可能导致神经炎症增加和细胞骨架重塑。
Adv Biol (Weinh). 2025 Apr;9(4):e2400814. doi: 10.1002/adbi.202400814. Epub 2025 Mar 12.
4
Mechanisms of astrocyte aging in reactivity and disease.反应性和疾病中星形胶质细胞衰老的机制。
Mol Neurodegener. 2025 Feb 21;20(1):21. doi: 10.1186/s13024-025-00810-7.
5
Expanding the Landscape of Aging via Orbitrap Astral Mass Spectrometry and Tandem Mass Tag (TMT) Integration.通过轨道阱星质谱法和串联质谱标签(TMT)整合拓展衰老研究领域
bioRxiv. 2024 Dec 17:2024.12.13.628374. doi: 10.1101/2024.12.13.628374.
6
Aging disrupts blood-brain and blood-spinal cord barrier homeostasis, but does not increase paracellular permeability.衰老会破坏血脑屏障和血脊髓屏障的稳态,但不会增加细胞旁通透性。
Geroscience. 2025 Feb;47(1):263-285. doi: 10.1007/s11357-024-01404-9. Epub 2024 Oct 30.
运行间等压匹配和 MaxQuant 中全新的 PSM 水平归一化方法显著提高基于报告离子的定量分析。
J Proteome Res. 2020 Oct 2;19(10):3945-3954. doi: 10.1021/acs.jproteome.0c00209. Epub 2020 Sep 16.
4
Sample multiplexing for targeted pathway proteomics in aging mice.靶向通路蛋白质组学在衰老小鼠中的样品多重分析。
Proc Natl Acad Sci U S A. 2020 May 5;117(18):9723-9732. doi: 10.1073/pnas.1919410117. Epub 2020 Apr 24.
5
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Nat Med. 2020 May;26(5):769-780. doi: 10.1038/s41591-020-0815-6. Epub 2020 Apr 13.
6
Type I interferon response drives neuroinflammation and synapse loss in Alzheimer disease.I 型干扰素反应导致阿尔茨海默病中的神经炎症和突触丧失。
J Clin Invest. 2020 Apr 1;130(4):1912-1930. doi: 10.1172/JCI133737.
7
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Tissue Barriers. 2019;7(4):1651157. doi: 10.1080/21688370.2019.1651157. Epub 2019 Sep 11.
8
Ageing as a risk factor for neurodegenerative disease.衰老作为神经退行性疾病的一个风险因素。
Nat Rev Neurol. 2019 Oct;15(10):565-581. doi: 10.1038/s41582-019-0244-7. Epub 2019 Sep 9.
9
Basement membrane and blood-brain barrier.基底膜和血脑屏障。
Stroke Vasc Neurol. 2018 Dec 5;4(2):78-82. doi: 10.1136/svn-2018-000198. eCollection 2019 Jul.
10
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