老龄小鼠大脑中与细胞外囊泡相关的细胞外基质蛋白含量增加。

IF 8 1区 医学 Q1 CELL BIOLOGY Aging Cell Pub Date : 2024-10-08 DOI:10.1111/acel.14359
Azariah K Kaplelach, Charles F Murchison, Kyoko Kojima, James A Mobley, Andrew E Arrant
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引用次数: 0

摘要

细胞外囊泡(EVs)是大脑所有主要细胞类型分泌的物质,它提供了一种细胞间交流的模式和处理细胞碎片的途径。EVs 有助于维持健康的大脑功能,但也可能导致影响大脑的疾病。EVs 可能会导致大脑衰老,因为与衰老相关的过程(如炎症和细胞衰老)可能会改变 EV 货物,进一步促进炎症和衰老。然而,人们对衰老对大脑 EV 的影响以及 EV 在衰老大脑中的功能仍知之甚少。为了解决这个问题,我们测量了从 4 个月、12 个月和 22 个月大的 C57BL/6J 小鼠大脑中分离出来的 EVs 的水平和蛋白载体。我们检测到EV水平没有变化,但观察到EV蛋白随年龄而变化。老年(22 个月大)小鼠大脑中的 EV 组份含有的细胞外基质蛋白水平高于年轻(4 个月大)小鼠大脑中的 EV 组份,而 12 个月大(22 个月大)小鼠大脑中的 EV 组份含有的细胞外基质蛋白水平介于两者之间。具体来说,老年小鼠的EV馏分中透明质酸、蛋白多糖连接蛋白1和2以及几种硫酸软骨素蛋白多糖(CSPGs)的含量较高。对老龄小鼠多个脑区细胞外基质的分析表明,CSPG aggrecan 的免疫标记增加了,但与 CSPG 硫酸软骨素侧链结合的紫藤凝集素的标记却减少了。这些数据与之前显示衰老大脑细胞外基质成分变化的研究一致,并表明了 EVs 与衰老大脑细胞外基质变化之间的新关联。
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Increased levels of extracellular matrix proteins associated with extracellular vesicles from brains of aged mice.

Extracellular vesicles (EVs) are secreted by all major cell types of the brain, providing a mode of intercellular communication and a pathway for disposal of cellular debris. EVs help maintain healthy brain function, but may also contribute to diseases affecting the brain. EVs might contribute to aging of the brain, as aging-related processes such as inflammation and cellular senescence may alter EV cargo, promoting further inflammation and senescence. However, the effects of aging on brain EVs and the function of EVs in the aging brain remain poorly understood. To address this question, we measured the levels and protein cargo of EVs isolated from the brains of 4-, 12-, and 22-month-old C57BL/6J mice. We detected no changes in EV levels, but observed age-dependent changes in EV proteins. EV fractions from aged (22 month old) brains contained higher levels of extracellular matrix proteins than EV fractions from young (4 month old) brains, with intermediate levels in 12-month-old brains. Specifically, EV fractions from aged mice contained elevated levels of hyaluronan and proteoglycan link proteins 1 and 2 and several chondroitin sulfate proteoglycans (CSPGs). Analysis of extracellular matrix in several brain regions of aged mice revealed increased immunolabeling for the CSPG aggrecan, but reduced labeling with Wisteria floribunda agglutinin, which binds to chondroitin sulfate side chains of CSPGs. These data are consistent with prior studies showing changes to the composition of extracellular matrix in aged brains, and indicate a novel association of EVs with changes in the extracellular matrix of the aging brain.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
期刊最新文献
Contextualizing aging clocks and properly describing biological age. CaMKIIα-TARPγ8 signaling mediates hippocampal synaptic impairment in aging. Correction to "An interpretable machine learning-based cerebrospinal fluid proteomics clock for predicting age reveals novel insights into brain aging". Hippocampal rejuvenation by a single intracerebral injection of one-carbon metabolites in C57BL6 old wild-type mice. Increased levels of extracellular matrix proteins associated with extracellular vesicles from brains of aged mice.
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