Kaplelach Azariah K, Murchison Charles F, Kojima Kyoko, Mobley James A, Arrant Andrew E
Center for Neurodegeneration and Experimental Therapeutics, Alzheimer's Disease Center, Evelyn F. McKnight Brain Institute, Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Institutional Research Core Program/Mass Spectrometry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Aging Cell. 2025 Jan;24(1):e14359. doi: 10.1111/acel.14359. Epub 2024 Oct 8.
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.
细胞外囊泡(EVs)由大脑的所有主要细胞类型分泌,提供了一种细胞间通讯方式和细胞碎片处理途径。EVs有助于维持大脑的健康功能,但也可能导致影响大脑的疾病。EVs可能与大脑衰老有关,因为炎症和细胞衰老等与衰老相关的过程可能会改变EV的货物成分,促进进一步的炎症和衰老。然而,衰老对大脑EVs的影响以及EVs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小鼠大脑中分离出的EVs的水平和蛋白质货物。我们检测到EV水平没有变化,但观察到EV蛋白质存在年龄依赖性变化。老年(22个月大)大脑的EV组分比年轻(4个月大)大脑的EV组分含有更高水平的细胞外基质蛋白,12个月大大脑的EV组分则处于中间水平。具体而言,老年小鼠的EV组分中透明质酸和蛋白聚糖连接蛋白1和2以及几种硫酸软骨素蛋白聚糖(CSPGs)的水平升高。对老年小鼠几个脑区的细胞外基质分析显示,CSPG聚集蛋白聚糖的免疫标记增加,但与紫藤凝集素的标记减少,紫藤凝集素可与CSPGs的硫酸软骨素侧链结合。这些数据与先前显示老年大脑细胞外基质组成变化的研究一致,并表明EVs与衰老大脑细胞外基质变化之间存在新的关联。