PXD052797 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Increased levels of extracellular matrix proteins in extracellular vesicles from brains of aged mice. |
Description | Extracellular vesicles (EVs) have several functions in the brain, serving as a mode of intercellular communication and as a pathway for disposal of cellular debris. While these functions serve to maintain healthy brain function, they may also contribute to diseases affecting the brain. EVs also change with aging of the brain, as levels of some EV subtypes increase at advanced ages in mice. These changes could be caused by aging-related changes such as inflammation, cellular senescence, or impairment of autophagy or mitochondrial function. Aging-related changes in brain EVs might also further aging-related changes, as levels of EVs in plasma may change with age and contribute to aging-related changes in inflammation and cellular metabolism. However, the effects of aging on brain EVs and the potential contribution of EVs to aging-related changes in the brain are not well understood. To address this question, we investigated the levels and protein contents of EVs isolated from 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) mice contained higher levels of extracellular matrix proteins than EV fractions from young (4-month–old) mice, with similar trends occurring in 12-month–old mice. Specifically, levels of hyaluronan and proteoglycan link proteins (Hapln) 1 and 2 were elevated in EV fractions from aged mice, as were levels of several chondroitin sulfate proteoglycans (CSPGs), which interact with Hapln1 and 2. Analysis of extracellular matrix in several brain regions of aged mice revealed increased immunolabeling for aggrecan, but an overall reduction in labeling with Wisteria floribunda agglutinin, which binds to chondroitin sulfate. These data are consistent with prior studies showing changes to the composition of extracellular matrix in aged brains, which might contribute to age-related cognitive decline. These findings reveal a novel association of EVs with changes in the extracellular matrix of the aging brain. |
HostingRepository | PRIDE |
AnnounceDate | 2025-05-07 |
AnnouncementXML | Submission_2025-05-06_18:11:45.391.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD052797 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | james mobley |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | No PTMs are included in the dataset |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-06-03 10:56:50 | ID requested | |
⏵ 1 | 2025-05-06 18:11:46 | announced | |
Publication List
Kaplelach AK, Murchison CF, Kojima K, Mobley JA, Arrant AE, Increased levels of extracellular matrix proteins associated with extracellular vesicles from brains of aged mice. Aging Cell, 24(1):e14359(2025) [pubmed] |
10.6019/PXD052797; |
10.1111/acel.14359; |
Keyword List
submitter keyword: Aging,Extracellular vesicles, Extracellular matrix, LCMS, Mouse Model, Proteomics |
Contact List
James Mobley, Ph.D. |
contact affiliation | University of Alabama at Birmingham, IRCP Heersink & CCC O'Neal Proteomics Shared Resource Facility |
contact email | mobleyja@uab.edu |
lab head | |
james mobley |
contact affiliation | University of Alabama at Birmingham |
contact email | mobleyja@uab.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD052797
- Label: PRIDE project
- Name: Increased levels of extracellular matrix proteins in extracellular vesicles from brains of aged mice.