PXD041789
PXD041789 is an original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proteomic quantification of native and ECM-enriched mouse ovaries reveals an age-dependent fibro-inflammatory signature |
Description | The ovarian microenvironment becomes fibrotic and stiff with age due in part to increased stromal collagen and decreased hyaluronan. However, the extracellular matrix (ECM) is a complex network of hundreds of proteins, glycoproteins and glycans which are highly tissue specific and undergo pronounced changes with age. We used a label-free quantitative proteomic methodology to obtain an unbiased and comprehensive protein profile of age-associated alterations of the mammalian ovarian proteome. We analyzed ovaries from reproductively young and old mice using both native and ECM-enriched tissues to specifically interrogate the extracellular matrix. We optimized and validated conditions to enrich for the ECM prior to proteomic analysis and determined that treatment of ovaries with 0.1% SDS for 12.5 hours efficiently removed nuclear material, while maintaining the integrity of the ECM. Following the analysis by data-independent acquisition (DIA), both native and ECM-enriched samples clustered separately based on age, indicating that ovaries from reproductively young and old mice feature clearly distinct proteomic signatures. We identified a total of 4,721 proteins and 383 proteins that are significantly-altered with advanced reproductive age, including key ECM proteins. In addition to ECM proteins, immunoglobulins, proteins that regulate metal homeostasis, and tumor suppressors were highly upregulated with age, whereas downregulated proteins were consistent with the age-dependent decline in fertility. Pathways regulating genomic instability and proteostasis were downregulated with age. Biological processes associated with immune function and ECM remodeling were upregulated with age. These findings provide evidence from a proteomic perspective that the aging ovary provides a fibroinflammatory milieu, and our study suggests target proteins which may drive these age-associated phenotypes for future investigation. |
HostingRepository | MassIVE |
AnnounceDate | 2023-12-18 |
AnnouncementXML | Submission_2023-12-18_15:02:25.905.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Christina King |
SpeciesList | scientific name: Mus musculus; common name: house mouse; NCBI TaxID: 10090; |
ModificationList | No PTMs are included in the dataset |
Instrument | Orbitrap Exploris 480 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
---|---|---|---|
0 | 2023-04-24 14:57:28 | ID requested | |
⏵ 1 | 2023-12-18 15:02:26 | announced |
Publication List
Dipali SS, King CD, Rose JP, Burdette JE, Campisi J, Schilling B, Duncan FE, Proteomic quantification of native and ECM-enriched mouse ovaries reveals an age-dependent fibro-inflammatory signature. Aging (Albany NY), 15(20):10821-10855(2023) [pubmed] |
Keyword List
submitter keyword: reproductive aging, ovary, proteomics, extracellular matrix, matrisome, data-independent acquisition |
Contact List
Birgit Schilling | |
---|---|
contact affiliation | Buck Institute |
contact email | bschilling@buckinstitute.org |
lab head | |
Christina King | |
contact affiliation | Buck Institute for Research on Aging |
contact email | cking@buckinstitute.org |
dataset submitter |
Full Dataset Link List
MassIVE dataset URI |
Dataset FTP location NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://massive.ucsd.edu/MSV000091790/ |