<<< Full experiment listing

PXD041789

PXD041789 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleProteomic quantification of native and ECM-enriched mouse ovaries reveals an age-dependent fibro-inflammatory signature
DescriptionThe 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.
HostingRepositoryMassIVE
AnnounceDate2023-12-18
AnnouncementXMLSubmission_2023-12-18_15:02:25.905.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterChristina King
SpeciesList scientific name: Mus musculus; common name: house mouse; NCBI TaxID: 10090;
ModificationListNo PTMs are included in the dataset
InstrumentOrbitrap Exploris 480
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-04-24 14:57:28ID requested
12023-12-18 15:02:26announced
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 affiliationBuck Institute
contact emailbschilling@buckinstitute.org
lab head
Christina King
contact affiliationBuck Institute for Research on Aging
contact emailcking@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/