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PXD062092-1

PXD062092 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleProteomic signatures of retinal pigment epithelium-derived exosomes in myopic and non-myopic tree shrew eyes
DescriptionPurpose: The retinal pigment epithelium (RPE) transmits growth signals from the neural retina to the choroid in the emmetropization pathway, but the underlying molecular mechanisms remain poorly understood. Here, we compared the proteomic profiles of RPE-derived exosomes between myopic and non-myopic eyes of tree shrews, dichromatic mammals closely related to primates. Methods: Four myopic (159–210 days of visual experience, DVE) and seven non-myopic eyes (156–210 DVE) of tree shrews were included. Non-cycloplegic refractive error was measured with Nidek autorefractor, and axial ocular component dimensions were recorded with LenStar. Tissue was collected, yielding RPE-lined eyecups, which were subsequently incubated in L-15 culture media for two hours. The RPE-derived exosomes were then enriched and purified from the incubation media by double ultracentrifugation and characterized by imaging and molecular methods. Exosomal proteins were identified and quantified with mass spectrometry, analyzed using Gene Ontology (GO), and compared between myopic and non-myopic samples. Results: Out of 506 RPE exosomal proteins identified, 48 and 41 were unique to the myopic and non-myopic samples, respectively. There were 286 differentially expressed proteins in the myopic samples, including 79 upregulated and 70 downregulated. The top three upregulated proteins were Histone H4 (FC=3.04, p=0.09), PTB 1 (FC=2.59, p=0.08) and Histone H3.1 (FC=2.59, p=0.13), while the top three downregulated proteins were RPS5 (FC=-2.41, p=0.004), ACOT7 (FC=-2.15, p=0.04) and CRYBB2 (FC=-2.14, p=0.05). Other differentially expressed proteins included LUM, VCL, SEPTIN11, GPX3, SPTBN1, SEPTIN7, RPL10A, KCTD12, FGG, and FMOD. Proteomic analysis revealed a low abundance of ATP6V1B2, crystallin beta B2, and Arrestin-C proteins, and a significant depletion of the crystallin protein family (crystallin A2, A3, and B3 subunits) in the myopic samples. The GO and functional analyses showed extracellular matrix, cytoskeletal dynamic, and cell-matrix adhesion as the primary components associated with the RPE exosomal proteins in myopic eyes. Conclusion: Using standard molecular and imaging techniques, this study provides the first demonstration of the ex-vivo RPE exosome biogenesis from tree shrew eyes. The results showed distinct differential expressions of the RPE exosomal proteins between the myopic and non-myopic eyes, with several proteins unique to each group. Future targeted proteomic studies of identified candidate exosomal protein signatures could elucidate the molecular mechanism of RPE exosome-mediated growth signal transmission in the emmetropization pathway.
HostingRepositoryPRIDE
AnnounceDate2026-08-31
AnnouncementXMLSubmission_2026-08-30_16:11:35.937.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterjames mobley
SpeciesList scientific name: Tupaia; NCBI TaxID: NEWT:9394;
ModificationListNo PTMs are included in the dataset
InstrumentQ Exactive HF
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-03-20 16:56:00ID requested
12026-08-30 16:11:36announced
Publication List
Sanchez NC, Roig-Lopez JL, Mobley JA, Khanal S, Proteomic signatures of retinal pigment epithelium-derived exosomes in myopic and non-myopic tree shrew eyes. Front Med (Lausanne), 12():1523211(2025) [pubmed]
10.3389/fmed.2025.1523211;
Keyword List
submitter keyword: exosomes, tree shrews, proteomics,myopia, retinal pigment epithelium, emmetropization
Contact List
James Mobley
contact affiliationDirector UAB Proteomics Facility
contact emailmobleyja@uab.edu
lab head
james mobley
contact affiliationUniversity of Alabama at Birmingham
contact emailmobleyja@uab.edu
dataset submitter
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