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PXD070221

PXD070221 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleProteomic validation of MEG-01-Derived Extracellular Vesicles as Biologically Representative Models for Megakaryocyte- and Platelet-Derived Extracellular Vesicles.
DescriptionPlatelets and their extracellular vesicles (EVs) have emerged as promising liquid biopsy biosources for cancer detection and monitoring. The megakaryoblastic MEG-01 cell line offers a controlled system for generating platelet-like particles (PLPs) and EVs through valproic acid induced differentiation. Here, we performed comprehensive characterization and proteomic validation of MEG-01-derived populations, native human platelets and their EVs using nanoparticle tracking analysis, transmission electron microscopy, imaging flow cytometry and quantitative proteomics. MEG-01 megakaryocytic differentiation is characterized by polylobulated nuclei, proplatelet formation and elevated CD41/CD42a expression. PLPs predominantly exhibit an activated-like phenotype (CD62P+, degranulated morphology), while microvesicles (100-500 nm) and exosomes (50-250 nm) displayed size distributions and phenotypic markers consistent with native platelet-derived EVs. Proteomics identified substantial core proteomes shared across fractions and fraction-specific patterns consistent with selective cargo partitioning during EV biogenesis. Functional enrichment revealed that MEG-01-derived vesicles retained hemostatic, cytoskeletal and immune pathways characteristic of physiological platelet EVs. Ingenuity Pathway Analysis demonstrated that PLPs maintained proliferative transcriptional programs (elevated MYC/RB1/TEAD1, reduced GATA1), while plasma exosomes showed minimal differential pathway activation relative to MEG-01 exosomes. These findings validate MEG-01-derived EVs as representative of megakaryocyte-lineage exosomes and activated platelet-like states; plasma exosomes converge proteomically with EXOs MEG-01, whereas platelet exosomes retain distinct activation-associated features.
HostingRepositoryPRIDE
AnnounceDate2026-01-05
AnnouncementXMLSubmission_2026-01-05_00:27:45.291.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterCarolina Torres Perales
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606;
ModificationListNo PTMs are included in the dataset
InstrumenttimsTOF
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-11-03 02:51:16ID requested
12026-01-05 00:27:46announced
Publication List
Sanchez-Manas JM, Perales S, Martinez-Navajas G, Ceron-Hernandez J, Lopez CM, Peralbo-Molina A, Delgado JR, Martinez-Galan J, Ramos-Mejia V, Chicano-Galvez E, Hernandez-Valladares M, Ortuno FM, Torres C, Real PJ, Proteomic Validation of MEG-01-Derived Extracellular Vesicles as Representative Models for Megakaryocyte- and Platelet-Derived Extracellular Vesicles. Biomolecules, 15(12):(2025) [pubmed]
10.3390/biom15121698;
Keyword List
submitter keyword: MEG-01 cell line, Exosomes (EXOs)., Extracellular Vesicles (EVs), Proteomics, Microvesicles (MVs), Platelets
Contact List
Pedro J. Real
contact affiliation1. Gene Regulation, Stem Cells and Development group, PTS, Granada GENyO, Pfizer-University of Granada-Andalusian Regional Government Centre for Genomics and Oncological Research, Avenida de la Ilustración 114, 18016 Granada, Spain. 2. Department of Biochemistry and Molecular Biology I, Faculty of Science, University of Granada, Avenida Fuentenueva s/n, 18071 Granada, Spain. 3. Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
contact emailpedro.real@genyo.es
lab head
Carolina Torres Perales
contact affiliationDepartment of Biochemistry and Molecular Biology III and Immunology, University of Granada
contact emailctp@ugr.es
dataset submitter
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