<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Oosterlynck M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Alzheimer's disease (AD) is the most prominent form of dementia worldwide. It is characterized by tau lesions that spread throughout the brain in a spatio-temporal manner. This has led to the prion-like propagation hypothesis implicating a transfer of pathological tau seeds from cell to cell. Human brain-derived extracellular vesicles (BD-EVs) isolated from the brain-derived fluid of AD patients contain seeds that contribute to this tau pathology spreading. Knowing the rich diversity of EVs, isolation of functional EV sub-populations is required to unravel their implication in the pathophysiology of AD.&lt;h4>Methods&lt;/h4>Here, enriched-small EVs (eSEVs) and enriched-large EVs (eLEVs) were isolated from frozen tissues after collagenase enzymatic brain dissociation to guarant</pubmed_abstract><journal>Translational neurodegeneration</journal><pagination>63</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12679798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Stratification of brain-derived extracellular vesicles of Alzheimer's disease patients indicates a unique proteomic content and a higher seeding capacity of small extracellular vesicles.</pubmed_title><pmcid>PMC12679798</pmcid><pubmed_authors>Buee L</pubmed_authors><pubmed_authors>Bouillet T</pubmed_authors><pubmed_authors>Maurage CA</pubmed_authors><pubmed_authors>Lefebvre C</pubmed_authors><pubmed_authors>Caillierez R</pubmed_authors><pubmed_authors>Leroux E</pubmed_authors><pubmed_authors>Mazur D</pubmed_authors><pubmed_authors>Accart B</pubmed_authors><pubmed_authors>Perbet R</pubmed_authors><pubmed_authors>Aboulouard S</pubmed_authors><pubmed_authors>Namasivayam B</pubmed_authors><pubmed_authors>Colin M</pubmed_authors><pubmed_authors>Oosterlynck M</pubmed_authors><pubmed_authors>Loyens A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stratification of brain-derived extracellular vesicles of Alzheimer's disease patients indicates a unique proteomic content and a higher seeding capacity of small extracellular vesicles.</name><description>&lt;h4>Background&lt;/h4>Alzheimer's disease (AD) is the most prominent form of dementia worldwide. It is characterized by tau lesions that spread throughout the brain in a spatio-temporal manner. This has led to the prion-like propagation hypothesis implicating a transfer of pathological tau seeds from cell to cell. Human brain-derived extracellular vesicles (BD-EVs) isolated from the brain-derived fluid of AD patients contain seeds that contribute to this tau pathology spreading. Knowing the rich diversity of EVs, isolation of functional EV sub-populations is required to unravel their implication in the pathophysiology of AD.&lt;h4>Methods&lt;/h4>Here, enriched-small EVs (eSEVs) and enriched-large EVs (eLEVs) were isolated from frozen tissues after collagenase enzymatic brain dissociation to guarant</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-07-15T07:46:28.586Z</modification><creation>2026-07-01T03:07:50.394Z</creation></dates><accession>S-EPMC12679798</accession><cross_references><pubmed>41345709</pubmed><doi>10.1186/s40035-025-00519-z</doi></cross_references></HashMap>