<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu L</submitter><funding>National Natural Science Foundation of China</funding><pagination>519</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9733225</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Proliferative vitreoretinopathy (PVR) is a blind-causing disease initiated by the activation of retinal pigmented epithelium (RPE) primarily induced by TGF-β families. Migrasome is a recently discovered type of extracellular vesicle related to cell migration.&lt;h4>Results&lt;/h4>Here, we used ex vivo, in vitro, and in vivo models, to investigate the characteristics and functions of migrasomes in RPE activation and PVR development. Results indicated that the migrasome marker tetraspanin-4 (TSPAN4) was abundantly expressed in human PVR-associated clinical samples. The ex vivo model PVR microenvironment is simulated by incubating brown Norway rat RPE eyecups with TGF-β1. Electron microscope images showed the formation of migrasome-like vesicles during the activation of RPE. Furt</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>TSPAN4-positive migrasome derived from retinal pigmented epithelium cells contributes to the development of proliferative vitreoretinopathy.</pubmed_title><pmcid>PMC9733225</pmcid><funding_grant_id>81770939</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Feng L</pubmed_authors><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Gu X</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Xu G</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>TSPAN4-positive migrasome derived from retinal pigmented epithelium cells contributes to the development of proliferative vitreoretinopathy.</name><description>&lt;h4>Background&lt;/h4>Proliferative vitreoretinopathy (PVR) is a blind-causing disease initiated by the activation of retinal pigmented epithelium (RPE) primarily induced by TGF-β families. Migrasome is a recently discovered type of extracellular vesicle related to cell migration.&lt;h4>Results&lt;/h4>Here, we used ex vivo, in vitro, and in vivo models, to investigate the characteristics and functions of migrasomes in RPE activation and PVR development. Results indicated that the migrasome marker tetraspanin-4 (TSPAN4) was abundantly expressed in human PVR-associated clinical samples. The ex vivo model PVR microenvironment is simulated by incubating brown Norway rat RPE eyecups with TGF-β1. Electron microscope images showed the formation of migrasome-like vesicles during the activation of RPE. Furt</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T19:19:10.259Z</modification><creation>2024-11-12T23:05:58.752Z</creation></dates><accession>S-EPMC9733225</accession><cross_references><pubmed>36494806</pubmed><doi>10.1186/s12951-022-01732-y</doi></cross_references></HashMap>