<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Soh WC</submitter><funding>National Research Foundation of Korea (NRF)</funding><funding>National Cancer Center</funding><funding>National Cancer Center (NCC)</funding><funding>National Research Foundation of Korea</funding><pagination>e2505291122</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12318239</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>122(30)</volume><pubmed_abstract>Microvilli on T cells differ from those on epithelial cells, exhibiting filopodia-like characteristics that facilitate the clustering of molecules essential for sensing and cell migration. Recently, they have also been recognized as the structures from which T cell immunological synaptosomes (TIS) are released. In this study, we examined a key determinant of microvilli organization during T cell development and explored the functional roles of these structures, particularly in relation to T cell behaviors. During thymocyte maturation, single-positive thymocytes were found to develop more and longer microvilli than double-positive thymocytes. However, the deletion or inhibition of Cdc42, a small Rho family protein, significantly reduced both the number and length of microvilli in single-pos</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pubmed_title>&amp;lt;i&amp;gt;Cdc42&amp;lt;/i&amp;gt; defect reveals insights into microvilli organization and function in T cell immunity.</pubmed_title><pmcid>PMC12318239</pmcid><funding_grant_id>RS-2024-00419699</funding_grant_id><funding_grant_id>RS-2024-0034-0032</funding_grant_id><funding_grant_id>RS-2024-00341869</funding_grant_id><funding_grant_id>2022R1A2C4002627</funding_grant_id><funding_grant_id>NCC-2310600-3</funding_grant_id><funding_grant_id>2015R1A3A2066253</funding_grant_id><pubmed_authors>Park SM</pubmed_authors><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Kim MS</pubmed_authors><pubmed_authors>Park J</pubmed_authors><pubmed_authors>Jun CD</pubmed_authors><pubmed_authors>Karabulut H</pubmed_authors><pubmed_authors>Kang HT</pubmed_authors><pubmed_authors>Soh WC</pubmed_authors><pubmed_authors>Kim HR</pubmed_authors><pubmed_authors>Park JS</pubmed_authors><pubmed_authors>Kang SK</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;Cdc42&amp;lt;/i&amp;gt; defect reveals insights into microvilli organization and function in T cell immunity.</name><description>Microvilli on T cells differ from those on epithelial cells, exhibiting filopodia-like characteristics that facilitate the clustering of molecules essential for sensing and cell migration. Recently, they have also been recognized as the structures from which T cell immunological synaptosomes (TIS) are released. In this study, we examined a key determinant of microvilli organization during T cell development and explored the functional roles of these structures, particularly in relation to T cell behaviors. During thymocyte maturation, single-positive thymocytes were found to develop more and longer microvilli than double-positive thymocytes. However, the deletion or inhibition of Cdc42, a small Rho family protein, significantly reduced both the number and length of microvilli in single-pos</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-06-02T10:04:23.442Z</modification><creation>2025-08-12T03:04:28.439Z</creation></dates><accession>S-EPMC12318239</accession><cross_references><pubmed>40711916</pubmed><doi>10.1073/pnas.2505291122</doi></cross_references></HashMap>