<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>111(23)</volume><submitter>Tamzalit F</submitter><pubmed_abstract>Interleukin (IL)-15 and its specific receptor chain, IL-15Rα, support the development of various effector cells, including NK and CD8 T cells via a mechanism called trans-presentation. Whereas the dynamic of trans-presentation has been shown to involve the recycling of IL-15Rα by presenting cells, the way responding cells integrate, or take advantage of this process has not been evaluated yet. To address this question, we set up a trans-presentation model using a membrane-bound IL-15.IL-15Rα fusion protein, and found that IL-15 is detectable within responding cells following IL-15 trans-presentation. The role of the proteolytic cleavage of IL-15Rα in this process was investigated by generating an uncleavable form of IL-15Rα. We showed that IL-15 entry into responding cells necessitates the</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>8565-70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4060713</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>IL-15.IL-15Rα complex shedding following trans-presentation is essential for the survival of IL-15 responding NK and T cells.</pubmed_title><pmcid>PMC4060713</pmcid><pubmed_authors>Mortier E</pubmed_authors><pubmed_authors>Jacques Y</pubmed_authors><pubmed_authors>Heim J</pubmed_authors><pubmed_authors>Plet A</pubmed_authors><pubmed_authors>Tamzalit F</pubmed_authors><pubmed_authors>Nedellec S</pubmed_authors><pubmed_authors>Morisseau S</pubmed_authors><pubmed_authors>Barbieux I</pubmed_authors></additional><is_claimable>false</is_claimable><name>IL-15.IL-15Rα complex shedding following trans-presentation is essential for the survival of IL-15 responding NK and T cells.</name><description>Interleukin (IL)-15 and its specific receptor chain, IL-15Rα, support the development of various effector cells, including NK and CD8 T cells via a mechanism called trans-presentation. Whereas the dynamic of trans-presentation has been shown to involve the recycling of IL-15Rα by presenting cells, the way responding cells integrate, or take advantage of this process has not been evaluated yet. To address this question, we set up a trans-presentation model using a membrane-bound IL-15.IL-15Rα fusion protein, and found that IL-15 is detectable within responding cells following IL-15 trans-presentation. The role of the proteolytic cleavage of IL-15Rα in this process was investigated by generating an uncleavable form of IL-15Rα. We showed that IL-15 entry into responding cells necessitates the</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jun</publication><modification>2025-04-05T13:37:30.805Z</modification><creation>2019-03-27T01:30:21Z</creation></dates><accession>S-EPMC4060713</accession><cross_references><pubmed>24912180</pubmed><doi>10.1073/pnas.1405514111</doi></cross_references></HashMap>