<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(1)</volume><submitter>Menoret S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Regulatory T cells (Treg) in diverse species include CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells. In all species, CD8&lt;sup>+&lt;/sup> Treg have been only partially characterized and there is no rat model in which CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> FOXP3&lt;sup>+&lt;/sup> Treg are genetically tagged.&lt;h4>Results&lt;/h4>We generated a Foxp3-EGFP rat transgenic line in which FOXP3 gene was expressed and controlled EGFP. CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells were the only cells that expressed EGFP, in similar proportion as observed with anti-FOXP3 antibodies and co-labeled in the same cells. CD4&lt;sup>+&lt;/sup>EGFP&lt;sup>+&lt;/sup> Treg were 5-10 times more frequent than CD8&lt;sup>+&lt;/sup>EGFP&lt;sup>+&lt;/sup> Treg. The suppressive activity of CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> Treg was largely confined to EGFP&lt;sup>+&lt;/sup> cells. RNAseq analyses showed similarities but also differences among CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>+&lt;/sup> cells and provided the first description of the natural FOXP3&lt;sup>+&lt;/sup>CD8&lt;sup>+&lt;/sup> Treg transcriptome. In vitro culture of CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>-&lt;/sup> cells with TGFbeta and IL-2 generated induced EGFP&lt;sup>+&lt;/sup> Treg. CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>+&lt;/sup> Treg were expanded upon in vivo administration of a low dose of IL-2.&lt;h4>Conclusions&lt;/h4>This new and unique rat line constitutes a useful model to identify and isolate viable CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> FOXP3&lt;sup>+&lt;/sup> Treg. Additionally, it allows to identify molecules expressed in CD8&lt;sup>+&lt;/sup> Treg that may allow to better define their phenotype and function not only in rats but also in other species.</pubmed_abstract><journal>BMC biology</journal><pagination>8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9837914</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> regulatory T cell characterization in the rat using a unique transgenic Foxp3-EGFP model.</pubmed_title><pmcid>PMC9837914</pmcid><pubmed_authors>Gantier M</pubmed_authors><pubmed_authors>Menoret S</pubmed_authors><pubmed_authors>Tesson L</pubmed_authors><pubmed_authors>Usal C</pubmed_authors><pubmed_authors>Poschmann J</pubmed_authors><pubmed_authors>Anegon I</pubmed_authors><pubmed_authors>Guiffes A</pubmed_authors><pubmed_authors>Ouisse LH</pubmed_authors><pubmed_authors>Chenouard V</pubmed_authors><pubmed_authors>Gourain V</pubmed_authors><pubmed_authors>Fourgeux C</pubmed_authors><pubmed_authors>Heslan JM</pubmed_authors><pubmed_authors>Guillonneau C</pubmed_authors><pubmed_authors>Serazin C</pubmed_authors><pubmed_authors>Remy S</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> regulatory T cell characterization in the rat using a unique transgenic Foxp3-EGFP model.</name><description>&lt;h4>Background&lt;/h4>Regulatory T cells (Treg) in diverse species include CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells. In all species, CD8&lt;sup>+&lt;/sup> Treg have been only partially characterized and there is no rat model in which CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> FOXP3&lt;sup>+&lt;/sup> Treg are genetically tagged.&lt;h4>Results&lt;/h4>We generated a Foxp3-EGFP rat transgenic line in which FOXP3 gene was expressed and controlled EGFP. CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> T cells were the only cells that expressed EGFP, in similar proportion as observed with anti-FOXP3 antibodies and co-labeled in the same cells. CD4&lt;sup>+&lt;/sup>EGFP&lt;sup>+&lt;/sup> Treg were 5-10 times more frequent than CD8&lt;sup>+&lt;/sup>EGFP&lt;sup>+&lt;/sup> Treg. The suppressive activity of CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> Treg was largely confined to EGFP&lt;sup>+&lt;/sup> cells. RNAseq analyses showed similarities but also differences among CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>+&lt;/sup> cells and provided the first description of the natural FOXP3&lt;sup>+&lt;/sup>CD8&lt;sup>+&lt;/sup> Treg transcriptome. In vitro culture of CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>-&lt;/sup> cells with TGFbeta and IL-2 generated induced EGFP&lt;sup>+&lt;/sup> Treg. CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> EGFP&lt;sup>+&lt;/sup> Treg were expanded upon in vivo administration of a low dose of IL-2.&lt;h4>Conclusions&lt;/h4>This new and unique rat line constitutes a useful model to identify and isolate viable CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> FOXP3&lt;sup>+&lt;/sup> Treg. Additionally, it allows to identify molecules expressed in CD8&lt;sup>+&lt;/sup> Treg that may allow to better define their phenotype and function not only in rats but also in other species.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-06-21T03:21:39.089Z</modification><creation>2025-05-29T16:22:48.273Z</creation></dates><accession>S-EPMC9837914</accession><cross_references><pubmed>36635667</pubmed><doi>10.1186/s12915-022-01502-0</doi></cross_references></HashMap>