<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hersh J</submitter><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>Cancer Prevention and Research Institute of Texas</funding><pagination>577455</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7856103</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>351</volume><pubmed_abstract>We determined that T-cell astrocyte interaction modulates interleukin-10 (IL-10) production from both cell types. The impact of IL-10 on astrocytes was compared to IL-10 generated from T-cell-astrocyte interactions in vitro. We demonstrated that T-cells directly interact with astrocytes to upregulate gene expression and secretion of IL-10, confirmed by elevated STAT3p/STAT3 expression in astrocytes. IL-10 increased astrocytes proliferation. In addition, IL-10 treatment and CD4+ co-culture shifts primary astrocytes toward a more energetic phenotype. These findings indicate that direct interaction of CD4+ T-cells with astrocytes, activated the IL-10 anti-inflammatory pathway, altering astrocyte phenotype, metabolism, and proliferation.</pubmed_abstract><journal>Journal of neuroimmunology</journal><pubmed_title>Modulation of astrocyte phenotype in response to T-cell interaction.</pubmed_title><pmcid>PMC7856103</pmcid><funding_grant_id>T32 AG020494</funding_grant_id><funding_grant_id>RF1 NS109583</funding_grant_id><funding_grant_id>R01 NS088596</funding_grant_id><pubmed_authors>Hersh J</pubmed_authors><pubmed_authors>Prah J</pubmed_authors><pubmed_authors>Liu R</pubmed_authors><pubmed_authors>Yang SH</pubmed_authors><pubmed_authors>Winters A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modulation of astrocyte phenotype in response to T-cell interaction.</name><description>We determined that T-cell astrocyte interaction modulates interleukin-10 (IL-10) production from both cell types. The impact of IL-10 on astrocytes was compared to IL-10 generated from T-cell-astrocyte interactions in vitro. We demonstrated that T-cells directly interact with astrocytes to upregulate gene expression and secretion of IL-10, confirmed by elevated STAT3p/STAT3 expression in astrocytes. IL-10 increased astrocytes proliferation. In addition, IL-10 treatment and CD4+ co-culture shifts primary astrocytes toward a more energetic phenotype. These findings indicate that direct interaction of CD4+ T-cells with astrocytes, activated the IL-10 anti-inflammatory pathway, altering astrocyte phenotype, metabolism, and proliferation.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2025-04-04T02:25:16.868Z</modification><creation>2025-04-04T02:25:16.868Z</creation></dates><accession>S-EPMC7856103</accession><cross_references><pubmed>33370671</pubmed><doi>10.1016/j.jneuroim.2020.577455</doi></cross_references></HashMap>