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dc.contributor.authorDai, Rujuanen
dc.contributor.authorHeid, Bettinaen
dc.contributor.authorXu, Xiguangen
dc.contributor.authorXie, Hehuang Daviden
dc.contributor.authorReilly, Christopher M.en
dc.contributor.authorAhmed, S. Ansaren
dc.date.accessioned2020-07-13T11:46:49Zen
dc.date.available2020-07-13T11:46:49Zen
dc.date.issued2020-07-09en
dc.identifier.citationBMC Immunology. 2020 Jul 09;21(1):41en
dc.identifier.urihttp://hdl.handle.net/10919/99343en
dc.description.abstractBackground Recent studies have shown that early growth response 2 (EGR2) is highly induced in activated T cells and regulates T cell functions. In normal C57BL/6 (B6) mice, deletion of EGR2 in lymphocytes results in the development of lupus-like systemic autoimmune disease, which implies indirectly an autoimmune protective role of EGR2. Conversely, increased EGR2 gene expression is suggested to link with high risk of human lupus. In the present studies we sought to clarify the expression and inflammation regulatory role of EGR2 in murine lupus T cells directly. Results We performed RT-qPCR analysis and found a significant increase of EGR2 mRNA expression in human lupus PBMCs and in CD4+ T cells from three different murine lupus models including MRL-lpr, B6-lpr, and B6.sle123 mice at diseased stage when compared to age-matched control MRL or B6 mice. By performing intracellular flow cytometry analysis, we found that EGR2 protein expression was significantly increased in resting lupus (either MRL-lpr or B6.sle123) CD4+ T cells when compared to CD4+ T cells from their respective non-autoimmune controls. However, there was no difference of EGR2 protein expression in anti-CD3 and anti-CD28 stimulated control and lupus CD4+ T cells since there was a stronger induction of EGR2 in activated control CD4+ T cells. EGR2 expression was significantly increased in MRL-lpr mice at an age when lupus is manifested. To understand further the function of elevated EGR2 in lupus CD4+ T cells, we inhibited EGR2 with a specific siRNA in vitro in splenocytes from MRL-lpr and control MRL mice at 15 weeks-of-age. We found that EGR2 inhibition significantly reduced IFNγ production in PMA and ionomycin activated MRL-lpr lupus CD4+ T cells, but not control MRL CD4+ T cells. We also found that inhibition of EGR2 in vitro suppressed the Th1 differentiation in both MRL and MRL-lpr naïve CD4+ T cells. Conclusions EGR2 is highly upregulated in human and murine lupus cells. Our in vitro data suggest a positive role of EGR2 in the regulation of Th1 differentiation and IFNγ production in lupus effector CD4+ T cells.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleEGR2 is elevated and positively regulates inflammatory IFNγ production in lupus CD4+ T cellsen
dc.typeArticle - Refereeden
dc.date.updated2020-07-12T03:50:55Zen
dc.description.versionPublished versionen
dc.rights.holderThe Author(s)en
dc.contributor.departmentBiological Sciencesen
dc.contributor.departmentBiomedical Sciences and Pathobiologyen
dc.contributor.departmentFralin Life Sciences Instituteen
dc.title.serialBMC Immunologyen
dc.identifier.doihttps://doi.org/10.1186/s12865-020-00370-zen
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Creative Commons Attribution 4.0 International
License: Creative Commons Attribution 4.0 International