TCR stimulation without co-stimulatory signals induces expression of “tolerogenic” genes in memory CD4 T cells but does not compromise cell proliferation

•Anti-CD3 mAb stimulation without co-stimulation induces elevated expression of tolerogenic genes, Egr2 and GRAIL, in memory CD4+ T cells.•The high-level expression of Egr2 and GRAIL in memory CD4+ T cells does not abrogate cell proliferation.•Anti-CD3 mAb-stimulated memory CD4+ T cells also express...

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Veröffentlicht in:Molecular immunology 2015-02, Vol.63 (2), p.406-411
Hauptverfasser: Xie, Aini, Zheng, Xiong, Khattar, Mithun, Schroder, Paul, Stepkowski, Stanislaw, Xia, Jiahong, Chen, Wenhao
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Sprache:eng
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Zusammenfassung:•Anti-CD3 mAb stimulation without co-stimulation induces elevated expression of tolerogenic genes, Egr2 and GRAIL, in memory CD4+ T cells.•The high-level expression of Egr2 and GRAIL in memory CD4+ T cells does not abrogate cell proliferation.•Anti-CD3 mAb-stimulated memory CD4+ T cells also expressed high protein/gene levels of phosphorylated STAT5, Nedd4, Bcl-2, and Bcl-XL.•Co-stimulation-independent proliferation of memory CD4+ T cells may be due to elevated expression of molecules that support cell proliferation and survival, but not lack of tolerogenic molecules. Memory T cells resist co-stimulatory blockade and present a unique therapeutic challenge in transplantation and autoimmune diseases. Herein, we determined whether memory T cells express less “tolerogenic” genes than naïve T cells to reinforce a proliferative response under the deprivation of co-stimulatory signals. The expression of ∼40 tolerogenic genes in memory and naïve CD4+ T cells was thus assessed during an in vitro TCR stimulation without co-stimulation. Briefly, upon TCR stimulation with an anti-CD3 mAb alone, memory CD4+ T cells exhibited more proliferation than naïve CD4+ T cells. To our surprise, at 24h upon anti-CD3 mAb stimulation, memory CD4+ T cells expressed more than a 5-fold higher level of the transcription factor Egr2 and a 20-fold higher level of the transmembrane E3 ubiquitin ligase GRAIL than those in naïve T cells. Hence, the high-level expression of tolerogenic genes, Egr2 and GRAIL, in memory CD4+ T cells does not prevent cell proliferation. Importantly, anti-CD3 mAb-stimulated memory CD4+ T cells expressed high protein/gene levels of phosphorylated STAT5, Nedd4, Bcl-2, and Bcl-XL. Therefore, co-stimulation-independent proliferation of memory CD4+ T cells may be due to elevated expression of molecules that support cell proliferation and survival, but not lack of tolerogenic molecules.
ISSN:0161-5890
1872-9142
DOI:10.1016/j.molimm.2014.09.013