| Literature DB >> 30063264 |
Debra K Newman1,2,3, Guoping Fu1, Laura McOlash4, David Schauder3, Peter J Newman1,5, Weiguo Cui1,3, Sridhar Rao1,5, Bryon D Johnson3,4, Jill A Gershan4, Matthew J Riese1,3,6.
Abstract
Inhibitory cell surface proteins on T cells are often dynamically regulated, which contributes to their physiologic function. PECAM-1 (CD31) is an inhibitory receptor that facilitates TGF-β-mediated suppression of T cell activity. It is well established in CD4+ T cells that PECAM-1 is expressed in naïve recent thymic emigrants, but is down-regulated after acute T cell activation and absent from memory cells. The extent to which PECAM-1 expression is similarly regulated in CD8+ T cells is much less well characterized. We evaluated T cells recovered from mice after infection with a model intracellular pathogen and determined that, in CD8+ T cells, PECAM-1 expression was strongly down-regulated during acute infection but re-expressed to intermediate levels in memory cells. Down-regulation of PECAM-1 expression in CD8+ T cells was transcriptionally regulated and affected by the strength and nature of TCR signaling. PECAM-1 was also detected on the surface of human activated/memory CD8+ , but not CD4+ T cells. These data demonstrate that PECAM-1 expression is dynamically regulated, albeit differently, in both CD4+ and CD8+ T cells. Furthermore, unlike memory CD4+ T cells, memory CD8+ T cells retain PECAM-1 expression and have the potential to be modulated by this inhibitory receptor. ©2018 Society for Leukocyte Biology.Entities:
Keywords: CD8+ T cell; Listeria monocytogenes; PECAM-1; diacylglycerol kinase zeta
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Year: 2018 PMID: 30063264 PMCID: PMC6195461 DOI: 10.1002/JLB.2HI0617-229RRR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962