AUTHOR=Wasén Caroline , Ospelt Caroline , Camponeschi Alessandro , Erlandsson Malin C. , Andersson Karin M. E. , Silfverswärd Sofia Töyrä , Gay Steffen , Bokarewa Maria I. TITLE=Nicotine Changes the microRNA Profile to Regulate the FOXO Memory Program of CD8+ T Cells in Rheumatoid Arthritis JOURNAL=Frontiers in Immunology VOLUME=11 YEAR=2020 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2020.01474 DOI=10.3389/fimmu.2020.01474 ISSN=1664-3224 ABSTRACT=

Objective: Smoking suppresses PD-1 expression in patients with rheumatoid arthritis (RA). In this study, we assess if smoking changed the epigenetic control over CD8⁺ T cell memory formation through a microRNA (miR) dependent mechanism.

Methods: Phenotypes of CD8⁺ T cells from smokers and non-smokers, RA and healthy, were analyzed by flow cytometry. A microarray analysis was used to screen for differences in miR expression. Sorted CD8⁺ cells were in vitro stimulated with nicotine and analyzed for transcription of miRs and genes related to memory programming by qPCR.

Results: CD27⁺CD107a⁻CD8⁺ T cells, defining a naïve-memory population, had low expression of PD-1. Additionally, the CD27⁺ population was more frequent in smokers (p = 0.0089). Smokers were recognized by differential expression of eight miRs. Let-7c-5p, let-7d-5p and let-7e-5p, miR-92a-3p, miR-150-5p, and miR-181-5p were up regulated, while miR-3196 and miR-4723-5p were down regulated. These miRs were predicted to target proteins within the FOXO-signaling pathway involved in CD8⁺ memory programming. Furthermore, miR-92a-3p was differentially expressed in CD8⁺ cells with naïve-memory predominance. Nicotine exposure of CD8⁺ cells induced the expression of miR-150-5p and miR-181a-5p in the naïve-memory cells in vitro. Additionally, nicotine exposure inverted the ratio between mRNAs of proteins in the FOXO pathway and their targeting miRs.

Conclusions: Smokers have a high prevalence of CD8⁺ T cells with a naïve-memory phenotype. These cells express a miR profile that interacts with the memory programming conducted through the FOXO pathway.