Objective

AUTHOR=Hiramatsu-Asano Sumie , Sunahori-Watanabe Katsue , Zeggar Sonia , Katsuyama Eri , Mukai Tomoyuki , Morita Yoshitaka , Wada Jun TITLE=Deletion of Mir223 Exacerbates Lupus Nephritis by Targeting S1pr1 in Faslpr/lpr Mice JOURNAL=Frontiers in Immunology VOLUME=11 YEAR=2021 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2020.616141 DOI=10.3389/fimmu.2020.616141 ISSN=1664-3224 ABSTRACT=Objective

The micro RNAs (miRNAs) and their target mRNAs are differentially expressed in various immune-mediated cells. Here, we investigated the role of Mir223 and sphingosine-1-phosphate receptor 1 (S1pr1) in the pathogenesis of systemic lupus erythematosus.

Methods

We analyzed miRNA and mRNA profiling data of CD4⁺ splenic T cells derived from MRL/MpJ-Fas^lpr/J mice. We performed 3′ untranslated region (UTR) luciferase reporter gene assay using human umbilical vein endothelial cells (HUVECs). We generated the B6-Mir223^−/−Fas^lpr/lpr mice and the lupus phenotypes were analyzed.

Results

In CD4⁺ splenic T cells, we identified upregulation of miR-223-3p and downregulation of the possible target, S1pr1 by RNA sequencing of MRL/MpJ-Fas^lpr/J mice. The transfection with miR-223-3p mimic significantly suppressed a luciferase activity in HUVEC treated with a Lentivirus vector containing 3′ UTR of S1pr1. The mRNA levels of S1pr1 were significantly decreased after miR-223-3p overexpression. In B6-Mir223^−/−Fas^lpr/lpr mice, the proportion of CD3⁺ T cells, CD3⁺CD4^-CD8⁻ cells, B cells, plasma cells, and S1PR1⁺CD4⁺ T cells in the spleen was significantly increased compared with that in B6-Mir223^+/+Fas^lpr/lpr mice by flow cytometry. B6-Mir223^−/−Fas^lpr/lpr mice demonstrated the elevation of glomerular and renal vascular scores associated with enhanced intraglomerular infiltration of S1PR1⁺CD4⁺ T cells.

Conclusion

Unexpectedly, the deletion of Mir223 exacerbated the lupus phenotypes associated with increased population of S1PR1⁺CD4⁺ T in spleen and the enhanced infiltration of S1PR1⁺CD4⁺ T cells in inflamed kidney tissues, suggesting compensatory role of Mir223 in the pathogenesis of lupus nephritis.