Title (en)
Dynamic miRNA profile of host T cells during early hepatic stages of Schistosoma japonicum infection
Language
English
Description (en)
Schistosomes undergo complicated migration in final hosts during infection, associated with differential immune responses. It has been shown that CD4+ T cells play critical roles in response to Schistosoma infections and accumulated documents have indicated that miRNAs tightly regulate T cell activity. However, miRNA profiles in host T cells associated with Schistosoma infection remain poorly characterized. Therefore, we undertook the study and systematically characterized T cell miRNA profiles from the livers and blood of S. japonicum infected C57BL/6J mice at 14- and 21-days post-infection. We observed 508 and 504 miRNAs, in which 264 miRNAs were co-detected in T cells isolated from blood and livers, respectively. The comparative analysis of T cell miRNAs from uninfected and infected C57BL/6J mice blood showed that miR-486b-5p/3p expression was significantly downregulated and linked to various T cell immune responses and miR-375-5p was highly upregulated, associated with Wnt signaling and pluripotency, Delta notch signaling pathways, etc. Whereas hepatic T cells showed miR-466b-3p, miR-486b-3p, miR-1969, and miR-375 were differentially expressed compared to the uninfected control. The different expressions of some miRNAs were further corroborated in isolated T cells from mice and in vitro cultured EL-4 cells treated with S. japonicum worm antigens by RT-qPCR and similar results were found. In addition, bioinformatics analysis combined with RT-qPCR validation of selected targets associated with the immune system and parasite-caused infectious disease showed a significant increase in the expression of Ctla4, Atg5, Hgf, Vcl and Arpc4 and a decreased expression of Fermt3, Pik3r1, Myd88, Nfkbie, Ppp1r12a, Ppp3r1, Nfyb, Atg12, Ube2n, Tyrobp, Cxcr4 and Tollip. Overall, these results unveil the comprehensive repertoire of T cell miRNAs during S. japonicum infection, suggesting that the circulatory (blood) and liver systems have distinct miRNAs landscapes that may be important for regulating T cell immune response. Altogether, our findings indicated a dynamic expression pattern of T cell miRNAs during the hepatic stages of S. japonicum infection.
Keywords (en)
Microrna Regulation; Differentiation; Mansoni; Cd4(+); Gene; Biogenesis; Expression; Apoptosis; Migration; Responses
DOI
10.3389/fimmu.2022.911139
Author of the digital object
Bikash R. Giri (Tongji University School of Medicine Shanghai)
Guofeng Cheng (Tongji University School of Medicine Shanghai)
Maria Y. Pakharukova (Siberian Branch of Russian Academy of Sciences / Novosibirsk State University / Institute of Molecular Biology and Biophysics Novosibirsk)
Shi Yan (University of Veterinary Medicine Vienna)
Lin Qiu (Chinese Academy of Agricultural Sciences)
Chuantao Fang (Tongji University School of Medicine Shanghai)
Shun Li (Chinese Academy of Agricultural Sciences)
Format
application/pdf
Size
611.5 kB
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Type of publication
Article
Name of Publication (en)
Frontiers in Immunology
Pages or Volume
15
Volume
13
Publisher
Frontiers Media Sa
Publication Date
2022
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Persistent identifier
DOI
https://phaidra.vetmeduni.ac.at/o:2081
https://doi.org/10.3389/fimmu.2022.911139 - Content
- DetailsObject typePDFDocumentFormatapplication/pdfCreated08.09.2023 11:20:06 UTC
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