Identification of a lncRNA/circRNA-miRNA-mRNA network to explore the effects of ricin toxin-induced inflammation in RAW264.7 cells

蓖麻毒素 小RNA 竞争性内源性RNA 核糖核酸 生物 信号转导 炎症 细胞生物学 信使核糖核酸 长非编码RNA 基因 分子生物学 计算生物学 毒素 遗传学 免疫学
作者
Kaikai Yu,Haotian Yu,Yingshuang Wang,Mingxin Dong,Yan Wang,Na Zhao,Jianxu Zhang,Chengbiao Sun,Na Xu,Wensen Liu
出处
期刊:Toxicon [Elsevier]
卷期号:203: 129-138 被引量:5
标识
DOI:10.1016/j.toxicon.2021.10.007
摘要

Ricin toxin (RT) is a ribosome-inactivating protein derived from the beans of the castor oil plant. Our previous studies have reported that RT can induce the production of inflammatory cytokines and cause inflammatory injury in RAW264.7 cells. In order to explore the various biological processes that long noncoding RNA (lncRNA), circular RNA (circRNA) and micro RNA (miRNA) as endogenous non-coding RNAs (ceRNAs) may participate in the pro-inflammatory mechanism, RT (20 ng/mL) treated and normal RAW264.7 cells were firstly sequenced by RNA-seq. By comparing the differentially expressed genes, we obtained 10 hub genes and enriched the inflammatory-related signaling pathways. Based on our results, we concluded a lncRNA/circRNA-miRNA-mRNA network. Finally, we verified the key genes and pathways by qRT-PCR, WB and ELISA. From the experiment results, an opening MAPK signaling pathway in TNF signaling pathway via TNFR2 was found involved in RT-induced inflammation. This work provides a reference for searching for ceRNA targets or therapeutic drugs in RT-induced inflammatory injury in the future. • Four sequencing data sets in ricin toxin-mediated inflammatory injury were reported. • The inflammatory related function of mmu-miR-5114 and mmu-miR-1930–3p was identified. • An opening MAPK signaling pathway was identified clearly in TNF signaling pathway via TNFR2.
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