Laboratory of Fish Molecular Immunology, College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China.
Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
Front Immunol. 2021 Mar 31;12:617753. doi: 10.3389/fimmu.2021.617753. eCollection 2021.
Pathogen infection can cause the production of inflammatory cytokines, which are key mediators that cause the host's innate immune response. Therefore, proper regulation of immune genes associated with inflammation is essential for immune response. Among them, microRNAs (miRNAs) as gene regulator have been widely reported to be involved in the innate immune response of mammals. However, the regulatory network in which miRNAs are involved in the development of inflammation is largely unknown in lower vertebrates. Here, we identified two miRNAs from miiuy croaker (), miR-210 and miR-3570, which play a negative regulatory role in host antibacterial immunity. We found that the expressions of miR-210 and miR-3570 were significantly upregulated under the stimulation of Gram-negative bacterium and LPS (lipopolysaccharide). Induced miR-210 and miR-3570 inhibit inflammatory cytokine production by targeting RIPK2, thereby avoiding excessive inflammation. In particular, we found that miR-210 and miR-3570 negatively regulate antimicrobial immunity by regulating the RIPK2-mediated NF-κB signaling pathway. The collective results indicated that both miRNAs are used as negative feedback regulators to regulate RIPK2-mediated NF-κB signaling pathway and thus play a regulatory role in bacteria-induced inflammatory response.
病原体感染可导致炎症细胞因子的产生,而这些细胞因子是宿主固有免疫反应的关键介质。因此,适当调节与炎症相关的免疫基因对于免疫反应至关重要。其中,microRNAs(miRNAs)作为基因调节剂,已被广泛报道参与哺乳动物的固有免疫反应。然而,miRNAs 参与炎症发展的调控网络在低等脊椎动物中很大程度上是未知的。在这里,我们从米氏绒螯蟹()中鉴定出了两种 miRNA,miR-210 和 miR-3570,它们在宿主抗菌免疫中起负调控作用。我们发现,在革兰氏阴性菌 和 LPS(脂多糖)的刺激下,miR-210 和 miR-3570 的表达显著上调。诱导的 miR-210 和 miR-3570 通过靶向 RIPK2 抑制炎症细胞因子的产生,从而避免过度炎症。特别是,我们发现 miR-210 和 miR-3570 通过调节 RIPK2 介导的 NF-κB 信号通路来负调控抗菌免疫。这些结果表明,这两种 miRNA 被用作负反馈调节剂来调节 RIPK2 介导的 NF-κB 信号通路,从而在细菌诱导的炎症反应中发挥调节作用。