The novel fish miRNA, Soc-miR-118, functions as a negative regulator in NF-κB-mediated inflammation by targeting IL-6 in teleost fish

Int J Biol Macromol. 2024 Jun;269(Pt 1):132100. doi: 10.1016/j.ijbiomac.2024.132100. Epub 2024 May 4.

Abstract

Inflammation is initiated as a protective response of the organism to remove invading bacterial and initiate the healing process. Prolonged inflammation and excessive production of inflammatory cytokines lead to inflammatory disorders or autoimmune diseases. Thus, different layers of negative regulators are needed to achieve balances between protective immunity and inflammatory pathology. Accumulating evidences show that miRNAs act as significant and multifunctional regulators involved in regulating networks of host-pathogen interactions. However, the functions and mechanisms of miRNAs in directly targeting and regulating inflammatory cytokines remains largely unknown in lower vertebrates. In this study, we report a novel miRNA, Soc-miR-118, identified from Sciaenops ocellatus, which plays a negative role in antibacterial immunity by regulating Interleukin-6 (IL-6). Specifically, we found that Soc-miR-118 directly targets IL-6 and suppresses the production of inflammatory cytokines through the NF-κB signaling pathway, thereby avoiding excessive inflammatory response. Particularly, the mechanism by which Soc-miR-118 regulates IL-6 expression also exist in other fish, suggesting that the miRNA in fish has evolutionarily conserved regulatory systems. The collective results that Soc-miR-118 acts as a negative regulator involved in host antibacterial immunity through directly regulating inflammatory cytokines, will greatly enrich the intricate networks of host-pathogen interaction in lower vertebrates.

Keywords: Inflammation; Interleukin-6; miRNA.

MeSH terms

  • Animals
  • Fishes / genetics
  • Fishes / immunology
  • Fishes / microbiology
  • Gene Expression Regulation
  • Inflammation* / genetics
  • Interleukin-6* / genetics
  • Interleukin-6* / metabolism
  • MicroRNAs* / genetics
  • NF-kappa B* / metabolism
  • Signal Transduction

Substances

  • MicroRNAs
  • Interleukin-6
  • NF-kappa B