Antimicrobial Peptide CATH-2 Attenuates Avian Pathogenic E. coli-Induced Inflammatory Response via NF-κB/NLRP3/MAPK Pathway and Lysosomal Dysfunction in Macrophages

Int J Mol Sci. 2024 Nov 22;25(23):12572. doi: 10.3390/ijms252312572.

Abstract

Cathelicidins have anti-inflammatory activity and chicken cathelicidin-2 (CATH-2) has shown to modulate immune response, but the underlying mechanism of its anti-inflammation is still unclear. Therefore, in this study, we investigated the anti-inflammatory activity of CATH-2 on murine peritoneal macrophages during avian pathogenic E. coli (APEC) infection. The results showed that CATH-2 priming significantly reduced the production of IL-1β, IL-6, IL-1α, and IL-12. In addition, CATH-2 significantly attenuated APEC-induced caspase-1 activation and the formation of an adaptor (ASC) of NLRP3 inflammasome, indicating that CATH-2 inhibits APEC-induced NLRP3 inflammasome activation. Furthermore, CATH-2 remarkably inhibited NF-κB and MAPK signaling pathways activation. Moreover, CATH-2 significantly inhibited mRNA expression of cathepsin B and inhibited lysosomal acidification, demonstrating that CATH-2 disrupts lysosomal function. In addition, promoting lysosomal acidification using ML-SA1 hampered the anti-inflammatory effect of CATH-2 on APEC-infected cells. In conclusion, our study reveals that CATH-2 inhibits APEC-induced inflammation via the NF-κB/NLRP3/MAPK pathway through the dysfunction of lysosome.

Keywords: NF-κB/NLRP3/MAPK pathway; anti-inflammatory response; avian pathogenic E. coli; cathelicidin-2.

MeSH terms

  • Animals
  • Antimicrobial Peptides / metabolism
  • Antimicrobial Peptides / pharmacology
  • Cathelicidins*
  • Chickens
  • Escherichia coli Infections* / metabolism
  • Escherichia coli Infections* / microbiology
  • Escherichia coli*
  • Inflammasomes / metabolism
  • Inflammation / metabolism
  • Lysosomes* / metabolism
  • MAP Kinase Signaling System / drug effects
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / metabolism
  • Mice
  • NF-kappa B* / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
  • Signal Transduction / drug effects

Substances

  • NLR Family, Pyrin Domain-Containing 3 Protein
  • NF-kappa B
  • Cathelicidins
  • Inflammasomes
  • Nlrp3 protein, mouse
  • Antimicrobial Peptides