RAGE participates in the intracellular transport of Campylobacter jejuni cytolethal distending toxin

J Microbiol Immunol Infect. 2024 Oct;57(5):709-719. doi: 10.1016/j.jmii.2024.07.007. Epub 2024 Aug 3.

Abstract

Background: Cytolethal distending toxin (CDT) belongs to the genotoxin family and is closely related to Campylobacter jejuni-associated gastroenteritis. We recently reported that CDT triggers the danger-associated molecular pattern (DAMP) signaling to exert deleterious effects on host cells. However, how CDT traffics in cells and the mechanism of CDT intoxication remain to be elucidated.

Methods: Recombinant CDT subunits (CdtA, CdtB, and CdtC) were purified, and their activity was characterized in gastrointestinal cells. Molecular approaches and image tracking were employed to analyze the delivery of CDT in host cells.

Results: In this study, we found that CDT interacts with the receptor of advanced glycation end products (RAGE) and high mobility group box 1 (HMGB1) to enter the cells. Our results further showed that CdtB transport in cells through the dynamin-dependent endocytic pathway and lysosome is involved in this process. Conversely, blockage of RAGE signaling resulted in a reduction in CDT-arrested cell cycles, indicating that RAGE is involved in CDT intracellular transport and its subsequent pathogenesis.

Conclusion: Our results demonstrate that RAGE is important for CDT trafficking in the cells. These findings expand our understanding of important issues related to host cell intoxication by C. jejuni CDT.

Keywords: Campylobacter jejuni; Cytolethal distending toxin; Intracellular transport.

MeSH terms

  • Animals
  • Bacterial Toxins* / metabolism
  • Campylobacter jejuni* / metabolism
  • Endocytosis
  • HMGB1 Protein / metabolism
  • Humans
  • Protein Transport
  • Receptor for Advanced Glycation End Products* / metabolism
  • Signal Transduction

Substances

  • cytolethal distending toxin
  • Bacterial Toxins
  • Receptor for Advanced Glycation End Products
  • HMGB1 Protein
  • HMGB1 protein, human