Citrullination of extracellular histone H3.1 reduces antibacterial activity and exacerbates its proteolytic degradation

J Cyst Fibros. 2021 Mar;20(2):346-355. doi: 10.1016/j.jcf.2020.07.010. Epub 2020 Jul 26.

Abstract

Background: Cystic fibrosis (CF), involves excessive airway accumulation of neutrophils, often in parallel with severe infection caused by Pseudomonas aeruginosa. Free histones are known to possess bactericidal properties, but the degree of antibacterial activity exerted on specific lung-based pathogens is largely unknown. Neutrophils have a high content of peptidyl deiminase 4 (PADI4), which citrullinate cationic peptidyl-arginines. In histone H3.1, several positions in the NH2-terminal tail are subject to citrullination.

Methods: Full-length and segmented histone subunit H3.1 was investigated for bactericidal activity towards P. aeruginosa (strain PAO1). PADI4-induced citrullination of histone H3.1 was assessed for antibacterial activity towards P. aeruginosa. Next, the effect of neutrophil elastase (NE)-mediated proteolysis of histone H3.1 was investigated. Finally, PADI4, H3.1, and citrullinated H3.1 were examined in healthy control and CF patient lung tissues.

Results: Full-length histone H3.1 and sections of the histone H3.1 tail, displayed bactericidal activity towards P. aeruginosa. These antibacterial effects were reduced following citrullination by PADI4 or proteolysis by NE. Interestingly, citrullination of histone H3.1 exacerbated NE-mediated degradation. In CF lung tissue, citrullinated histone H3.1 and PADI4 immunoreactivity was abundant. Degraded histone H3.1 was detected in the sputum of CF patients but was absent in the sputum of healthy controls.

Conclusions: Citrullination impairs the antibacterial activity of histone H3.1 and exacerbates its proteolytic degradation by NE. Citrullination is likely to play an important role during resolution of acute inflammation. However, in chronic inflammation akin to CF, citrullination may dampen host defense and promote pathogen survival, as exemplified by P. aeruginosa.

Keywords: AMPs; Citrullination; Cystic fibrosis; Innate immunity; PADI4; Pseudomonas aeruginosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Citrullination*
  • Cystic Fibrosis / metabolism*
  • Histones / metabolism*
  • Histones / pharmacology*
  • Humans
  • Leukocyte Elastase / metabolism
  • Protein-Arginine Deiminase Type 4 / metabolism*
  • Proteolysis
  • Pseudomonas Infections / drug therapy*
  • Pseudomonas aeruginosa / drug effects

Substances

  • Histones
  • Leukocyte Elastase
  • Protein-Arginine Deiminase Type 4