Myeloperoxidase-dependent tyrosine halogenation potentiates alpha-defensins functions
bioRxiv (Cold Spring Harbor Laboratory)(2023)
摘要
Neutrophils are immune cells specialized in detecting and eliminating microbes through potent cytotoxic mechanisms. Most of the neutrophil antimicrobial proteins are stored in intracellular organelles called granules, which are rapidly mobilized to direct the neutrophil cytotoxic machinery against the microbe. However, it remains unclear how the cytotoxic mechanisms cooperate with each other to minimize self-damage and allow an efficient immune response. Here we show that after neutrophil activation, highly oxidative myeloperoxidase-derived hypohalous acids target the antimicrobial peptides alpha-defensin 1-3, leading to chlorination of tyrosine 21 and iodination of tyrosine 16. We observe alpha-defensin 1-3 halogenation in rat neutrophils, and notably, in sputum samples from Cystic Fibrosis patients as well as in Streptococcus pneumoniae bronchoalveolar lavage (BAL) and Staphylococcus aureus skin abscesses infected patients. Importantly, halogenated alpha-defensins are more efficient immunomodulators and anti-toxin mediators than the non-modified peptides, indicating that this rare post-translational modification is important for inflammation.
### Competing Interest Statement
The authors have declared no competing interest.
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关键词
myeloperoxidase-dependent,alpha-defensins
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