ADP ribosylation of human neutrophil peptide-1 regulates its biological properties

作者：Gregorino Paone, Akihiro Wada, Linda A. Stevens, Abul Bashar Md Abdul Matin, Toshiya Hirayama, Rodney L. Levine, Joel Moss · 发表于：Proceedings of the National Academy of Sciences · 年份：2002 · DOI：10.1073/pnas.122238899 · 被引用次数：123 · 研究领域：Antimicrobial Peptides and Activities、Toxin Mechanisms and Immunotoxins、PARP inhibition in cancer therapy

In human airways, epithelial cells lining the lumen and intraluminal cells (e.g., polymorphonuclear cells) participate in the innate immune response. These cells secrete or express on their surfaces arginine-specific ADP ribosyltransferases. Defensins, antimicrobial proteins secreted by immune cells, are arginine-rich, leading us to hypothesize that ADP ribosylation could modify their biological activities. We found that an arginine-specific ADP ribosyltransferase-1 present on airway epithelial cells modifies Arg-14 of alpha defensin-1. ADP-ribosylated defensin-1 had decreased antimicrobial and cytotoxic activities but still stimulated T cell chemotaxis and IL-8 release from A549 cells. Further, ADP-ribosylated defensin-1 inhibited cytotoxic and antimicrobial activities of unmodified defensin-1. We identified ADP-ribosylated defensin-1 in bronchoalveolar lavage fluid from smokers but not from nonsmokers, confirming its existence in vivo. Thus, airway mono-ADP-ribosyltransferases could have an important regulatory role in the innate immune response through modification of alpha defensin-1 and perhaps other basic molecules, with alteration of their biological properties.