| Literature DB >> 31723060 |
Bo Sun1,2, Hui-Hsin Chang1,2, Ari Salinger3, Beverly Tomita1,2, Mandar Bawadekar4, Caitlyn L Holmes4,5, Miriam A Shelef4,6, Eranthie Weerapana7, Paul R Thompson3, I-Cheng Ho1,2.
Abstract
Dysregulated citrullination, a unique form of posttranslational modification catalyzed by the peptidylarginine deiminases (PADs), has been observed in several human diseases, including rheumatoid arthritis. However, the physiological roles of PADs in the immune system are still poorly understood. Here, we report that global inhibition of citrullination enhances the differentiation of type 2 helper T (Th2) cells but attenuates the differentiation of Th17 cells, thereby increasing the susceptibility to allergic airway inflammation. This effect on Th cells is due to inhibition of PAD2 but not PAD4. Mechanistically, PAD2 directly citrullinates GATA3 and RORγt, 2 key transcription factors determining the fate of differentiating Th cells. Citrullination of R330 of GATA3 weakens its DNA binding ability, whereas citrullination of 4 arginine residues of RORγt strengthens its DNA binding. Finally, PAD2-deficient mice also display altered Th2/Th17 immune response and heightened sensitivity to allergic airway inflammation. Thus, our data highlight the potential and caveat of PAD2 as a therapeutic target of Th cell-mediated diseases.Entities:
Keywords: Adaptive immunity; Allergy; Autoimmunity; Immunology; T cells
Year: 2019 PMID: 31723060 PMCID: PMC6948856 DOI: 10.1172/jci.insight.129687
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708