Description:
<jats:p>The goal of the present study was to determine whether peptidylarginine deiminase PAD2 and PAD4 enzymes are present in <jats:italic>Balb/c</jats:italic> mouse salivary glands and whether they are able to citrullinate Ro and La ribonucleoproteins. Salivary glands from <jats:italic>Balb/c</jats:italic> mice were cultured in DMEM and supplemented with one of the following stimulants: ATP, LPS, TNF, IFN<jats:italic>γ</jats:italic>, or IL-6. A control group without stimulant was also evaluated. PAD2, PAD4, citrullinated peptides, Ro60, and La were detected by immunohistochemistry and double immunofluorescence. PAD2 and PAD4 mRNAs and protein expression were detected by qPCR and Western blot analysis. PAD activity was assessed using an antigen capture enzyme-linked immunosorbent assay. LPS, ATP, and TNF triggered PAD2 and PAD4 expression; in contrast, no expression was detected in the control group (<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mi>p</mml:mi><mml:mo><</mml:mo><mml:mn>0.001</mml:mn></mml:math>). PAD transcription slightly increased in response to stimulation. Additionally, PAD2/4 activity modified the arginine residues of a reporter protein (fibrinogen) <jats:italic>in vitro</jats:italic>. PADs citrullinated Ro60 and La ribonucleoproteins <jats:italic>in vivo</jats:italic>. Molecular stimulants induced apoptosis in ductal cells and the externalization of Ro60 and La ribonucleoproteins onto apoptotic membranes. PAD enzymes citrullinate Ro and La ribonucleoproteins, and this experimental approach may facilitate our understanding of the role of posttranslational modifications in the pathophysiology of Sjögren’s syndrome.</jats:p>