The deficiency of DNASE1L3 does not affect systemic sclerosis pathogenesis in two inducible murine models of the disease
Open Access
- 4 April 2024
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 54 (6) , e2350903
Abstract
We induced systemic sclerosis (SSc)-like disease in both wild-type and Dnase1l3-deficient mice using two distinct approaches involving bleomycin and hypochlorous acid injections. Our observations revealed that the deficiency in DNASE1L3 did not affect tissue fibrosis or inflammation caused by these treatments. Despite the association of single nucleotide polymorphisms in humans with SSc pathogenesis, our study demonstrates that DNASE1L3 is dispensable in two inducible murine models of SSc-like pathogenesis.Keywords
Funding Information
- Fondation pour la Recherche Médicale
This publication has 10 references indexed in Scilit:
- Reduced digestion of circulating genomic DNA in systemic sclerosis patients with the DNASE1L3 R206C variantRheumatology, 2023
- Arg206Cys substitution in DNASE1L3 causes a defect in DNASE1L3 protein secretion that confers risk of systemic lupus erythematosusAnnals of the Rheumatic Diseases, 2021
- The Role of Nucleases and Nucleic Acid Editing Enzymes in the Regulation of Self-Nucleic Acid SensingFrontiers in Immunology, 2021
- Plasmacytoid Dendritic Cells and Type I Interferon Promote Extrafollicular B Cell Responses to Extracellular Self-DNAImmunity, 2020
- CXCL4 assembles DNA into liquid crystalline complexes to amplify TLR9-mediated interferon-α production in systemic sclerosisNature Communications, 2019
- Plasmacytoid dendritic cells promote systemic sclerosis with a key role for TLR8Science Translational Medicine, 2018
- Digestion of Chromatin in Apoptotic Cell Microparticles Prevents AutoimmunityCell, 2016
- An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3Arthritis Research & Therapy, 2014
- Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic SclerosisThe American Journal of Human Genetics, 2014
- Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzymeClinica Chimica Acta, 2009