作者
Marlene Schwarzfischer,Anna Niechcial,Kristina Handler,Yasser Morsy,Marcin Wawrzyniak,Andrea S. Laimbacher,Kirstin Atrott,Roberto Manzini,Katharina Baebler,Larissa Hering,Egle Katkeviciutė,Janine Häfliger,Silvia Lang,Maja E Keller,Jérôme Woodtli,Lisa Eisenbeiss,Thomas Kræmer,Elisabeth M. Schraner,Mahesa Wiesendanger,Sebastian Zeißig,Gerhard Rogler,Andreas E. Moor,Michael Scharl,Marianne R. Spalinger
摘要
Objective Inflammatory bowel disease (IBD) is a multifactorial condition driven by genetic and environmental risk factors. A genetic variation in the protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene has been associated with autoimmune disorders while protecting from the IBD subtype Crohn’s disease. Mice expressing the murine orthologous PTPN22-R619W variant are protected from intestinal inflammation in the model of acute dextran sodium sulfate (DSS)-induced colitis. We previously identified food-grade titanium dioxide (TiO 2 , E171) as a neglected IBD risk factor. Here, we investigate the interplay of the PTPN22 variant and TiO 2 -mediated effects during IBD pathogenesis. Design Acute DSS colitis was induced in wild-type and PTPN22 variant mice (PTPN22-R619W) and animals were treated with TiO 2 nanoparticles during colitis induction. Disease-triggering mechanisms were investigated using bulk and single-cell RNA sequencing. Results In mice, administration of TiO 2 nanoparticles abrogated the protective effect of the variant, rendering PTPN22-R619W mice susceptible to DSS colitis. In early disease, cytotoxic CD8 + T-cells were found to be reduced in the lamina propria of PTPN22-R619W mice, an effect reversed by TiO 2 administration. Normalisation of T-cell populations correlated with increased Ifng expression and, at a later stage of disease, the promoted prevalence of proinflammatory macrophages that triggered severe intestinal inflammation. Conclusion Our findings indicate that the consumption of TiO 2 nanoparticles might have adverse effects on the gastrointestinal health of individuals carrying the PTPN22 variant. This demonstrates that environmental factors interact with genetic risk variants and can reverse a protective mechanism into a disease-promoting effect.