AUTHOR=Kuttke Mario , Hromadová Dominika , Yildirim Ceren , Brunner Julia S. , Vogel Andrea , Paar Hannah , Peters Sophie , Weber Maria , Hofmann Melanie , Kerndl Martina , Kieler Markus , Datler Hannes , Musiejovsky Laszlo , Salzmann Manuel , Lang Michaela , Soukup Klara , Halfmann Angela , Sharif Omar , Schabbauer Gernot 

TITLE=PI3K Signaling in Dendritic Cells Aggravates DSS-Induced Colitis

JOURNAL=Frontiers in Immunology

VOLUME=13

YEAR=2022

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2022.695576

DOI=10.3389/fimmu.2022.695576

ISSN=1664-3224

ABSTRACT=<p>Aberrant innate immune responses to the gut microbiota are causally involved in the pathogenesis of inflammatory bowel diseases (IBD). The exact triggers and main signaling pathways activating innate immune cells and how they modulate adaptive immunity in IBD is still not completely understood. Here, we report that the PI3K/PTEN signaling pathway in dendritic cells enhances IL-6 production in a model of DSS-induced colitis. This results in exacerbated Th1 cell responses and increased mortality in DC-specific PTEN knockout (PTEN<sup>ΔDC</sup>) animals. Depletion of the gut microbiota using antibiotics as well as blocking IL-6R signaling rescued mortality in PTEN<sup>ΔDC</sup> mice, whereas adoptive transfer of Flt3L-derived PTEN<sup>-/-</sup> DCs into WT recipients exacerbated DSS-induced colitis and increased mortality. Taken together, we show that the PI3K signaling pathway in dendritic cells contributes to disease pathology by promoting IL-6 mediated Th1 responses.</p>