| Literature DB >> 29654208 |
Justin P Ingram1, Sarah Tursi2, Ting Zhang1, Wei Guo3,4, Chaoran Yin1, Meghan A Wynosky-Dolfi5, Joris van der Heijden6, Kathy Q Cai7, Masahiro Yamamoto8, B Brett Finlay6, Igor E Brodsky5, Sergei I Grivennikov3, Çagla Tükel2, Siddharth Balachandran9.
Abstract
The cytokine IFN-γ has well-established antibacterial properties against the bacterium Salmonella enterica in phagocytes, but less is known about the effects of IFN-γ on Salmonella-infected nonphagocytic cells, such as intestinal epithelial cells (IECs) and fibroblasts. In this article, we show that exposing human and murine IECs and fibroblasts to IFN-γ following infection with Salmonella triggers a novel form of cell death that is neither pyroptosis nor any of the major known forms of programmed cell death. Cell death required IFN-γ-signaling via STAT1-IRF1-mediated induction of guanylate binding proteins and the presence of live Salmonella in the cytosol. In vivo, ablating IFN-γ signaling selectively in murine IECs led to higher bacterial burden in colon contents and increased inflammation in the intestine of infected mice. Together, these results demonstrate that IFN-γ signaling triggers release of Salmonella from the Salmonella-containing vacuole into the cytosol of infected nonphagocytic cells, resulting in a form of nonpyroptotic cell death that prevents bacterial spread in the gut.Entities:
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Year: 2018 PMID: 29654208 PMCID: PMC6034694 DOI: 10.4049/jimmunol.1701386
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422