| Literature DB >> 29909986 |
Paul K Ziegler1, Julia Bollrath2, Charles K Pallangyo2, Takaji Matsutani3, Özge Canli2, Tiago De Oliveira2, Michaela A Diamanti2, Nina Müller2, Jaba Gamrekelashvili4, Tracy Putoczki5, David Horst6, Arun K Mankan2, Meryem G Öner7, Susanna Müller7, Josef Müller-Höcker7, Thomas Kirchner8, Julia Slotta-Huspenina9, M Mark Taketo10, Thomas Reinheckel11, Stefan Dröse12, Andrew C Larner13, Winfried S Wels14, Matthias Ernst15, Tim F Greten16, Melek C Arkan17, Thomas Korn18, Dagmar Wirth19, Florian R Greten20.
Abstract
In colorectal cancer patients, a high density of cytotoxic CD8+ T cells in tumors is associated with better prognosis. Using a Stat3 loss-of-function approach in two wnt/β-catenin-dependent autochthonous models of sporadic intestinal tumorigenesis, we unravel a complex intracellular process in intestinal epithelial cells (IECs) that controls the induction of a CD8+ T cell based adaptive immune response. Elevated mitophagy in IECs causes iron(II)-accumulation in epithelial lysosomes, in turn, triggering lysosomal membrane permeabilization. Subsequent release of proteases into the cytoplasm augments MHC class I presentation and activation of CD8+ T cells via cross-dressing of dendritic cells. Thus, our findings highlight a so-far-unrecognized link between mitochondrial function, lysosomal integrity, and MHC class I presentation in IECs and suggest that therapies triggering mitophagy or inducing LMP in IECs may prove successful in shifting the balance toward anti-tumor immunity in colorectal cancer.Entities:
Keywords: Stat3; adaptive immunity; antigen processing; colon cancer; cross dressing; intestinal epithelial cells; lysosomal membrane permeabilization; mitophagy
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Year: 2018 PMID: 29909986 PMCID: PMC6354256 DOI: 10.1016/j.cell.2018.05.028
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582