Mitophagy in Intestinal Epithelial Cells Triggers Adaptive Immunity during Tumorigenesis

Cell. 2018 Jun 28;174(1):88-101.e16. doi: 10.1016/j.cell.2018.05.028. Epub 2018 Jun 14.

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.

Keywords: Stat3; adaptive immunity; antigen processing; colon cancer; cross dressing; intestinal epithelial cells; lysosomal membrane permeabilization; mitophagy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity* / drug effects
  • Animals
  • Azoxymethane / toxicity
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / drug effects
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Membrane Permeability
  • Colorectal Neoplasms / mortality
  • Colorectal Neoplasms / pathology
  • Cytokines / metabolism
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Female
  • Ferrous Compounds / metabolism
  • Humans
  • Interferon-gamma / metabolism
  • Interferon-gamma / pharmacology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Lysosomes / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Mitophagy* / drug effects
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Survival Rate

Substances

  • Cytokines
  • Ferrous Compounds
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Interferon-gamma
  • Azoxymethane