Institute for Tumor Biology and Experimental Therapy, Georg-Speyer-Haus, 60596 Frankfurt am, Germany; Institute of Pathology, Frankfurt University Hospital, 60590 Frankfurt, Germany.
Institute for Tumor Biology and Experimental Therapy, Georg-Speyer-Haus, 60596 Frankfurt am, Germany.
Cell. 2018 Jun 28;174(1):88-101.e16. doi: 10.1016/j.cell.2018.05.028. Epub 2018 Jun 14.
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.
在结直肠癌患者中,肿瘤中细胞毒性 CD8 T 细胞的高密度与更好的预后相关。我们使用 Stat3 功能丧失方法,在两种依赖 wnt/β-catenin 的散发性肠道肿瘤发生的自发模型中,揭示了控制 CD8 T 细胞适应性免疫反应诱导的复杂的肠上皮细胞(IEC)内过程。IEC 中高水平的细胞自噬导致上皮溶酶体中铁(II)的积累,进而触发溶酶体膜通透性。随后蛋白酶释放到细胞质中,通过树突状细胞的交叉染色,增加 MHC Ⅰ类分子的呈递和 CD8 T 细胞的激活。因此,我们的发现强调了线粒体功能、溶酶体完整性和 MHC Ⅰ类分子在 IEC 中的呈递之间以前未被认识到的联系,并表明触发 IEC 中细胞自噬或诱导溶酶体通透性的治疗方法可能在将结直肠癌的肿瘤免疫平衡转向抗肿瘤免疫方面取得成功。