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本文引用的文献

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The Biology and Underlying Mechanisms of Cross-Presentation of Exogenous Antigens on MHC-I Molecules.外源性抗原在MHC-I分子上的交叉呈递的生物学及潜在机制
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Autophagy Beyond Intracellular MHC Class II Antigen Presentation.自噬不仅仅局限于细胞内 MHC Ⅱ类抗原递呈。
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Normalizing Microbiota-Induced Retinoic Acid Deficiency Stimulates Protective CD8(+) T Cell-Mediated Immunity in Colorectal Cancer.使微生物群诱导的视黄酸缺乏正常化可刺激结直肠癌中具有保护作用的CD8(+) T细胞介导的免疫。
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Combined deletion of cathepsin protease family members reveals compensatory mechanisms in cancer.组织蛋白酶蛋白酶家族成员的联合缺失揭示了癌症中的代偿机制。
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Cancer statistics, 2016.癌症统计数据,2016 年。
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Antigen Presentation by MHC-Dressed Cells.由MHC修饰的细胞进行抗原呈递。
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8
Redirecting soluble antigen for MHC class I cross-presentation during phagocytosis.在吞噬作用过程中重定向可溶性抗原以进行MHC I类交叉提呈。
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10
Out-of-frame start codons prevent translation of truncated nucleo-cytosolic cathepsin L in vivo.框架外起始密码子阻止核质胞浆组织蛋白酶 L 的截断翻译。
Nat Commun. 2014 Sep 15;5:4931. doi: 10.1038/ncomms5931.

肠上皮细胞中的自噬在肿瘤发生过程中触发适应性免疫。

Mitophagy in Intestinal Epithelial Cells Triggers Adaptive Immunity during Tumorigenesis.

机构信息

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.

出版信息

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

DOI:10.1016/j.cell.2018.05.028
PMID:29909986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6354256/
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.

摘要

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。