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本文引用的文献

1
Activating autophagy to potentiate immunogenic chemotherapy and radiation therapy.激活自噬以增强免疫化疗和放疗。
Nat Rev Clin Oncol. 2017 Apr;14(4):247-258. doi: 10.1038/nrclinonc.2016.183. Epub 2016 Nov 15.
2
Targeting natural killer cells in cancer immunotherapy.在癌症免疫疗法中靶向自然杀伤细胞。
Nat Immunol. 2016 Aug 19;17(9):1025-36. doi: 10.1038/ni.3518.
3
Atg5 Is Essential for the Development and Survival of Innate Lymphocytes.自噬相关蛋白5对于固有淋巴细胞的发育和存活至关重要。
Cell Rep. 2016 May 31;15(9):1910-9. doi: 10.1016/j.celrep.2016.04.082. Epub 2016 May 19.
4
Emerging insights into natural killer cells in human peripheral tissues.人体外周组织中自然杀伤细胞的新见解。
Nat Rev Immunol. 2016 Apr 28;16(5):310-20. doi: 10.1038/nri.2016.34.
5
FoxO1-mediated autophagy is required for NK cell development and innate immunity.FoxO1介导的自噬是自然杀伤细胞发育和先天免疫所必需的。
Nat Commun. 2016 Mar 24;7:11023. doi: 10.1038/ncomms11023.
6
Autophagy enforces functional integrity of regulatory T cells by coupling environmental cues and metabolic homeostasis.自噬通过将环境线索与代谢稳态相结合来维持调节性T细胞的功能完整性。
Nat Immunol. 2016 Mar;17(3):277-85. doi: 10.1038/ni.3365. Epub 2016 Jan 25.
7
Natural killer cell memory in infection, inflammation and cancer.自然杀伤细胞记忆在感染、炎症和癌症中的作用。
Nat Rev Immunol. 2016 Feb;16(2):112-23. doi: 10.1038/nri.2015.9. Epub 2016 Jan 25.
8
NK cells and cancer: you can teach innate cells new tricks.自然杀伤细胞与癌症:你可以教先天细胞新招。
Nat Rev Cancer. 2016 Jan;16(1):7-19. doi: 10.1038/nrc.2015.5.
9
Organelle-Specific Initiation of Autophagy.细胞器特异性自噬的起始。
Mol Cell. 2015 Aug 20;59(4):522-39. doi: 10.1016/j.molcel.2015.07.021.
10
BNIP3- and BNIP3L-Mediated Mitophagy Promotes the Generation of Natural Killer Cell Memory.BNIP3和BNIP3L介导的线粒体自噬促进自然杀伤细胞记忆的产生。
Immunity. 2015 Aug 18;43(2):331-42. doi: 10.1016/j.immuni.2015.07.012. Epub 2015 Aug 4.

自噬在自然杀伤细胞发育和功能中的作用。

Involvement of autophagy in NK cell development and function.

作者信息

López-Soto Alejandro, Bravo-San Pedro José Manuel, Kroemer Guido, Galluzzi Lorenzo, Gonzalez Segundo

机构信息

a Departamento de Biología Funcional, Área de Inmunología , Universidad de Oviedo, IUOPA , Oviedo , Asturias , Spain.

b Hospital Universitario Central de Asturias , Oviedo , Asturias , Spain.

出版信息

Autophagy. 2017 Mar 4;13(3):633-636. doi: 10.1080/15548627.2016.1274486. Epub 2017 Jan 19.

DOI:10.1080/15548627.2016.1274486
PMID:28103115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5361597/
Abstract

Natural killer (NK) cells are the prototypical members of the recently identified family of innate lymphoid cells (ILCs). Thanks to their cytotoxic and secretory functions, NK cells play a key role in the immune response to cells experiencing various forms of stress, including viral infection and malignant transformation. Autophagy is a highly conserved network of degradative pathways that participate in the maintenance of cellular and organismal homeostasis as they promote adaptation to adverse microenvironmental conditions. The relevance of autophagy in the development and functionality of cellular components of the adaptive immune system is well established. Conversely, whether autophagy also plays an important role in the biology of ILC populations such as NK cells has long remained elusive. Recent experimental evidence shows that ablating Atg5 (autophagy-related 5, an essential component of the autophagic machinery) in NK cells and other specific ILC populations results in progressive mitochondrial damage, reactive oxygen species (ROS) overgeneration, and regulated cell death, hence interrupting ILC development. Moreover, disrupting the interaction of ATG7 with phosphorylated FOXO1 (forkhead box O1) in the cytosol of immature NK cells prevents autophagic responses that are essential for NK cell maturation. These findings suggest that activating autophagy may support the maturation of NK cells and other ILCs that manifest antiviral and anticancer activity.

摘要

自然杀伤(NK)细胞是最近发现的先天性淋巴细胞(ILC)家族的典型成员。由于其细胞毒性和分泌功能,NK细胞在对经历各种形式应激的细胞(包括病毒感染和恶性转化)的免疫反应中起关键作用。自噬是一个高度保守的降解途径网络,它通过促进对不利微环境条件的适应来参与维持细胞和机体的稳态。自噬在适应性免疫系统细胞成分的发育和功能中的相关性已得到充分证实。相反,自噬是否也在诸如NK细胞等ILC群体的生物学中发挥重要作用长期以来一直难以捉摸。最近的实验证据表明,在NK细胞和其他特定的ILC群体中敲除Atg5(自噬相关5,自噬机制的一个重要组成部分)会导致线粒体逐渐受损、活性氧(ROS)过度产生和程序性细胞死亡,从而中断ILC的发育。此外,破坏未成熟NK细胞胞质中ATG7与磷酸化FOXO1(叉头框O1)的相互作用会阻止对NK细胞成熟至关重要的自噬反应。这些发现表明,激活自噬可能支持NK细胞和其他表现出抗病毒和抗癌活性的ILC的成熟。