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Autophagy in immunity
被引:11
|作者:
Munz, Christian
[1
]
机构:
[1] Univ Zurich, Inst Expt Immunol, Viral Immunobiol, Zurich, Switzerland
来源:
基金:
瑞士国家科学基金会;
关键词:
MHC CLASS-II;
CELLS REQUIRE AUTOPHAGY;
LC3-ASSOCIATED PHAGOCYTOSIS;
CROSS-PRESENTATION;
MYCOBACTERIUM-TUBERCULOSIS;
UNCONVENTIONAL SECRETION;
INNATE;
PROTEINS;
ANTIGEN;
COMPLEX;
D O I:
10.1016/bs.pmbts.2020.03.005
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The molecular machinery of macroautophagy consists of Atg proteins and supports cytoplasmic constituent degradation in lysosomes as its canonical function, phagosome maturation and exocytosis. These different biological processes contribute to cell intrinsic, innate and adaptive immunity. For the respective immune responses, Atg proteins mediate direct pathogen degradation, inflammation restriction, antigen presentation on MHC molecules and survival of memory lymphocyte populations. During adaptive immunity MHC class II presentation of antigens is supported and MHC class I presentation restricted by the macroautophagy machinery. Considering these various functions might allow us to predict the outcome of interventions that manipulate the machinery of Atg proteins as immunotherapies for the benefit of human health.
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页码:67 / 85
页数:19
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