Autophagy proteins stabilize pathogen-containing phagosomes for prolonged MHC II antigen processing

被引:156
作者
Romao, Susana [1 ]
Gasser, Nathalie [1 ]
Becker, Andrea C. [3 ]
Guhl, Bruno [2 ]
Bajagic, Milica [1 ]
Vanoaica, Danusia [1 ]
Ziegler, Urs [2 ]
Roesler, Joachim [5 ]
Dengjel, Joern [3 ,4 ]
Reichenbach, Janine [6 ,7 ]
Muenz, Christian [1 ]
机构
[1] Univ Zurich, Inst Expt Immunol, CH-8006 Zurich, Switzerland
[2] Univ Zurich, Ctr Microscopy & Image Anal, CH-8006 Zurich, Switzerland
[3] Univ Freiburg, Freiburg Inst Adv Studies, Sch Life Sci Life Net, D-79085 Freiburg, Germany
[4] Univ Freiburg, Ctr Biol Signalling Studies, D-79085 Freiburg, Germany
[5] Univ Clin Carl Gustav Carus Dresden, Dept Pediat, D-01307 Dresden, Germany
[6] Univ Childrens Hosp Zurich, Div Immunol Hematol Bone Marrow Transplantat, Jeffrey Modell Diagnost & Res Ctr Primary Immunod, CH-8032 Zurich, Switzerland
[7] Univ Childrens Hosp Zurich, Childrens Res Ctr, CH-8032 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
MATURATION; PH;
D O I
10.1083/jcb.201308173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antigen preservation for presentation is a hallmark of potent antigen-presenting cells. In this paper, we report that in human macrophages and dendritic cells, a subset of phagosomes gets coated with Atg8/LC3, a component of the molecular machinery of macroautophagy, and maintains phagocytosed antigens for prolonged presentation on major histocompatibility complex class II molecules. These Atg8/LC3-positive phagosomes are formed around the antigen with TLR2 agonists and require reactive oxygen species production by NOX2 for their generation. A deficiency in the NOX2-dependent formation of these antigen storage phagosomes could contribute to compromise antifungal immune control in chronic granulomatous disease patients.
引用
收藏
页码:757 / 766
页数:10
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