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

Author:

Romao Susana1,Gasser Nathalie1,Becker Andrea C.2,Guhl Bruno1,Bajagic Milica1,Vanoaica Danusia1,Ziegler Urs1,Roesler Joachim3,Dengjel Jörn22,Reichenbach Janine4,Münz Christian1

Affiliation:

1. Viral Immunobiology, Institute of Experimental Immunology, and Center for Microscopy and Image Analysis, University of Zürich, 8006 Zürich, Switzerland

2. School of Life Sciences–LifeNet, Freiburg Institute for Advanced Studies, and Centre for Biological Signalling Studies, University of Freiburg, 79085 Freiburg, Germany

3. Department of Pediatrics, University Clinic Carl Gustav Carus Dresden, 01307 Dresden, Germany

4. Division of Immunology/Hematology/Bone Marrow Transplantation, Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies and Children’s Research Center, University Children’s Hospital Zürich, 8032 Zürich, Switzerland

Abstract

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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