LC3-associated phagocytosis in microbial pathogenesis

被引:35
|
作者
Schille, Stefan [1 ]
Crauwels, Peter [1 ]
Bohn, Rebecca [1 ]
Bagola, Katrin [1 ]
Walther, Paul [3 ]
van Zandbergen, Ger [1 ,2 ]
机构
[1] Paul Ehrlich Inst, Dept Immunol, Paul Ehrlich Str 51-59, D-63225 Langen, Germany
[2] Univ Med Mainz, Inst Immunol, Langenbeckstr 1, D-55131 Mainz, Germany
[3] Ulm Univ, Cent Facil EM, Ulm, Germany
关键词
LC3-associated phagocytosis; Fungi; Bacteria; Parasites; Evasion; BACTERIUM LEGIONELLA-PNEUMOPHILA; LC3 CONJUGATION SYSTEM; LISTERIA-MONOCYTOGENES; BURKHOLDERIA-PSEUDOMALLEI; YERSINIA-PSEUDOTUBERCULOSIS; AUTOPHAGY PROTEINS; TOXOPLASMA-GONDII; MAMMALIAN-CELLS; DISTINCT ROLES; HOST;
D O I
10.1016/j.ijmm.2017.10.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phagocytosis is essential for uptake and elimination of pathogenic microorganisms. Autophagy is a highly conserved mechanism for incorporation of cellular constituents to replenish nutrients by degradation. Recently, parts of the autophagy machinery above all microtubule-associated protein 1 light chain 3 (LC3) were found to be specifically recruited to phagosomal membranes resulting in phagosome-lysosome fusion and efficient degradation of internalized cargo in a process termed LC3-associated phagocytosis (LAP). Many pathogenic bacterial, fungal and parasitic microorganisms reside within LAP-targeted single-membrane phagosomes or vacuoles after infection of host cells. In this minireview we describe the state of knowledge on the interaction of pathogens with LAP or LAP-like pathways and report on various pathogens that have evolved strategies to circumvent degradation in LAP compartments.
引用
收藏
页码:228 / 236
页数:9
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