Autophagy and Reactive Oxygen Species Are Involved in Neutrophil Extracellular Traps Release Induced by C-albicans Morphotypes

被引:71
作者
Kenno, Samyr [1 ]
Perito, Stefano [2 ]
Mosci, Paolo [3 ]
Vecchiarelli, Anna [2 ]
Monari, Claudia [2 ]
机构
[1] Med Univ Innsbruck, Div Hyg & Med Microbiol, A-6020 Innsbruck, Austria
[2] Univ Perugia, Dept Expt Med, Microbiol Sect, I-06100 Perugia, Italy
[3] Univ Perugia, Dept Vet Med, Internal Med, I-06100 Perugia, Italy
关键词
NET; autophagy; ROS; C; albicans; neutrophils; CRYPTOCOCCUS-NEOFORMANS; MECHANISM; SURVIVAL; IMMUNITY; MODULATION; INHIBITORS; INFECTION;
D O I
10.3389/fmicb.2016.00879
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Neutrophil extracellular traps (NETs) are a combination of DNA fibers and granular enzymes, such as elastase and myeloperoxidase. In this study, we demonstrate that Candida albicans hyphal (CAH) cells and yeast (CAY) cells induce differential amounts, kinetics and mechanisms of NET release. CAH cells induced larger quantities of NET compared to CAY cells and can stimulate rapid NET formation up to 4 h of incubation. CAY cells are, also, able to induce rapid NET formation, but this ability was lost at 4 h. Both reactive oxygen species (ROS) and autophagy are implicated in NET induced by CAH and CAY cells, but with a time-different participation of these two mechanisms. In particular, in the early phase (15 min) CAH cells stimulate NET via autophagy, but not via ROS, while CAY cells induce NET via both autophagy and ROS. At 4 h, only CAH cells stimulate NET formation using autophagy as well as ROS. Finally, we demonstrate that NET release, in response to CAH cells, involves NE-B-k activation and is strongly implicated in hyphal destruction.
引用
收藏
页数:14
相关论文
共 51 条
[11]  
Chen Y, 2012, METHODS MOL BIOL, V844, P115, DOI 10.1007/978-1-61779-527-5_8
[12]   Interplay between Candida albicans and the Mammalian Innate Host Defense [J].
Cheng, Shih-Chin ;
Joosten, Leo A. B. ;
Kullberg, Bart-Jan ;
Netea, Mihai G. .
INFECTION AND IMMUNITY, 2012, 80 (04) :1304-1313
[13]   Bacterial manipulation of innate immunity to promote infection [J].
Diacovich, Lautaro ;
Gorvel, Jean-Pierre .
NATURE REVIEWS MICROBIOLOGY, 2010, 8 (02) :117-128
[14]   A Multifunctional, Synthetic Gaussia princeps Luciferase Reporter for Live Imaging of Candida albicans Infections [J].
Enjalbert, Brice ;
Rachini, Anna ;
Vediyappan, Govindsamy ;
Pietrella, Donatella ;
Spaccapelo, Roberta ;
Vecchiarelli, Anna ;
Brown, Alistair J. P. ;
d'Enfert, Christophe .
INFECTION AND IMMUNITY, 2009, 77 (11) :4847-4858
[15]   Candida albicans escapes from mouse neutrophils [J].
Ermert, David ;
Niemiec, Maria J. ;
Rohm, Marc ;
Glenthoj, Andreas ;
Borregaard, Niels ;
Urban, Constantin F. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2013, 94 (02) :223-236
[16]   Mouse Neutrophil Extracellular Traps in Microbial Infections [J].
Ermert, David ;
Urban, Constantin F. ;
Laube, Britta ;
Goosmann, Christian ;
Zychlinsky, Arturo ;
Brinkmann, Volker .
JOURNAL OF INNATE IMMUNITY, 2009, 1 (03) :181-193
[17]   Novel cell death program leads to neutrophil extracellular traps [J].
Fuchs, Tobias A. ;
Abed, Ulrike ;
Goosmann, Christian ;
Hurwitz, Robert ;
Schulze, Ilka ;
Wahn, Volker ;
Weinrauch, Yvette ;
Brinkmann, Volker ;
Zychlinsky, Arturo .
JOURNAL OF CELL BIOLOGY, 2007, 176 (02) :231-241
[18]   Role of phosphatidylinositol-3-kinase (PI3K), extracellular signal-regulated kinase (ERK) and nuclear transcription factor kappa β (NF-kβ) on neutrophil phagocytic process of Candida albicans [J].
Giraldo, E. ;
Martin-Cordero, L. ;
Hinchado, M. D. ;
Garcia, J. J. ;
Ortega, E. .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2010, 333 (1-2) :115-120
[19]   Candida albicans switches mates [J].
Gow, NAR .
MOLECULAR CELL, 2002, 10 (02) :217-218
[20]   Autophagy is a defense mechanism inhibiting BCG and Mycobacterium tuberculosis survival in infected macrophages [J].
Gutierrez, MG ;
Master, SS ;
Singh, SB ;
Taylor, GA ;
Colombo, MI ;
Deretic, V .
CELL, 2004, 119 (06) :753-766