Literature DB >> 27520114

Listeria monocytogenes induces mast cell extracellular traps.

Marcia Campillo-Navarro1, Kahiry Leyva-Paredes1, Luis Donis-Maturano2, Marco González-Jiménez3, Yuriria Paredes-Vivas3, Arturo Cerbulo-Vázquez4, Jeanet Serafín-López1, Blanca García-Pérez1, Stephen E Ullrich5, Leopoldo Flores-Romo2, Sonia M Pérez-Tapia6, Sergio Estrada-Parra1, Iris Estrada-García1, Rommel Chacón-Salinas7.   

Abstract

Mast cells play an essential role in different immunological phenomena including allergy and infectious diseases. Several bacteria induce mast cell activation leading to degranulation and the production of several cytokines and chemokines. However, mast cells also have different microbicidal activities such as phagocytosis and the release of DNA with embedded granular proteins known as Mast Cell Extracellular Traps (MCETs). Although previous reports indicate that extracellular bacteria are able to induce MCETs little is known if intracellular bacteria can induce these structures. In this work, we evaluated MCETs induction by the intracellular bacteria Listeria monocytogenes. We found that mast cells released DNA after stimulation with L. monocytogenes, and this DNA was complexed to histone and tryptase. Before extracellular DNA release, L. monocytogenes induced modifications to the mast cell nuclear envelope and DNA was detected outside the nucleus. L. monocytogenes stimulated mast cells to produce significant amounts of reactive oxygen species (ROS) and blocking NADPH oxidase diminished DNA release by mast cells. Finally, MCETs showed antimicrobial activity against L. monocytogenes that was partially blocked when β-hexosaminidase activity was inhibited. These results show that L. monocytogenes induces mast cells to produce microbicidal MCETs, suggesting a role for mast cells in containing infection beyond the induction of inflammation.
Copyright © 2016 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Listeria monocytogenes; Mast cell; Mast cell extracellular trap; β-Hexosaminidase

Mesh:

Substances:

Year:  2016        PMID: 27520114     DOI: 10.1016/j.imbio.2016.08.006

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


  20 in total

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