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1000 Titel
  • Significance of Mast Cell Formed Extracellular Traps in Microbial Defense
1000 Autor/in
  1. Elieh Ali Komi, Daniel |
  2. Kuebler, Wolfgang |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-05-22
1000 Erschienen in
1000 Quellenangabe
  • 62(1):160-179
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s12016-021-08861-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140557/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Mast cells (MCs) are critically involved in microbial defense by releasing antimicrobial peptides (such as cathelicidin LL-37 and defensins) and phagocytosis of microbes. In past years, it has become evident that in addition MCs may eliminate invading pathogens by ejection of web-like structures of DNA strands embedded with proteins known together as extracellular traps (ETs). Upon stimulation of resting MCs with various microorganisms, their products (including superantigens and toxins), or synthetic chemicals, MCs become activated and enter into a multistage process that includes disintegration of the nuclear membrane, release of chromatin into the cytoplasm, adhesion of cytoplasmic granules on the emerging DNA web, and ejection of the complex into the extracellular space. This so-called ETosis is often associated with cell death of the producing MC, and the type of stimulus potentially determines the ratio of surviving vs. killed MCs. Comparison of different microorganisms with specific elimination characteristics such as S pyogenes (eliminated by MCs only through extracellular mechanisms), S aureus (removed by phagocytosis), fungi, and parasites has revealed important aspects of MC extracellular trap (MCET) biology. Molecular studies identified that the formation of MCET depends on NADPH oxidase-generated reactive oxygen species (ROS). In this review, we summarize the present state-of-the-art on the biological relevance of MCETosis, and its underlying molecular and cellular mechanisms. We also provide an overview over the techniques used to study the structure and function of MCETs, including electron microscopy and fluorescence microscopy using specific monoclonal antibodies (mAbs) to detect MCET-associated proteins such as tryptase and histones, and cell-impermeant DNA dyes for labeling of extracellular DNA. Comparing the type and biofunction of further MCET decorating proteins with ETs produced by other immune cells may help provide a better insight into MCET biology in the pathogenesis of autoimmune and inflammatory disorders as well as microbial defense.
1000 Sacherschließung
lokal Histones/metabolism [MeSH]
lokal LL-37
lokal Mast Cells [MeSH]
lokal Microbial defense
lokal Humans [MeSH]
lokal Extracellular traps
lokal Mast cells
lokal Tryptases/metabolism [MeSH]
lokal ROS
lokal Article
lokal Phagocytosis [MeSH]
lokal Extracellular Traps/metabolism [MeSH]
lokal Tryptase
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-0546-5280|https://orcid.org/0000-0003-4100-2961
1000 Hinweis
  • DeepGreen-ID: 4d80e1ba35a04290b43e8f1a5ef0f016 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Erstellt am 2023-04-27T12:48:29.821+0200
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1000 Zuletzt bearbeitet 2023-10-20T12:23:47.595+0200
1000 Objekt bearb. Fri Oct 20 12:23:47 CEST 2023
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