How neutrophils kill microbes.
By A. Segal. Annual Review of Immunology, 2005
1,824 citations recorded by the source corpus.
Subfields: Endocrinology, Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/df44e4344bf3f05ca3d114f9f5d2c5a00ae669b8
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In Endocrinology
In Immunology
- Arturo Zychlinsky
- P. Kubes
- V. Brinkmann
- V. Papayannopoulos
- C. Winterbourn
- Kathleen D. Metzler
- A. Mantovani
- M. Hampton
In Molecular Biology
Citations in the corpus
- Reactive Oxygen Species and Neutrophil Function. (2016, background): “The evidence that these involve hydrogen peroxide or superoxide is not particularly strong, and their nature continues to be debated (15, 41, 50, 55, 75, 78).”
- DNase expression allows the pathogen group A Streptococcus to escape killing in neutrophil extracellular traps. (2006, neutral): “Conclusions Neutrophils effectively kill bacteria through a variety of mechanisms involving phagocytosis and/or degranulation, including proteolytic enzymes, antimicrobial peptides, and reactive oxygen and nitrogen species [8].”
- Metabolic Regulation of Immune Responses (2014, background): “Upon pathogen sensing, the latent cytosolic NADPH oxidase complex (NOX) becomes activated in these cells, allowing for generation of the microbicidal H2O2 (13) (Figure 2).”
- How human neutrophils kill and degrade microbes: an integrated view (2007, background): “As a consequence of the resultant high intraphagosomal [Kþ], granule proteases are released from their inactive state complexed with proteoglycans and made available for anti-microbial action (99).”
- The hypersensitive response; the centenary is upon us but how much do we know? (2008, background): “Further, initiation of cell death in the lsd1 mutant was influenced by glutathione levels, if not by redox status (Senda and Ogawa, 2004).”
- NOX2 controls phagosomal pH to regulate antigen processing during crosspresentation by dendritic cells. (2006, background): “Very rapidly, however, ROS production stops, phagosome acidification resumes, and the pH drops within 30 min of phagocytosis (Segal, 2005; Segal et al., 1981).”
- Neutrophil Elastase, Proteinase 3, and Cathepsin G as Therapeutic Targets in Human Diseases (2010, neutral): “oxygen metabolites (Segal, 2005).”
- Myeloperoxidase: a front‐line defender against phagocytosed microorganisms (2013, background): “also been proposed [3], although subsequently challenged [4,”
- PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps (2010, background): “Vol. 207 No. 9 1853-1862 www.jem.org/cgi/doi/10.1084/jem.20100239 1853 Br ief Definit ive Repor t Peripheral blood neutrophils are the first line of defense after bacterial infection (Segal, 2005; Nathan, 2006).”
- Regulation of reactive oxygen species generation in cell signaling (2011, background): “The catalytic protein Nox2 serves as the core protein of NADPH oxidase complex in phagocytic cells (Segal, 2005).”
- Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood (2007, background): “During localized or less severe bacteremia, the platelet is not activated and neutrophils use the more classical Fc and complement receptors to grab and phagocytose bacteri”
- Neutrophils in the activation and regulation of innate and adaptive immunity (2011, background): “A comprehensive overview of the functions of neutrophils in the innate immune system is beyond the scope of this section and the reader is referred to previous reviews for a backgroun”
- Combating oxidative stress in vascular disease: NADPH oxidases as therapeutic targets (2011, background): “NOX2 oxidase-expressing leukocytes classically comprise cells of the innate immune system — that is, neutrophils, monocytes and macrophage”
- Novel cell death program leads to neutrophil extracellular traps (2007, positive): “These data further support our fi nding that NADPH oxidase is essential not only for phagosomal killing (Fang, 2004; Segal, 2005) but also for NET formation.”