NETosis markers: Quest for specific, objective, and quantitative markers
More than 10years have passed since the discovery of neutrophil extracellular traps (NETs) in 2004. NETs are extracellular web-like DNA decorated with antimicrobial proteins, which are released from activated neutrophils. The state of neutrophils with NET formation is called NETosis. It has been rea...
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Veröffentlicht in: | Clinica chimica acta 2016-08, Vol.459, p.89-93 |
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description | More than 10years have passed since the discovery of neutrophil extracellular traps (NETs) in 2004. NETs are extracellular web-like DNA decorated with antimicrobial proteins, which are released from activated neutrophils. The state of neutrophils with NET formation is called NETosis. It has been realized that NETosis includes suicidal NETosis and vital NETosis. The former state means cell death of neutrophils, whereas the latter state preserves living neutrophilic functions. Although both suicidal and vital NETosis play essential roles in elimination of microorganisms, excessive formation of NETs, especially the ones derived from suicidal NETosis, can harm the hosts. Therefore, the discovery of NETosis markers and development of evaluation methods are important. In this review, we compare the methods for evaluating NETosis, including immunocytological and immunohistological detection of co-localized neutrophil-derived proteins and extracellular DNA, and citrullinated histones, detection of NET remnants in fluid samples, and flow cytometric detection of cell-appendant NET components, with focus on the specificity, objectivity, and quantitativity. Since the gold standard marker of NETosis or method of NET detection has not been established yet, researchers should choose the most appropriate marker or method in each situation based on the knowledge of the respective virtues and faults.
•Many studies have been conducted to evaluate NETosis in vitro and in vivo.•These include immunological and flow cytometric detection of NET components and assay for NET remnants in fluid samples.•We compare the methods for evaluating NETosis with focus on the specificity, objectivity, and quantitativity. |
doi_str_mv | 10.1016/j.cca.2016.05.029 |
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•Many studies have been conducted to evaluate NETosis in vitro and in vivo.•These include immunological and flow cytometric detection of NET components and assay for NET remnants in fluid samples.•We compare the methods for evaluating NETosis with focus on the specificity, objectivity, and quantitativity.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/j.cca.2016.05.029</identifier><identifier>PMID: 27259468</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Biomarkers - analysis ; Citrullinated histone ; Extracellular Traps - chemistry ; Extracellular Traps - immunology ; Flow Cytometry ; Humans ; MPO-DNA complex ; Neutrophil extracellular trap ; Neutrophils - chemistry ; Neutrophils - immunology ; Peptidylarginine deiminase 4</subject><ispartof>Clinica chimica acta, 2016-08, Vol.459, p.89-93</ispartof><rights>2016 The Authors</rights><rights>Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-8cd9d189cb9a63fb1481ff992fb639230be7802b5845935204d646806f0525f13</citedby><cites>FETCH-LOGICAL-c506t-8cd9d189cb9a63fb1481ff992fb639230be7802b5845935204d646806f0525f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S000989811630242X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27259468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masuda, Sakiko</creatorcontrib><creatorcontrib>Nakazawa, Daigo</creatorcontrib><creatorcontrib>Shida, Haruki</creatorcontrib><creatorcontrib>Miyoshi, Arina</creatorcontrib><creatorcontrib>Kusunoki, Yoshihiro</creatorcontrib><creatorcontrib>Tomaru, Utano</creatorcontrib><creatorcontrib>Ishizu, Akihiro</creatorcontrib><title>NETosis markers: Quest for specific, objective, and quantitative markers</title><title>Clinica chimica acta</title><addtitle>Clin Chim Acta</addtitle><description>More than 10years have passed since the discovery of neutrophil extracellular traps (NETs) in 2004. NETs are extracellular web-like DNA decorated with antimicrobial proteins, which are released from activated neutrophils. The state of neutrophils with NET formation is called NETosis. It has been realized that NETosis includes suicidal NETosis and vital NETosis. The former state means cell death of neutrophils, whereas the latter state preserves living neutrophilic functions. Although both suicidal and vital NETosis play essential roles in elimination of microorganisms, excessive formation of NETs, especially the ones derived from suicidal NETosis, can harm the hosts. Therefore, the discovery of NETosis markers and development of evaluation methods are important. In this review, we compare the methods for evaluating NETosis, including immunocytological and immunohistological detection of co-localized neutrophil-derived proteins and extracellular DNA, and citrullinated histones, detection of NET remnants in fluid samples, and flow cytometric detection of cell-appendant NET components, with focus on the specificity, objectivity, and quantitativity. Since the gold standard marker of NETosis or method of NET detection has not been established yet, researchers should choose the most appropriate marker or method in each situation based on the knowledge of the respective virtues and faults.
•Many studies have been conducted to evaluate NETosis in vitro and in vivo.•These include immunological and flow cytometric detection of NET components and assay for NET remnants in fluid samples.•We compare the methods for evaluating NETosis with focus on the specificity, objectivity, and quantitativity.</description><subject>Biomarkers - analysis</subject><subject>Citrullinated histone</subject><subject>Extracellular Traps - chemistry</subject><subject>Extracellular Traps - immunology</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>MPO-DNA complex</subject><subject>Neutrophil extracellular trap</subject><subject>Neutrophils - chemistry</subject><subject>Neutrophils - immunology</subject><subject>Peptidylarginine deiminase 4</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kFFLwzAUhYMobk5_gC_SRx_WepMmWaJPMqYThiLM59CmCWRu7Za0A_-9Kdt89OnmhnMO534I3WLIMGD-sMq0LjISnxmwDIg8Q0MsJnmaU0nO0RAAZCqkwAN0FcIqrhQ4vkQDMiFMUi6GaP4-WzbBhWRT-G_jw2Py2ZnQJrbxSdga7azT46QpV0a3bm_GSVFXya4r6ta1Rf9zMl6jC1usg7k5zhH6epktp_N08fH6Nn1epJoBb1OhK1lhIXUpC57bElOBrZWS2JLnkuRQmokAUjJBmcwZAVrxWBS4BUaYxfkI3R9yt77Z9VXVxgVt1uuiNk0XFBaQU0YJ51GKD1LtmxC8sWrrXaz7ozCoHqBaqQhQ9QAVMBUBRs_dMb4rN6b6c5yIRcHTQWDikXtnvAramVqbyvnISFWN-yf-F6xZfwQ</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Masuda, Sakiko</creator><creator>Nakazawa, Daigo</creator><creator>Shida, Haruki</creator><creator>Miyoshi, Arina</creator><creator>Kusunoki, Yoshihiro</creator><creator>Tomaru, Utano</creator><creator>Ishizu, Akihiro</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160801</creationdate><title>NETosis markers: Quest for specific, objective, and quantitative markers</title><author>Masuda, Sakiko ; Nakazawa, Daigo ; Shida, Haruki ; Miyoshi, Arina ; Kusunoki, Yoshihiro ; Tomaru, Utano ; Ishizu, Akihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-8cd9d189cb9a63fb1481ff992fb639230be7802b5845935204d646806f0525f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biomarkers - analysis</topic><topic>Citrullinated histone</topic><topic>Extracellular Traps - chemistry</topic><topic>Extracellular Traps - immunology</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>MPO-DNA complex</topic><topic>Neutrophil extracellular trap</topic><topic>Neutrophils - chemistry</topic><topic>Neutrophils - immunology</topic><topic>Peptidylarginine deiminase 4</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masuda, Sakiko</creatorcontrib><creatorcontrib>Nakazawa, Daigo</creatorcontrib><creatorcontrib>Shida, Haruki</creatorcontrib><creatorcontrib>Miyoshi, Arina</creatorcontrib><creatorcontrib>Kusunoki, Yoshihiro</creatorcontrib><creatorcontrib>Tomaru, Utano</creatorcontrib><creatorcontrib>Ishizu, Akihiro</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masuda, Sakiko</au><au>Nakazawa, Daigo</au><au>Shida, Haruki</au><au>Miyoshi, Arina</au><au>Kusunoki, Yoshihiro</au><au>Tomaru, Utano</au><au>Ishizu, Akihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NETosis markers: Quest for specific, objective, and quantitative markers</atitle><jtitle>Clinica chimica acta</jtitle><addtitle>Clin Chim Acta</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>459</volume><spage>89</spage><epage>93</epage><pages>89-93</pages><issn>0009-8981</issn><eissn>1873-3492</eissn><abstract>More than 10years have passed since the discovery of neutrophil extracellular traps (NETs) in 2004. NETs are extracellular web-like DNA decorated with antimicrobial proteins, which are released from activated neutrophils. The state of neutrophils with NET formation is called NETosis. It has been realized that NETosis includes suicidal NETosis and vital NETosis. The former state means cell death of neutrophils, whereas the latter state preserves living neutrophilic functions. Although both suicidal and vital NETosis play essential roles in elimination of microorganisms, excessive formation of NETs, especially the ones derived from suicidal NETosis, can harm the hosts. Therefore, the discovery of NETosis markers and development of evaluation methods are important. In this review, we compare the methods for evaluating NETosis, including immunocytological and immunohistological detection of co-localized neutrophil-derived proteins and extracellular DNA, and citrullinated histones, detection of NET remnants in fluid samples, and flow cytometric detection of cell-appendant NET components, with focus on the specificity, objectivity, and quantitativity. Since the gold standard marker of NETosis or method of NET detection has not been established yet, researchers should choose the most appropriate marker or method in each situation based on the knowledge of the respective virtues and faults.
•Many studies have been conducted to evaluate NETosis in vitro and in vivo.•These include immunological and flow cytometric detection of NET components and assay for NET remnants in fluid samples.•We compare the methods for evaluating NETosis with focus on the specificity, objectivity, and quantitativity.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27259468</pmid><doi>10.1016/j.cca.2016.05.029</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers - analysis Citrullinated histone Extracellular Traps - chemistry Extracellular Traps - immunology Flow Cytometry Humans MPO-DNA complex Neutrophil extracellular trap Neutrophils - chemistry Neutrophils - immunology Peptidylarginine deiminase 4 |
title | NETosis markers: Quest for specific, objective, and quantitative markers |
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