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Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3

BACKGROUND: Nuclear histone proteins are released into the extracellular space during sepsis and act as major mediators of death. However, circulating histone levels have not been precisely quantified. METHODS: We developed a novel enzyme-linked immunosorbent assay (ELISA) for detection of circulati...

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Autores principales: Ito, Takashi, Nakahara, Mayumi, Masuda, Yoshiki, Ono, Sachie, Yamada, Shingo, Ishikura, Hiroyasu, Imaizumi, Hitoshi, Kamikokuryo, Chinatsu, Kakihana, Yasuyuki, Maruyama, Ikuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260889/
https://www.ncbi.nlm.nih.gov/pubmed/30505450
http://dx.doi.org/10.1186/s40560-018-0348-y
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author Ito, Takashi
Nakahara, Mayumi
Masuda, Yoshiki
Ono, Sachie
Yamada, Shingo
Ishikura, Hiroyasu
Imaizumi, Hitoshi
Kamikokuryo, Chinatsu
Kakihana, Yasuyuki
Maruyama, Ikuro
author_facet Ito, Takashi
Nakahara, Mayumi
Masuda, Yoshiki
Ono, Sachie
Yamada, Shingo
Ishikura, Hiroyasu
Imaizumi, Hitoshi
Kamikokuryo, Chinatsu
Kakihana, Yasuyuki
Maruyama, Ikuro
author_sort Ito, Takashi
collection PubMed
description BACKGROUND: Nuclear histone proteins are released into the extracellular space during sepsis and act as major mediators of death. However, circulating histone levels have not been precisely quantified. METHODS: We developed a novel enzyme-linked immunosorbent assay (ELISA) for detection of circulating histone H3 levels and evaluated its performance. Using the ELISA, we measured plasma histone H3 levels in C57BL/6 J mice subjected to cecal ligation and puncture (CLP)-induced sepsis. RESULTS: The newly developed ELISA enabled reproducible measurement of histone H3 levels with a working range up to 250 ng/mL. Using the ELISA, we found that plasma histone H3 levels were elevated in septic mice compared with sham-operated mice (p < 0.01). The elevation of histone H3 levels was abrogated when neutrophils were depleted (p < 0.01). CONCLUSIONS: Our novel ELISA provides reproducible measurements of histone H3 levels. Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner. Further studies are needed to evaluate the clinical utility of histone H3 levels in patients with sepsis.
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spelling pubmed-62608892018-11-30 Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3 Ito, Takashi Nakahara, Mayumi Masuda, Yoshiki Ono, Sachie Yamada, Shingo Ishikura, Hiroyasu Imaizumi, Hitoshi Kamikokuryo, Chinatsu Kakihana, Yasuyuki Maruyama, Ikuro J Intensive Care Research BACKGROUND: Nuclear histone proteins are released into the extracellular space during sepsis and act as major mediators of death. However, circulating histone levels have not been precisely quantified. METHODS: We developed a novel enzyme-linked immunosorbent assay (ELISA) for detection of circulating histone H3 levels and evaluated its performance. Using the ELISA, we measured plasma histone H3 levels in C57BL/6 J mice subjected to cecal ligation and puncture (CLP)-induced sepsis. RESULTS: The newly developed ELISA enabled reproducible measurement of histone H3 levels with a working range up to 250 ng/mL. Using the ELISA, we found that plasma histone H3 levels were elevated in septic mice compared with sham-operated mice (p < 0.01). The elevation of histone H3 levels was abrogated when neutrophils were depleted (p < 0.01). CONCLUSIONS: Our novel ELISA provides reproducible measurements of histone H3 levels. Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner. Further studies are needed to evaluate the clinical utility of histone H3 levels in patients with sepsis. BioMed Central 2018-11-26 /pmc/articles/PMC6260889/ /pubmed/30505450 http://dx.doi.org/10.1186/s40560-018-0348-y Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ito, Takashi
Nakahara, Mayumi
Masuda, Yoshiki
Ono, Sachie
Yamada, Shingo
Ishikura, Hiroyasu
Imaizumi, Hitoshi
Kamikokuryo, Chinatsu
Kakihana, Yasuyuki
Maruyama, Ikuro
Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title_full Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title_fullStr Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title_full_unstemmed Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title_short Circulating histone H3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich ELISA for histone H3
title_sort circulating histone h3 levels are increased in septic mice in a neutrophil-dependent manner: preclinical evaluation of a novel sandwich elisa for histone h3
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260889/
https://www.ncbi.nlm.nih.gov/pubmed/30505450
http://dx.doi.org/10.1186/s40560-018-0348-y
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