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Development of a newly immunoassay specific for mouse presepsin (sCD14-ST)
Presepsin (sCD14-ST) is used as a marker for sepsis diagnosis. The production mechanism of presepsin is unique in that it is produced through phagocytosis of microorganisms. However, some studies have demonstrated that non-infected patients had increased presepsin levels and that presepsin is relate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9755121/ https://www.ncbi.nlm.nih.gov/pubmed/36522357 http://dx.doi.org/10.1038/s41598-022-22096-1 |
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author | Takahashi, Gaku Hoshikawa, Kouichi Suzuki, Rioto Sato, Kotaro Hoshi, Shintaro Yoshinao, Daisuke Shirakawa, Kamon |
author_facet | Takahashi, Gaku Hoshikawa, Kouichi Suzuki, Rioto Sato, Kotaro Hoshi, Shintaro Yoshinao, Daisuke Shirakawa, Kamon |
author_sort | Takahashi, Gaku |
collection | PubMed |
description | Presepsin (sCD14-ST) is used as a marker for sepsis diagnosis. The production mechanism of presepsin is unique in that it is produced through phagocytosis of microorganisms. However, some studies have demonstrated that non-infected patients had increased presepsin levels and that presepsin is related to the risk or severity of diseases. This study was designed to describe a sensitive sandwich enzyme-linked immunosorbent assay for mouse presepsin developed to investigate the association of presepsin with diseases. Polyclonal antibodies were generated from peptide-immunized rabbit antiserum. Mouse presepsin standard was prepared using the recombinant method as an Fc-fusion protein. The linear detection range of the method was 4.7–300 pg/mL with a detection limit of 1.4 pg/mL. The assay detected mouse presepsin where mouse soluble CD14 (sCD14) was digested by cathepsin D proteinase and the cross-reactivity of sCD14 was not observed. The normal levels of mouse presepsin and sCD14 were compared; 65.9 ± 21.4 pg/mL and 43.2 ± 7.2 ng/mL were determined, respectively. Moreover, the levels of presepsin and sCD14 were compared with a lipopolysaccharide (LPS)-injected sepsis mouse model. The newly developed analytical method had high specificity to presepsin and is an efficient tool for studying the association between presepsin and diseases. |
format | Online Article Text |
id | pubmed-9755121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97551212022-12-17 Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) Takahashi, Gaku Hoshikawa, Kouichi Suzuki, Rioto Sato, Kotaro Hoshi, Shintaro Yoshinao, Daisuke Shirakawa, Kamon Sci Rep Article Presepsin (sCD14-ST) is used as a marker for sepsis diagnosis. The production mechanism of presepsin is unique in that it is produced through phagocytosis of microorganisms. However, some studies have demonstrated that non-infected patients had increased presepsin levels and that presepsin is related to the risk or severity of diseases. This study was designed to describe a sensitive sandwich enzyme-linked immunosorbent assay for mouse presepsin developed to investigate the association of presepsin with diseases. Polyclonal antibodies were generated from peptide-immunized rabbit antiserum. Mouse presepsin standard was prepared using the recombinant method as an Fc-fusion protein. The linear detection range of the method was 4.7–300 pg/mL with a detection limit of 1.4 pg/mL. The assay detected mouse presepsin where mouse soluble CD14 (sCD14) was digested by cathepsin D proteinase and the cross-reactivity of sCD14 was not observed. The normal levels of mouse presepsin and sCD14 were compared; 65.9 ± 21.4 pg/mL and 43.2 ± 7.2 ng/mL were determined, respectively. Moreover, the levels of presepsin and sCD14 were compared with a lipopolysaccharide (LPS)-injected sepsis mouse model. The newly developed analytical method had high specificity to presepsin and is an efficient tool for studying the association between presepsin and diseases. Nature Publishing Group UK 2022-12-15 /pmc/articles/PMC9755121/ /pubmed/36522357 http://dx.doi.org/10.1038/s41598-022-22096-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Takahashi, Gaku Hoshikawa, Kouichi Suzuki, Rioto Sato, Kotaro Hoshi, Shintaro Yoshinao, Daisuke Shirakawa, Kamon Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title | Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title_full | Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title_fullStr | Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title_full_unstemmed | Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title_short | Development of a newly immunoassay specific for mouse presepsin (sCD14-ST) |
title_sort | development of a newly immunoassay specific for mouse presepsin (scd14-st) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9755121/ https://www.ncbi.nlm.nih.gov/pubmed/36522357 http://dx.doi.org/10.1038/s41598-022-22096-1 |
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