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Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1)
Collectin-11 (CL-11) is a pattern recognition molecule of the lectin pathway of complement with diverse functions spanning from host defense to embryonic development. CL-11 is found in the circulation in heterocomplexes with the homologous collectin-10 (CL-10). Abnormal CL-11 plasma levels are assoc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172411/ https://www.ncbi.nlm.nih.gov/pubmed/30323815 http://dx.doi.org/10.3389/fimmu.2018.02238 |
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author | Bayarri-Olmos, Rafael Kirketerp-Moller, Nikolaj Pérez-Alós, Laura Skjodt, Karsten Skjoedt, Mikkel-Ole Garred, Peter |
author_facet | Bayarri-Olmos, Rafael Kirketerp-Moller, Nikolaj Pérez-Alós, Laura Skjodt, Karsten Skjoedt, Mikkel-Ole Garred, Peter |
author_sort | Bayarri-Olmos, Rafael |
collection | PubMed |
description | Collectin-11 (CL-11) is a pattern recognition molecule of the lectin pathway of complement with diverse functions spanning from host defense to embryonic development. CL-11 is found in the circulation in heterocomplexes with the homologous collectin-10 (CL-10). Abnormal CL-11 plasma levels are associated with the presence of disseminated intravascular coagulation, urinary schistosomiasis, and congenital disorders. Although there has been a marked development in the characterization of CL-11 there is still a scarcity of clinical tools for its analysis. Thus, we generated monoclonal antibodies and developed a quantitative ELISA to measure CL-11 in the circulation. The antibodies were screened against recombinant CL-11 and validated by ELISA and immunoprecipitation of serum and plasma. The best candidates were pairwise compared to develop a quantitative ELISA. The assay was validated regarding its sensitivity, reproducibility, and dilution linearity, demonstrating a satisfactory variability over a working range of 0.29–18.75 ng/ml. The mean plasma concentration of CL-11 in healthy controls was determined to be 289.4 ng/ml (range 143.2–459.4 ng/ml), highly correlated to the levels of CL/10/11 complexes (r = 0.729). Plasma CL-11 and CL-10/11 co-migrated in size exclusion chromatography as two major complexes of ~400 and >600 kDa. Furthermore, we observed a significant decrease at admission in CL-11 plasma levels in patients admitted to intensive care with systemic inflammatory response syndrome. By using the in-house antibodies and recombinant CL-11, we found that CL-11 can bind to zymosan independently of calcium by a separate site from the carbohydrate-binding region. Finally, we showed that CL-11/MASP-2 complexes trigger C4b deposition on zymosan. In conclusion, we have developed a specific and sensitive ELISA to investigate the ever-expanding roles of CL-11 in health and disease and shown a novel interaction between CL-11 and zymosan. |
format | Online Article Text |
id | pubmed-6172411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61724112018-10-15 Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) Bayarri-Olmos, Rafael Kirketerp-Moller, Nikolaj Pérez-Alós, Laura Skjodt, Karsten Skjoedt, Mikkel-Ole Garred, Peter Front Immunol Immunology Collectin-11 (CL-11) is a pattern recognition molecule of the lectin pathway of complement with diverse functions spanning from host defense to embryonic development. CL-11 is found in the circulation in heterocomplexes with the homologous collectin-10 (CL-10). Abnormal CL-11 plasma levels are associated with the presence of disseminated intravascular coagulation, urinary schistosomiasis, and congenital disorders. Although there has been a marked development in the characterization of CL-11 there is still a scarcity of clinical tools for its analysis. Thus, we generated monoclonal antibodies and developed a quantitative ELISA to measure CL-11 in the circulation. The antibodies were screened against recombinant CL-11 and validated by ELISA and immunoprecipitation of serum and plasma. The best candidates were pairwise compared to develop a quantitative ELISA. The assay was validated regarding its sensitivity, reproducibility, and dilution linearity, demonstrating a satisfactory variability over a working range of 0.29–18.75 ng/ml. The mean plasma concentration of CL-11 in healthy controls was determined to be 289.4 ng/ml (range 143.2–459.4 ng/ml), highly correlated to the levels of CL/10/11 complexes (r = 0.729). Plasma CL-11 and CL-10/11 co-migrated in size exclusion chromatography as two major complexes of ~400 and >600 kDa. Furthermore, we observed a significant decrease at admission in CL-11 plasma levels in patients admitted to intensive care with systemic inflammatory response syndrome. By using the in-house antibodies and recombinant CL-11, we found that CL-11 can bind to zymosan independently of calcium by a separate site from the carbohydrate-binding region. Finally, we showed that CL-11/MASP-2 complexes trigger C4b deposition on zymosan. In conclusion, we have developed a specific and sensitive ELISA to investigate the ever-expanding roles of CL-11 in health and disease and shown a novel interaction between CL-11 and zymosan. Frontiers Media S.A. 2018-09-28 /pmc/articles/PMC6172411/ /pubmed/30323815 http://dx.doi.org/10.3389/fimmu.2018.02238 Text en Copyright © 2018 Bayarri-Olmos, Kirketerp-Moller, Pérez-Alós, Skjodt, Skjoedt and Garred. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Bayarri-Olmos, Rafael Kirketerp-Moller, Nikolaj Pérez-Alós, Laura Skjodt, Karsten Skjoedt, Mikkel-Ole Garred, Peter Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title | Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title_full | Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title_fullStr | Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title_full_unstemmed | Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title_short | Development of a Quantitative Assay for the Characterization of Human Collectin-11 (CL-11, CL-K1) |
title_sort | development of a quantitative assay for the characterization of human collectin-11 (cl-11, cl-k1) |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172411/ https://www.ncbi.nlm.nih.gov/pubmed/30323815 http://dx.doi.org/10.3389/fimmu.2018.02238 |
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