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Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization
The M22.8 monoclonal antibody (mAb) developed against an antigen expressed at the mussel larval and postlarval stages of Mytilus galloprovincialis was studied on adult samples. Antigenic characterization by Western blot showed that the antigen MSP22.8 has a restricted distribution that includes mant...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805170/ https://www.ncbi.nlm.nih.gov/pubmed/27008638 http://dx.doi.org/10.1371/journal.pone.0152210 |
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author | Calvo-Iglesias, Juan Pérez-Estévez, Daniel Lorenzo-Abalde, Silvia Sánchez-Correa, Beatriz Quiroga, María Isabel Fuentes, José M. González-Fernández, África |
author_facet | Calvo-Iglesias, Juan Pérez-Estévez, Daniel Lorenzo-Abalde, Silvia Sánchez-Correa, Beatriz Quiroga, María Isabel Fuentes, José M. González-Fernández, África |
author_sort | Calvo-Iglesias, Juan |
collection | PubMed |
description | The M22.8 monoclonal antibody (mAb) developed against an antigen expressed at the mussel larval and postlarval stages of Mytilus galloprovincialis was studied on adult samples. Antigenic characterization by Western blot showed that the antigen MSP22.8 has a restricted distribution that includes mantle edge tissue, extrapallial fluid, extrapallial fluid hemocytes, and the shell organic matrix of adult samples. Other tissues such as central mantle, gonadal tissue, digestive gland, labial palps, foot, and byssal retractor muscle did not express the antigen. Immunohistochemistry assays identified MSP22.8 in cells located in the outer fold epithelium of the mantle edge up to the pallial line. Flow cytometry analysis showed that hemocytes from the extrapallial fluid also contain the antigen intracellularly. Furthermore, hemocytes from hemolymph have the ability to internalize the antigen when exposed to a cell-free extrapallial fluid solution. Our findings indicate that hemocytes could play an important role in the biomineralization process and, as a consequence, they have been included in a model of shell formation. This is the first report concerning a protein secreted by the mantle edge into the extrapallial space and how it becomes part of the shell matrix framework in M. galloprovincialis mussels. |
format | Online Article Text |
id | pubmed-4805170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48051702016-03-25 Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization Calvo-Iglesias, Juan Pérez-Estévez, Daniel Lorenzo-Abalde, Silvia Sánchez-Correa, Beatriz Quiroga, María Isabel Fuentes, José M. González-Fernández, África PLoS One Research Article The M22.8 monoclonal antibody (mAb) developed against an antigen expressed at the mussel larval and postlarval stages of Mytilus galloprovincialis was studied on adult samples. Antigenic characterization by Western blot showed that the antigen MSP22.8 has a restricted distribution that includes mantle edge tissue, extrapallial fluid, extrapallial fluid hemocytes, and the shell organic matrix of adult samples. Other tissues such as central mantle, gonadal tissue, digestive gland, labial palps, foot, and byssal retractor muscle did not express the antigen. Immunohistochemistry assays identified MSP22.8 in cells located in the outer fold epithelium of the mantle edge up to the pallial line. Flow cytometry analysis showed that hemocytes from the extrapallial fluid also contain the antigen intracellularly. Furthermore, hemocytes from hemolymph have the ability to internalize the antigen when exposed to a cell-free extrapallial fluid solution. Our findings indicate that hemocytes could play an important role in the biomineralization process and, as a consequence, they have been included in a model of shell formation. This is the first report concerning a protein secreted by the mantle edge into the extrapallial space and how it becomes part of the shell matrix framework in M. galloprovincialis mussels. Public Library of Science 2016-03-23 /pmc/articles/PMC4805170/ /pubmed/27008638 http://dx.doi.org/10.1371/journal.pone.0152210 Text en © 2016 Calvo-Iglesias et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Calvo-Iglesias, Juan Pérez-Estévez, Daniel Lorenzo-Abalde, Silvia Sánchez-Correa, Beatriz Quiroga, María Isabel Fuentes, José M. González-Fernández, África Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title | Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title_full | Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title_fullStr | Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title_full_unstemmed | Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title_short | Characterization of a Monoclonal Antibody Directed against Mytilus spp Larvae Reveals an Antigen Involved in Shell Biomineralization |
title_sort | characterization of a monoclonal antibody directed against mytilus spp larvae reveals an antigen involved in shell biomineralization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805170/ https://www.ncbi.nlm.nih.gov/pubmed/27008638 http://dx.doi.org/10.1371/journal.pone.0152210 |
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