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Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components
The colonial ascidian Botryllus schlosseri expresses a unique allorecognition system. When two histoincompatible Botryllus colonies come into direct contact, they develop an inflammatory-like rejection response. A surprising high number of vertebrates' coagulation genes and coagulation-related...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527998/ https://www.ncbi.nlm.nih.gov/pubmed/18769590 http://dx.doi.org/10.1371/journal.pone.0003123 |
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author | Oren, Matan Escande, Marie-line Paz, Guy Fishelson, Zvi Rinkevich, Baruch |
author_facet | Oren, Matan Escande, Marie-line Paz, Guy Fishelson, Zvi Rinkevich, Baruch |
author_sort | Oren, Matan |
collection | PubMed |
description | The colonial ascidian Botryllus schlosseri expresses a unique allorecognition system. When two histoincompatible Botryllus colonies come into direct contact, they develop an inflammatory-like rejection response. A surprising high number of vertebrates' coagulation genes and coagulation-related domains were disclosed in a cDNA library of differentially expressed sequence tags (ESTs), prepared for this allorejection process. Serine proteases, especially from the trypsin family, were highly represented among Botryllus library ortholgues and its “molecular function” gene ontology analysis. These, together with the built-up clot-like lesions in the interaction area, led us to further test whether a vertebrate-like clotting system participates in Botryllus innate immunity. Three morphologically distinct clot types (points of rejection; POR) were followed. We demonstrated the specific expression of nine coagulation orthologue transcripts in Botryllus rejection processes and effects of the anti-coagulant heparin on POR formation and heartbeats. In situ hybridization of fibrinogen and von Willebrand factor orthologues elucidated enhanced expression patterns specific to histoincompatible reactions as well as common expressions not augmented by innate immunity. Immunohistochemistry for fibrinogen revealed, in naïve and immune challenged colonies alike, specific antibody binding to a small population of Botryllus compartment cells. Altogether, molecular, physiological and morphological outcomes suggest the involvement of vertebrates-like coagulation elements in urochordate immunity, not assigned with vasculature injury. |
format | Text |
id | pubmed-2527998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25279982008-09-03 Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components Oren, Matan Escande, Marie-line Paz, Guy Fishelson, Zvi Rinkevich, Baruch PLoS One Research Article The colonial ascidian Botryllus schlosseri expresses a unique allorecognition system. When two histoincompatible Botryllus colonies come into direct contact, they develop an inflammatory-like rejection response. A surprising high number of vertebrates' coagulation genes and coagulation-related domains were disclosed in a cDNA library of differentially expressed sequence tags (ESTs), prepared for this allorejection process. Serine proteases, especially from the trypsin family, were highly represented among Botryllus library ortholgues and its “molecular function” gene ontology analysis. These, together with the built-up clot-like lesions in the interaction area, led us to further test whether a vertebrate-like clotting system participates in Botryllus innate immunity. Three morphologically distinct clot types (points of rejection; POR) were followed. We demonstrated the specific expression of nine coagulation orthologue transcripts in Botryllus rejection processes and effects of the anti-coagulant heparin on POR formation and heartbeats. In situ hybridization of fibrinogen and von Willebrand factor orthologues elucidated enhanced expression patterns specific to histoincompatible reactions as well as common expressions not augmented by innate immunity. Immunohistochemistry for fibrinogen revealed, in naïve and immune challenged colonies alike, specific antibody binding to a small population of Botryllus compartment cells. Altogether, molecular, physiological and morphological outcomes suggest the involvement of vertebrates-like coagulation elements in urochordate immunity, not assigned with vasculature injury. Public Library of Science 2008-09-01 /pmc/articles/PMC2527998/ /pubmed/18769590 http://dx.doi.org/10.1371/journal.pone.0003123 Text en Oren 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Oren, Matan Escande, Marie-line Paz, Guy Fishelson, Zvi Rinkevich, Baruch Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title | Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title_full | Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title_fullStr | Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title_full_unstemmed | Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title_short | Urochordate Histoincompatible Interactions Activate Vertebrate-Like Coagulation System Components |
title_sort | urochordate histoincompatible interactions activate vertebrate-like coagulation system components |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527998/ https://www.ncbi.nlm.nih.gov/pubmed/18769590 http://dx.doi.org/10.1371/journal.pone.0003123 |
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