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Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity
Understanding the mechanisms that sustain immunological nonreactivity is essential for maintaining tissue in syngeneic and allogeneic settings, such as transplantation and pregnancy tolerance. While most transplantation rejections occur due to the adaptive immune response, the proinflammatory respon...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398012/ https://www.ncbi.nlm.nih.gov/pubmed/34436293 http://dx.doi.org/10.3390/md19080454 |
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author | Goldstein, Oron Mandujano-Tinoco, Edna Ayerim Levy, Tom Talice, Shani Raveh, Tal Gershoni-Yahalom, Orly Voskoboynik, Ayelet Rosental, Benyamin |
author_facet | Goldstein, Oron Mandujano-Tinoco, Edna Ayerim Levy, Tom Talice, Shani Raveh, Tal Gershoni-Yahalom, Orly Voskoboynik, Ayelet Rosental, Benyamin |
author_sort | Goldstein, Oron |
collection | PubMed |
description | Understanding the mechanisms that sustain immunological nonreactivity is essential for maintaining tissue in syngeneic and allogeneic settings, such as transplantation and pregnancy tolerance. While most transplantation rejections occur due to the adaptive immune response, the proinflammatory response of innate immunity is necessary for the activation of adaptive immunity. Botryllus schlosseri, a colonial tunicate, which is the nearest invertebrate group to the vertebrates, is devoid of T- and B-cell-based adaptive immunity. It has unique characteristics that make it a valuable model system for studying innate immunity mechanisms: (i) a natural allogeneic transplantation phenomenon that results in either fusion or rejection; (ii) whole animal regeneration and noninflammatory resorption on a weekly basis; (iii) allogeneic resorption which is comparable to human chronic rejection. Recent studies in B. schlosseri have led to the recognition of a molecular and cellular framework underlying the innate immunity loss of tolerance to allogeneic tissues. Additionally, B. schlosseri was developed as a model for studying hematopoietic stem cell (HSC) transplantation, and it provides further insights into the similarities between the HSC niches of human and B. schlosseri. In this review, we discuss why studying the molecular and cellular pathways that direct successful innate immune tolerance in B. schlosseri can provide novel insights into and potential modulations of these immune processes in humans. |
format | Online Article Text |
id | pubmed-8398012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83980122021-08-29 Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity Goldstein, Oron Mandujano-Tinoco, Edna Ayerim Levy, Tom Talice, Shani Raveh, Tal Gershoni-Yahalom, Orly Voskoboynik, Ayelet Rosental, Benyamin Mar Drugs Review Understanding the mechanisms that sustain immunological nonreactivity is essential for maintaining tissue in syngeneic and allogeneic settings, such as transplantation and pregnancy tolerance. While most transplantation rejections occur due to the adaptive immune response, the proinflammatory response of innate immunity is necessary for the activation of adaptive immunity. Botryllus schlosseri, a colonial tunicate, which is the nearest invertebrate group to the vertebrates, is devoid of T- and B-cell-based adaptive immunity. It has unique characteristics that make it a valuable model system for studying innate immunity mechanisms: (i) a natural allogeneic transplantation phenomenon that results in either fusion or rejection; (ii) whole animal regeneration and noninflammatory resorption on a weekly basis; (iii) allogeneic resorption which is comparable to human chronic rejection. Recent studies in B. schlosseri have led to the recognition of a molecular and cellular framework underlying the innate immunity loss of tolerance to allogeneic tissues. Additionally, B. schlosseri was developed as a model for studying hematopoietic stem cell (HSC) transplantation, and it provides further insights into the similarities between the HSC niches of human and B. schlosseri. In this review, we discuss why studying the molecular and cellular pathways that direct successful innate immune tolerance in B. schlosseri can provide novel insights into and potential modulations of these immune processes in humans. MDPI 2021-08-09 /pmc/articles/PMC8398012/ /pubmed/34436293 http://dx.doi.org/10.3390/md19080454 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Goldstein, Oron Mandujano-Tinoco, Edna Ayerim Levy, Tom Talice, Shani Raveh, Tal Gershoni-Yahalom, Orly Voskoboynik, Ayelet Rosental, Benyamin Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title | Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title_full | Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title_fullStr | Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title_full_unstemmed | Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title_short | Botryllus schlosseri as a Unique Colonial Chordate Model for the Study and Modulation of Innate Immune Activity |
title_sort | botryllus schlosseri as a unique colonial chordate model for the study and modulation of innate immune activity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398012/ https://www.ncbi.nlm.nih.gov/pubmed/34436293 http://dx.doi.org/10.3390/md19080454 |
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