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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...

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Autores principales: Goldstein, Oron, Mandujano-Tinoco, Edna Ayerim, Levy, Tom, Talice, Shani, Raveh, Tal, Gershoni-Yahalom, Orly, Voskoboynik, Ayelet, Rosental, Benyamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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