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Was the evolutionary road towards adaptive immunity paved with endothelium?
BACKGROUND: The characterization of a completely novel adaptive immune system (AIS) in jawless vertebrates (hagfish and lampreys) presents an excellent opportunity for exploring similarities and differences in design principles. It also highlights a somewhat neglected question: Why did vertebrates,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560925/ https://www.ncbi.nlm.nih.gov/pubmed/26341882 http://dx.doi.org/10.1186/s13062-015-0079-0 |
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author | van Niekerk, Gustav Davis, Tanja Engelbrecht, Anna-Mart |
author_facet | van Niekerk, Gustav Davis, Tanja Engelbrecht, Anna-Mart |
author_sort | van Niekerk, Gustav |
collection | PubMed |
description | BACKGROUND: The characterization of a completely novel adaptive immune system (AIS) in jawless vertebrates (hagfish and lampreys) presents an excellent opportunity for exploring similarities and differences in design principles. It also highlights a somewhat neglected question: Why did vertebrates, representing only 5 % of all animals, evolve a system as complex as an AIS twice, whereas invertebrates failed to do so? A number of theories have been presented in answer to this question. However, these theories either fail to explain why invertebrates would not similarly develop an AIS and are confounded by issues of causality, or have been challenged by more recent findings. PRESENTATION OF THE HYPOTHESIS: Instead of identifying a selective pressure that would drive the development of an AIS, we hypothesise that invertebrates failed to develop an AIS because of the evolutionary constraints imposed by these animals’ physiological context. In particular, we argue that a number of vascular innovations in vertebrates allowed the effective implementation of an AIS. A lower blood volume allowed for a higher antibody titer (i.e., less ‘diluted’ antibody concentration), rendering these immune effectors more cost-effective. In addition, both a high circulatory velocity and the ability of endothelium to coordinate immune cell trafficking promote ‘epitope sampling’. Collectively, these innovations allowed the effective implementation of AIS in vertebrates. TESTING THE HYPOTHESIS: The hypothesis posits that a number of innovations to the vascular system provided the release from constraints which allowed the implementation of an AIS. However, this hypothesis would be refuted by phylogenetic analysis demonstrating that the AIS preceded these vascular innovations. The hypothesis also suggests that vascular performance would have an impact on the efficacy of an AIS, thus predicting a correlation between the vascular parameters of a species and its relative investment in AIS. The contribution of certain vascular innovations in augmenting immune functionality of an AIS can be tested by modelling the effect of different vascular parameters on AIS efficacy. IMPLICATIONS OF THE HYPOTHESIS: The hypothesis not only explains the immunological dimorphism between vertebrates and invertebrates but also brings to attention the fact that immunity is dependent on more than just an immune system. REVIEWERS: This article was reviewed by Dr. Jun Yu and Prof. Neil Greenspan. |
format | Online Article Text |
id | pubmed-4560925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45609252015-09-06 Was the evolutionary road towards adaptive immunity paved with endothelium? van Niekerk, Gustav Davis, Tanja Engelbrecht, Anna-Mart Biol Direct Hypothesis BACKGROUND: The characterization of a completely novel adaptive immune system (AIS) in jawless vertebrates (hagfish and lampreys) presents an excellent opportunity for exploring similarities and differences in design principles. It also highlights a somewhat neglected question: Why did vertebrates, representing only 5 % of all animals, evolve a system as complex as an AIS twice, whereas invertebrates failed to do so? A number of theories have been presented in answer to this question. However, these theories either fail to explain why invertebrates would not similarly develop an AIS and are confounded by issues of causality, or have been challenged by more recent findings. PRESENTATION OF THE HYPOTHESIS: Instead of identifying a selective pressure that would drive the development of an AIS, we hypothesise that invertebrates failed to develop an AIS because of the evolutionary constraints imposed by these animals’ physiological context. In particular, we argue that a number of vascular innovations in vertebrates allowed the effective implementation of an AIS. A lower blood volume allowed for a higher antibody titer (i.e., less ‘diluted’ antibody concentration), rendering these immune effectors more cost-effective. In addition, both a high circulatory velocity and the ability of endothelium to coordinate immune cell trafficking promote ‘epitope sampling’. Collectively, these innovations allowed the effective implementation of AIS in vertebrates. TESTING THE HYPOTHESIS: The hypothesis posits that a number of innovations to the vascular system provided the release from constraints which allowed the implementation of an AIS. However, this hypothesis would be refuted by phylogenetic analysis demonstrating that the AIS preceded these vascular innovations. The hypothesis also suggests that vascular performance would have an impact on the efficacy of an AIS, thus predicting a correlation between the vascular parameters of a species and its relative investment in AIS. The contribution of certain vascular innovations in augmenting immune functionality of an AIS can be tested by modelling the effect of different vascular parameters on AIS efficacy. IMPLICATIONS OF THE HYPOTHESIS: The hypothesis not only explains the immunological dimorphism between vertebrates and invertebrates but also brings to attention the fact that immunity is dependent on more than just an immune system. REVIEWERS: This article was reviewed by Dr. Jun Yu and Prof. Neil Greenspan. BioMed Central 2015-09-04 /pmc/articles/PMC4560925/ /pubmed/26341882 http://dx.doi.org/10.1186/s13062-015-0079-0 Text en © van Niekerk et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Hypothesis van Niekerk, Gustav Davis, Tanja Engelbrecht, Anna-Mart Was the evolutionary road towards adaptive immunity paved with endothelium? |
title | Was the evolutionary road towards adaptive immunity paved with endothelium? |
title_full | Was the evolutionary road towards adaptive immunity paved with endothelium? |
title_fullStr | Was the evolutionary road towards adaptive immunity paved with endothelium? |
title_full_unstemmed | Was the evolutionary road towards adaptive immunity paved with endothelium? |
title_short | Was the evolutionary road towards adaptive immunity paved with endothelium? |
title_sort | was the evolutionary road towards adaptive immunity paved with endothelium? |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560925/ https://www.ncbi.nlm.nih.gov/pubmed/26341882 http://dx.doi.org/10.1186/s13062-015-0079-0 |
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