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The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells

T lymphocytes are key cellular components of the adaptive immune system and play a central role in cell-mediated immunity in vertebrates. Despite their heterogeneities, it is believed that all different types of T lymphocytes are generated exclusively via the differentiation of hematopoietic stem ce...

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Autores principales: Tian, Ye, Xu, Jin, Feng, Shachuan, He, Sicong, Zhao, Shizheng, Zhu, Lu, Jin, Wan, Dai, Yimei, Luo, Lingfei, Qu, Jianan Y., Wen, Zilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679161/
https://www.ncbi.nlm.nih.gov/pubmed/28931624
http://dx.doi.org/10.1084/jem.20170488
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author Tian, Ye
Xu, Jin
Feng, Shachuan
He, Sicong
Zhao, Shizheng
Zhu, Lu
Jin, Wan
Dai, Yimei
Luo, Lingfei
Qu, Jianan Y.
Wen, Zilong
author_facet Tian, Ye
Xu, Jin
Feng, Shachuan
He, Sicong
Zhao, Shizheng
Zhu, Lu
Jin, Wan
Dai, Yimei
Luo, Lingfei
Qu, Jianan Y.
Wen, Zilong
author_sort Tian, Ye
collection PubMed
description T lymphocytes are key cellular components of the adaptive immune system and play a central role in cell-mediated immunity in vertebrates. Despite their heterogeneities, it is believed that all different types of T lymphocytes are generated exclusively via the differentiation of hematopoietic stem cells (HSCs). Using temporal–spatial resolved fate-mapping analysis and time-lapse imaging, here we show that the ventral endothelium in the zebrafish aorta–gonad–mesonephros and posterior blood island, the hematopoietic tissues previously known to generate HSCs and erythromyeloid progenitors, respectively, gives rise to a transient wave of T lymphopoiesis independent of HSCs. This HSC-independent T lymphopoiesis occurs early and generates predominantly CD4 T(αβ) cells in the larval but not juvenile and adult stages, whereas HSC-dependent T lymphopoiesis emerges late and produces various subtypes of T lymphocytes continuously from the larval stage to adulthood. Our study unveils the existence, origin, and ontogeny of HSC-independent T lymphopoiesis in vivo and reveals the complexity of the endothelial-hematopoietic transition of the aorta.
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spelling pubmed-56791612018-05-06 The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells Tian, Ye Xu, Jin Feng, Shachuan He, Sicong Zhao, Shizheng Zhu, Lu Jin, Wan Dai, Yimei Luo, Lingfei Qu, Jianan Y. Wen, Zilong J Exp Med Research Articles T lymphocytes are key cellular components of the adaptive immune system and play a central role in cell-mediated immunity in vertebrates. Despite their heterogeneities, it is believed that all different types of T lymphocytes are generated exclusively via the differentiation of hematopoietic stem cells (HSCs). Using temporal–spatial resolved fate-mapping analysis and time-lapse imaging, here we show that the ventral endothelium in the zebrafish aorta–gonad–mesonephros and posterior blood island, the hematopoietic tissues previously known to generate HSCs and erythromyeloid progenitors, respectively, gives rise to a transient wave of T lymphopoiesis independent of HSCs. This HSC-independent T lymphopoiesis occurs early and generates predominantly CD4 T(αβ) cells in the larval but not juvenile and adult stages, whereas HSC-dependent T lymphopoiesis emerges late and produces various subtypes of T lymphocytes continuously from the larval stage to adulthood. Our study unveils the existence, origin, and ontogeny of HSC-independent T lymphopoiesis in vivo and reveals the complexity of the endothelial-hematopoietic transition of the aorta. The Rockefeller University Press 2017-11-06 /pmc/articles/PMC5679161/ /pubmed/28931624 http://dx.doi.org/10.1084/jem.20170488 Text en © 2017 Tian et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Tian, Ye
Xu, Jin
Feng, Shachuan
He, Sicong
Zhao, Shizheng
Zhu, Lu
Jin, Wan
Dai, Yimei
Luo, Lingfei
Qu, Jianan Y.
Wen, Zilong
The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title_full The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title_fullStr The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title_full_unstemmed The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title_short The first wave of T lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
title_sort first wave of t lymphopoiesis in zebrafish arises from aorta endothelium independent of hematopoietic stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679161/
https://www.ncbi.nlm.nih.gov/pubmed/28931624
http://dx.doi.org/10.1084/jem.20170488
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