Divergence of zebrafish and mouse lymphatic cell fate specification pathways
In mammals, the homeodomain transcription factor Prox1 acts as the central regulator of lymphatic cell fate. Its restricted expression in a subset of cardinal vein cells leads to a switch towards lymphatic specification and hence represents a prerequisite for the initiation of lymphangiogenesis. Mur...
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sg-ntu-dr.10356-1015492022-02-16T16:27:52Z Divergence of zebrafish and mouse lymphatic cell fate specification pathways Impel, Andreas van Zhao, Zhonghua Hermkens, Dorien M. A. Roukens, M. Guy Fischer, Johanna C. Peterson-Maduro, Josi Duckers, Henricus Ober, Elke A. Ingham, Philip William Schulte-Merker, Stefan Lee Kong Chian School of Medicine (LKCMedicine) DRNTU::Science::Biological sciences::Zoology::Anatomy In mammals, the homeodomain transcription factor Prox1 acts as the central regulator of lymphatic cell fate. Its restricted expression in a subset of cardinal vein cells leads to a switch towards lymphatic specification and hence represents a prerequisite for the initiation of lymphangiogenesis. Murine Prox1-null embryos lack lymphatic structures, and sustained expression of Prox1 is indispensable for the maintenance of lymphatic cell fate even at adult stages, highlighting the unique importance of this gene for the lymphatic lineage. Whether this pre-eminent role of Prox1 within the lymphatic vasculature is conserved in other vertebrate classes has remained unresolved, mainly owing to the lack of availability of loss-of-function mutants. Here, we re-examine the role of Prox1a in zebrafish lymphangiogenesis. First, using a transgenic reporter line, we show that prox1a is initially expressed in different endothelial compartments, becoming restricted to lymphatic endothelial cells only at later stages. Second, using targeted mutagenesis, we show that Prox1a is dispensable for lymphatic specification and subsequent lymphangiogenesis in zebrafish. In line with this result, we found that the functionally related transcription factors Coup-TFII and Sox18 are also dispensable for lymphangiogenesis. Together, these findings suggest that lymphatic commitment in zebrafish and mice is controlled in fundamentally different ways. ASTAR (Agency for Sci., Tech. and Research, S’pore) Accepted version 2014-10-30T02:17:39Z 2019-12-06T20:40:26Z 2014-10-30T02:17:39Z 2019-12-06T20:40:26Z 2014 2014 Journal Article Impel, A. v., Zhao, Z., Hermkens, D. M. A., Roukens, M. G., Fischer, J. C., Peterson-Maduro, J., et al. (2014). Divergence of zebrafish and mouse lymphatic cell fate specification pathways. Development, 141(6), 1228-1238. https://hdl.handle.net/10356/101549 http://hdl.handle.net/10220/24154 10.1242/dev.105031 24523456 en Development © 2014 The Authors(published by The Company of Biologists Ltd.) This is the author created version of a work that has been peer reviewed and accepted for publication in Development, published by The Company of Biologists Ltd. on behalf of The Authors. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1242/dev.105031]. 28 p. application/pdf |
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DRNTU::Science::Biological sciences::Zoology::Anatomy Impel, Andreas van Zhao, Zhonghua Hermkens, Dorien M. A. Roukens, M. Guy Fischer, Johanna C. Peterson-Maduro, Josi Duckers, Henricus Ober, Elke A. Ingham, Philip William Schulte-Merker, Stefan Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
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In mammals, the homeodomain transcription factor Prox1 acts as the central regulator of lymphatic cell fate. Its restricted expression in a subset of cardinal vein cells leads to a switch towards lymphatic specification and hence represents a prerequisite for the initiation of lymphangiogenesis. Murine Prox1-null embryos lack lymphatic structures, and sustained expression of Prox1 is indispensable for the maintenance of lymphatic cell fate even at adult stages, highlighting the unique importance of this gene for the lymphatic lineage. Whether this pre-eminent role of Prox1 within the lymphatic vasculature is conserved in other vertebrate classes has remained unresolved, mainly owing to the lack of availability of loss-of-function mutants. Here, we re-examine the role of Prox1a in zebrafish lymphangiogenesis. First, using a transgenic reporter line, we show that prox1a is initially expressed in different endothelial compartments, becoming restricted to lymphatic endothelial cells only at later stages. Second, using targeted mutagenesis, we show that Prox1a is dispensable for lymphatic specification and subsequent lymphangiogenesis in zebrafish. In line with this result, we found that the functionally related transcription factors Coup-TFII and Sox18 are also dispensable for lymphangiogenesis. Together, these findings suggest that lymphatic commitment in zebrafish and mice is controlled in fundamentally different ways. |
author2 |
Lee Kong Chian School of Medicine (LKCMedicine) |
author_facet |
Lee Kong Chian School of Medicine (LKCMedicine) Impel, Andreas van Zhao, Zhonghua Hermkens, Dorien M. A. Roukens, M. Guy Fischer, Johanna C. Peterson-Maduro, Josi Duckers, Henricus Ober, Elke A. Ingham, Philip William Schulte-Merker, Stefan |
format |
Article |
author |
Impel, Andreas van Zhao, Zhonghua Hermkens, Dorien M. A. Roukens, M. Guy Fischer, Johanna C. Peterson-Maduro, Josi Duckers, Henricus Ober, Elke A. Ingham, Philip William Schulte-Merker, Stefan |
author_sort |
Impel, Andreas van |
title |
Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
title_short |
Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
title_full |
Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
title_fullStr |
Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
title_full_unstemmed |
Divergence of zebrafish and mouse lymphatic cell fate specification pathways |
title_sort |
divergence of zebrafish and mouse lymphatic cell fate specification pathways |
publishDate |
2014 |
url |
https://hdl.handle.net/10356/101549 http://hdl.handle.net/10220/24154 |
_version_ |
1725985689036652544 |