Cargando…
The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish
The Wilms tumor suppressor gene Wt1 encodes a zinc finger transcription factor, which is highly conserved among vertebrates. It is a key regulator of urogenital development and homeostasis but also plays a role in other organs including the spleen and the heart. More recently additional functions fo...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786916/ https://www.ncbi.nlm.nih.gov/pubmed/35087838 http://dx.doi.org/10.3389/fcell.2021.809962 |
_version_ | 1784639247087566848 |
---|---|
author | Hopfenmüller, Vera L. Perner, Birgit Reuter, Hanna Bates, Thomas J. D. Große, Andreas Englert, Christoph |
author_facet | Hopfenmüller, Vera L. Perner, Birgit Reuter, Hanna Bates, Thomas J. D. Große, Andreas Englert, Christoph |
author_sort | Hopfenmüller, Vera L. |
collection | PubMed |
description | The Wilms tumor suppressor gene Wt1 encodes a zinc finger transcription factor, which is highly conserved among vertebrates. It is a key regulator of urogenital development and homeostasis but also plays a role in other organs including the spleen and the heart. More recently additional functions for Wt1 in the mammalian central nervous system have been described. In contrast to mammals, bony fish possess two paralogous Wt1 genes, namely wt1a and wt1b. By performing detailed in situ hybridization analyses during zebrafish development, we discovered new expression domains for wt1a in the dorsal hindbrain, the caudal medulla and the spinal cord. Marker analysis identified wt1a expressing cells of the dorsal hindbrain as ependymal cells of the choroid plexus in the myelencephalic ventricle. The choroid plexus acts as a blood-cerebrospinal fluid barrier and thus is crucial for brain homeostasis. By employing wt1a mutant larvae and a dye accumulation assay with fluorescent tracers we demonstrate that Wt1a is required for proper choroid plexus formation and function. Thus, Wt1a contributes to the barrier properties of the choroid plexus in zebrafish, revealing an unexpected role for Wt1 in the zebrafish brain. |
format | Online Article Text |
id | pubmed-8786916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87869162022-01-26 The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish Hopfenmüller, Vera L. Perner, Birgit Reuter, Hanna Bates, Thomas J. D. Große, Andreas Englert, Christoph Front Cell Dev Biol Cell and Developmental Biology The Wilms tumor suppressor gene Wt1 encodes a zinc finger transcription factor, which is highly conserved among vertebrates. It is a key regulator of urogenital development and homeostasis but also plays a role in other organs including the spleen and the heart. More recently additional functions for Wt1 in the mammalian central nervous system have been described. In contrast to mammals, bony fish possess two paralogous Wt1 genes, namely wt1a and wt1b. By performing detailed in situ hybridization analyses during zebrafish development, we discovered new expression domains for wt1a in the dorsal hindbrain, the caudal medulla and the spinal cord. Marker analysis identified wt1a expressing cells of the dorsal hindbrain as ependymal cells of the choroid plexus in the myelencephalic ventricle. The choroid plexus acts as a blood-cerebrospinal fluid barrier and thus is crucial for brain homeostasis. By employing wt1a mutant larvae and a dye accumulation assay with fluorescent tracers we demonstrate that Wt1a is required for proper choroid plexus formation and function. Thus, Wt1a contributes to the barrier properties of the choroid plexus in zebrafish, revealing an unexpected role for Wt1 in the zebrafish brain. Frontiers Media S.A. 2022-01-11 /pmc/articles/PMC8786916/ /pubmed/35087838 http://dx.doi.org/10.3389/fcell.2021.809962 Text en Copyright © 2022 Hopfenmüller, Perner, Reuter, Bates, Große and Englert. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Hopfenmüller, Vera L. Perner, Birgit Reuter, Hanna Bates, Thomas J. D. Große, Andreas Englert, Christoph The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title | The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title_full | The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title_fullStr | The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title_full_unstemmed | The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title_short | The Wilms Tumor Gene wt1a Contributes to Blood-Cerebrospinal Fluid Barrier Function in Zebrafish |
title_sort | wilms tumor gene wt1a contributes to blood-cerebrospinal fluid barrier function in zebrafish |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8786916/ https://www.ncbi.nlm.nih.gov/pubmed/35087838 http://dx.doi.org/10.3389/fcell.2021.809962 |
work_keys_str_mv | AT hopfenmullerveral thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT pernerbirgit thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT reuterhanna thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT batesthomasjd thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT großeandreas thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT englertchristoph thewilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT hopfenmullerveral wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT pernerbirgit wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT reuterhanna wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT batesthomasjd wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT großeandreas wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish AT englertchristoph wilmstumorgenewt1acontributestobloodcerebrospinalfluidbarrierfunctioninzebrafish |