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Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function

The isthmic organizer (IsO) is a signaling center that specifies the correct and distinct embryonic development of the dopaminergic midbrain and serotonergic hindbrain. The IsO is a linear boundary between the two brain regions, emerging at around embryonic day 7-8 of murine embryonic development, t...

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Autores principales: Kouwenhoven, Willemieke M., Veenvliet, Jesse V., van Hooft, Johannes A., van der Heide, L. P., Smidt, Marten P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810741/
https://www.ncbi.nlm.nih.gov/pubmed/26879466
http://dx.doi.org/10.1242/bio.015032
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author Kouwenhoven, Willemieke M.
Veenvliet, Jesse V.
van Hooft, Johannes A.
van der Heide, L. P.
Smidt, Marten P.
author_facet Kouwenhoven, Willemieke M.
Veenvliet, Jesse V.
van Hooft, Johannes A.
van der Heide, L. P.
Smidt, Marten P.
author_sort Kouwenhoven, Willemieke M.
collection PubMed
description The isthmic organizer (IsO) is a signaling center that specifies the correct and distinct embryonic development of the dopaminergic midbrain and serotonergic hindbrain. The IsO is a linear boundary between the two brain regions, emerging at around embryonic day 7-8 of murine embryonic development, that shapes its surroundings through the expression of instructive signals such as Wnt and growth factors. Homeobox transcription factor engrailed 1 (En1) is present in midbrain and rostral hindbrain (i.e. rhombomere 1, R1). Its expression spans the IsO, and it is known to be an important survival factor for both dopaminergic and serotonergic neurons. Erroneous composition of dopaminergic neurons in the midbrain or serotonergic neurons in the hindbrain is associated with severe pathologies such as Parkinson's disease, depression or autism. Here we investigated the role of En1 in early mid-hindbrain development, using multiple En1-ablated mouse models as well as lineage-tracing techniques, and observed the appearance of ectopic dopaminergic neurons, indistinguishable from midbrain dopaminergic neurons based on molecular profile and intrinsic electrophysiological properties. We propose that this change is the direct result of a caudal relocation of the IsO as represented by ectopic presence of Fgf8, Otx2, Wnt1 and canonical Wnt-signalling. Our work suggests a newly-discovered role for En1: the repression of Otx2, Wnt1 and canonical Wnt-signaling in R1. Overall, our results suggest that En1 is essential for proper IsO maintenance and function.
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spelling pubmed-48107412016-04-04 Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function Kouwenhoven, Willemieke M. Veenvliet, Jesse V. van Hooft, Johannes A. van der Heide, L. P. Smidt, Marten P. Biol Open Research Article The isthmic organizer (IsO) is a signaling center that specifies the correct and distinct embryonic development of the dopaminergic midbrain and serotonergic hindbrain. The IsO is a linear boundary between the two brain regions, emerging at around embryonic day 7-8 of murine embryonic development, that shapes its surroundings through the expression of instructive signals such as Wnt and growth factors. Homeobox transcription factor engrailed 1 (En1) is present in midbrain and rostral hindbrain (i.e. rhombomere 1, R1). Its expression spans the IsO, and it is known to be an important survival factor for both dopaminergic and serotonergic neurons. Erroneous composition of dopaminergic neurons in the midbrain or serotonergic neurons in the hindbrain is associated with severe pathologies such as Parkinson's disease, depression or autism. Here we investigated the role of En1 in early mid-hindbrain development, using multiple En1-ablated mouse models as well as lineage-tracing techniques, and observed the appearance of ectopic dopaminergic neurons, indistinguishable from midbrain dopaminergic neurons based on molecular profile and intrinsic electrophysiological properties. We propose that this change is the direct result of a caudal relocation of the IsO as represented by ectopic presence of Fgf8, Otx2, Wnt1 and canonical Wnt-signalling. Our work suggests a newly-discovered role for En1: the repression of Otx2, Wnt1 and canonical Wnt-signaling in R1. Overall, our results suggest that En1 is essential for proper IsO maintenance and function. The Company of Biologists Ltd 2016-02-15 /pmc/articles/PMC4810741/ /pubmed/26879466 http://dx.doi.org/10.1242/bio.015032 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Kouwenhoven, Willemieke M.
Veenvliet, Jesse V.
van Hooft, Johannes A.
van der Heide, L. P.
Smidt, Marten P.
Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title_full Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title_fullStr Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title_full_unstemmed Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title_short Engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
title_sort engrailed 1 shapes the dopaminergic and serotonergic landscape through proper isthmic organizer maintenance and function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810741/
https://www.ncbi.nlm.nih.gov/pubmed/26879466
http://dx.doi.org/10.1242/bio.015032
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