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Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain

BACKGROUND: A fundamental requirement for development of diverse brain regions is the function of local organizers at morphological boundaries. These organizers are restricted groups of cells that secrete signaling molecules, which in turn regulate the fate of the adjacent neural tissue. The thalamu...

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Autores principales: Mattes, Benjamin, Weber, Sabrina, Peres, João, Chen, Qing, Davidson, Gary, Houart, Corinne, Scholpp, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349543/
https://www.ncbi.nlm.nih.gov/pubmed/22475147
http://dx.doi.org/10.1186/1749-8104-7-12
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author Mattes, Benjamin
Weber, Sabrina
Peres, João
Chen, Qing
Davidson, Gary
Houart, Corinne
Scholpp, Steffen
author_facet Mattes, Benjamin
Weber, Sabrina
Peres, João
Chen, Qing
Davidson, Gary
Houart, Corinne
Scholpp, Steffen
author_sort Mattes, Benjamin
collection PubMed
description BACKGROUND: A fundamental requirement for development of diverse brain regions is the function of local organizers at morphological boundaries. These organizers are restricted groups of cells that secrete signaling molecules, which in turn regulate the fate of the adjacent neural tissue. The thalamus is located in the caudal diencephalon and is the central relay station between the sense organs and higher brain areas. The mid-diencephalic organizer (MDO) orchestrates the development of the thalamus by releasing secreted signaling molecules such as Shh. RESULTS: Here we show that canonical Wnt signaling in the caudal forebrain is required for the formation of the Shh-secreting MD organizer in zebrafish. Wnt signaling induces the MDO in a narrow time window of 4 hours - between 10 and 14 hours post fertilization. Loss of Wnt3 and Wnt3a prevents induction of the MDO, a phenotype also observed upon blockage of canonical Wnt signaling per se. Pharmaceutical activation of the canonical Wnt pathways in Wnt3/Wnt3a compound morphant embryos is able to restore the lack of the MDO. After blockage of Wnt signaling or knock-down of Wnt3/Wnt3a we find an increase of apoptotic cells specifically within the organizer primordium. Consistently, blockage of apoptosis restores the thalamus organizer MDO in Wnt deficient embryos. CONCLUSION: We have identified canonical Wnt signaling as a novel pathway, that is required for proper formation of the MDO and consequently for the development of the major relay station of the brain - the thalamus. We propose that Wnt ligands are necessary to maintain the primordial tissue of the organizer during somitogenesis by suppressing Tp53-mediated apoptosis.
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spelling pubmed-33495432012-05-11 Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain Mattes, Benjamin Weber, Sabrina Peres, João Chen, Qing Davidson, Gary Houart, Corinne Scholpp, Steffen Neural Dev Research Article BACKGROUND: A fundamental requirement for development of diverse brain regions is the function of local organizers at morphological boundaries. These organizers are restricted groups of cells that secrete signaling molecules, which in turn regulate the fate of the adjacent neural tissue. The thalamus is located in the caudal diencephalon and is the central relay station between the sense organs and higher brain areas. The mid-diencephalic organizer (MDO) orchestrates the development of the thalamus by releasing secreted signaling molecules such as Shh. RESULTS: Here we show that canonical Wnt signaling in the caudal forebrain is required for the formation of the Shh-secreting MD organizer in zebrafish. Wnt signaling induces the MDO in a narrow time window of 4 hours - between 10 and 14 hours post fertilization. Loss of Wnt3 and Wnt3a prevents induction of the MDO, a phenotype also observed upon blockage of canonical Wnt signaling per se. Pharmaceutical activation of the canonical Wnt pathways in Wnt3/Wnt3a compound morphant embryos is able to restore the lack of the MDO. After blockage of Wnt signaling or knock-down of Wnt3/Wnt3a we find an increase of apoptotic cells specifically within the organizer primordium. Consistently, blockage of apoptosis restores the thalamus organizer MDO in Wnt deficient embryos. CONCLUSION: We have identified canonical Wnt signaling as a novel pathway, that is required for proper formation of the MDO and consequently for the development of the major relay station of the brain - the thalamus. We propose that Wnt ligands are necessary to maintain the primordial tissue of the organizer during somitogenesis by suppressing Tp53-mediated apoptosis. BioMed Central 2012-04-04 /pmc/articles/PMC3349543/ /pubmed/22475147 http://dx.doi.org/10.1186/1749-8104-7-12 Text en Copyright ©2012 Mattes et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mattes, Benjamin
Weber, Sabrina
Peres, João
Chen, Qing
Davidson, Gary
Houart, Corinne
Scholpp, Steffen
Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title_full Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title_fullStr Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title_full_unstemmed Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title_short Wnt3 and Wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
title_sort wnt3 and wnt3a are required for induction of the mid-diencephalic organizer in the caudal forebrain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349543/
https://www.ncbi.nlm.nih.gov/pubmed/22475147
http://dx.doi.org/10.1186/1749-8104-7-12
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