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Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance

The thalamocortical projections are part of the most important higher level processing connections in the vertebrates and follow a highly ordered pathway from their origin in the thalamus to the cerebral cortex. Their functional complexities are not only due to an extremely elaborate axon guidance p...

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Autores principales: Callejas-Marin, Antuca, Moreno-Bravo, Juan Antonio, Company, Verónica, Madrigal, M. Pilar, Almagro-García, Francisca, Martínez, Salvador, Puelles, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866834/
https://www.ncbi.nlm.nih.gov/pubmed/35221935
http://dx.doi.org/10.3389/fnana.2022.830758
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author Callejas-Marin, Antuca
Moreno-Bravo, Juan Antonio
Company, Verónica
Madrigal, M. Pilar
Almagro-García, Francisca
Martínez, Salvador
Puelles, Eduardo
author_facet Callejas-Marin, Antuca
Moreno-Bravo, Juan Antonio
Company, Verónica
Madrigal, M. Pilar
Almagro-García, Francisca
Martínez, Salvador
Puelles, Eduardo
author_sort Callejas-Marin, Antuca
collection PubMed
description The thalamocortical projections are part of the most important higher level processing connections in the vertebrates and follow a highly ordered pathway from their origin in the thalamus to the cerebral cortex. Their functional complexities are not only due to an extremely elaborate axon guidance process but also due to activity-dependent mechanisms. Gli2 is an intermediary transcription factor in the Sonic hedgehog (Shh) pathway. During neural early development, Shh has an important role in dorsoventral patterning, diencephalic anteroposterior patterning, and many later developmental processes, such as axon guidance and cell migration. Using a Gli2 knockout mouse line, we have studied the role of Shh signaling mediated by Gli2 in the development of the thalamocortical projections during embryonic development. In wild-type brains, we have described the normal trajectory of the thalamocortical axons into the context of the prosomeric model. Then, we have compared it with the altered thalamocortical axons course in Gli2 homozygous embryos. The thalamocortical axons followed different trajectories and were misdirected to other territories probably due to alterations in the Robo/Slit signaling mechanism. In conclusion, the alteration of Gli2-mediated Shh signaling produces an erroneous specification of several territories related with the thalamocortical axons. This is translated into a huge modification in the pathfinding signaling mechanisms needed for the correct wiring of the thalamocortical axons.
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spelling pubmed-88668342022-02-25 Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance Callejas-Marin, Antuca Moreno-Bravo, Juan Antonio Company, Verónica Madrigal, M. Pilar Almagro-García, Francisca Martínez, Salvador Puelles, Eduardo Front Neuroanat Neuroanatomy The thalamocortical projections are part of the most important higher level processing connections in the vertebrates and follow a highly ordered pathway from their origin in the thalamus to the cerebral cortex. Their functional complexities are not only due to an extremely elaborate axon guidance process but also due to activity-dependent mechanisms. Gli2 is an intermediary transcription factor in the Sonic hedgehog (Shh) pathway. During neural early development, Shh has an important role in dorsoventral patterning, diencephalic anteroposterior patterning, and many later developmental processes, such as axon guidance and cell migration. Using a Gli2 knockout mouse line, we have studied the role of Shh signaling mediated by Gli2 in the development of the thalamocortical projections during embryonic development. In wild-type brains, we have described the normal trajectory of the thalamocortical axons into the context of the prosomeric model. Then, we have compared it with the altered thalamocortical axons course in Gli2 homozygous embryos. The thalamocortical axons followed different trajectories and were misdirected to other territories probably due to alterations in the Robo/Slit signaling mechanism. In conclusion, the alteration of Gli2-mediated Shh signaling produces an erroneous specification of several territories related with the thalamocortical axons. This is translated into a huge modification in the pathfinding signaling mechanisms needed for the correct wiring of the thalamocortical axons. Frontiers Media S.A. 2022-02-10 /pmc/articles/PMC8866834/ /pubmed/35221935 http://dx.doi.org/10.3389/fnana.2022.830758 Text en Copyright © 2022 Callejas-Marin, Moreno-Bravo, Company, Madrigal, Almagro-García, Martínez and Puelles. 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 Neuroanatomy
Callejas-Marin, Antuca
Moreno-Bravo, Juan Antonio
Company, Verónica
Madrigal, M. Pilar
Almagro-García, Francisca
Martínez, Salvador
Puelles, Eduardo
Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title_full Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title_fullStr Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title_full_unstemmed Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title_short Gli2-Mediated Shh Signaling Is Required for Thalamocortical Projection Guidance
title_sort gli2-mediated shh signaling is required for thalamocortical projection guidance
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866834/
https://www.ncbi.nlm.nih.gov/pubmed/35221935
http://dx.doi.org/10.3389/fnana.2022.830758
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