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Restricted expression of classic cadherins in the spinal cord of the chicken embryo

Classic cadherins belong to the family of cadherin genes and play important roles in neurogenesis, neuron migration, and axon growth. In the present study, we compared the expression patterns of 10 classic cadherins (Cdh2, Cdh4, Cdh6, Cdh7, Cdh8, Cdh9, Cdh11, Cdh12, Cdh18, and Cdh20) in the developi...

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Autores principales: Lin, Juntang, Wang, Congrui, Redies, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978366/
https://www.ncbi.nlm.nih.gov/pubmed/24744704
http://dx.doi.org/10.3389/fnana.2014.00018
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author Lin, Juntang
Wang, Congrui
Redies, Christoph
author_facet Lin, Juntang
Wang, Congrui
Redies, Christoph
author_sort Lin, Juntang
collection PubMed
description Classic cadherins belong to the family of cadherin genes and play important roles in neurogenesis, neuron migration, and axon growth. In the present study, we compared the expression patterns of 10 classic cadherins (Cdh2, Cdh4, Cdh6, Cdh7, Cdh8, Cdh9, Cdh11, Cdh12, Cdh18, and Cdh20) in the developing chicken spinal cord (SP) by in situ hybridization. Our results indicate that each of the investigated cadherins exhibits a spatially restricted and temporally regulated pattern of expression. At early developmental stages (E2.5–E3), Cdh2 is expressed throughout the neuroepithelial layer. Cdh6 is strongly positive in the roof plate and later also in the floor plate. Cdh7, Cdh11, Cdh12, and Cdh20 are expressed in restricted regions of the basal plate of the SP. At intermediate stages of development (E4–E10), specific expression profiles are observed for all investigated cadherins in the differentiating mantle layer along the dorsoventral, mediolateral, and rostrocaudal dimensions. Expression profiles are especially diverse for Cdh2, Cdh4, Cdh8, Cdh11, and Cdh20 in the dorsal horn, while different pools of motor neurons exhibit signal for Cdh6, Cdh7, Cdh8, Cdh9, Cdh12, and Cdh20 in the ventral horn. Interestingly, subpopulations of cells in the dorsal root ganglion express combinations of different cadherins. In the surrounding tissues, such as the boundary cap cells and the notochord, the cadherins are also expressed differentially. The highly regulated spatiotemporal expression patterns of the classic cadherins indicate that these genes potentially play multiple and diverse roles during the development of the SP and its surrounding tissues.
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spelling pubmed-39783662014-04-17 Restricted expression of classic cadherins in the spinal cord of the chicken embryo Lin, Juntang Wang, Congrui Redies, Christoph Front Neuroanat Neuroscience Classic cadherins belong to the family of cadherin genes and play important roles in neurogenesis, neuron migration, and axon growth. In the present study, we compared the expression patterns of 10 classic cadherins (Cdh2, Cdh4, Cdh6, Cdh7, Cdh8, Cdh9, Cdh11, Cdh12, Cdh18, and Cdh20) in the developing chicken spinal cord (SP) by in situ hybridization. Our results indicate that each of the investigated cadherins exhibits a spatially restricted and temporally regulated pattern of expression. At early developmental stages (E2.5–E3), Cdh2 is expressed throughout the neuroepithelial layer. Cdh6 is strongly positive in the roof plate and later also in the floor plate. Cdh7, Cdh11, Cdh12, and Cdh20 are expressed in restricted regions of the basal plate of the SP. At intermediate stages of development (E4–E10), specific expression profiles are observed for all investigated cadherins in the differentiating mantle layer along the dorsoventral, mediolateral, and rostrocaudal dimensions. Expression profiles are especially diverse for Cdh2, Cdh4, Cdh8, Cdh11, and Cdh20 in the dorsal horn, while different pools of motor neurons exhibit signal for Cdh6, Cdh7, Cdh8, Cdh9, Cdh12, and Cdh20 in the ventral horn. Interestingly, subpopulations of cells in the dorsal root ganglion express combinations of different cadherins. In the surrounding tissues, such as the boundary cap cells and the notochord, the cadherins are also expressed differentially. The highly regulated spatiotemporal expression patterns of the classic cadherins indicate that these genes potentially play multiple and diverse roles during the development of the SP and its surrounding tissues. Frontiers Media S.A. 2014-03-31 /pmc/articles/PMC3978366/ /pubmed/24744704 http://dx.doi.org/10.3389/fnana.2014.00018 Text en Copyright © 2014 Lin, Wang and Redies. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Lin, Juntang
Wang, Congrui
Redies, Christoph
Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title_full Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title_fullStr Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title_full_unstemmed Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title_short Restricted expression of classic cadherins in the spinal cord of the chicken embryo
title_sort restricted expression of classic cadherins in the spinal cord of the chicken embryo
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978366/
https://www.ncbi.nlm.nih.gov/pubmed/24744704
http://dx.doi.org/10.3389/fnana.2014.00018
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