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Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure

Vertebrate color vision is predominantly mediated by the presence of multiple cone photoreceptor subtypes that are each maximally sensitive to different wavelengths of light. Thyroid hormone (TH) has been shown to be essential in the spatiotemporal patterning of cone subtypes in many species, includ...

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Autores principales: Farre, Ashley A., Thomas, Preston, Huang, Johnson, Poulsen, Rachel A., Owusu Poku, Emmanuel, Stenkamp, Deborah L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514274/
https://www.ncbi.nlm.nih.gov/pubmed/37735192
http://dx.doi.org/10.1038/s41598-023-42686-x
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author Farre, Ashley A.
Thomas, Preston
Huang, Johnson
Poulsen, Rachel A.
Owusu Poku, Emmanuel
Stenkamp, Deborah L.
author_facet Farre, Ashley A.
Thomas, Preston
Huang, Johnson
Poulsen, Rachel A.
Owusu Poku, Emmanuel
Stenkamp, Deborah L.
author_sort Farre, Ashley A.
collection PubMed
description Vertebrate color vision is predominantly mediated by the presence of multiple cone photoreceptor subtypes that are each maximally sensitive to different wavelengths of light. Thyroid hormone (TH) has been shown to be essential in the spatiotemporal patterning of cone subtypes in many species, including cone subtypes that express opsins that are encoded by tandemly replicated genes. TH has been shown to differentially regulate the tandemly replicated lws opsin genes in zebrafish, and exogenous treatments alter the expression levels of these genes in larvae and juveniles. In this study, we sought to determine whether gene expression in cone photoreceptors remains plastic to TH treatment in adults. We used a transgenic lws reporter line, multiplexed fluorescence hybridization chain reaction in situ hybridization, and qPCR to examine the extent to which cone gene expression can be altered by TH in adults. Our studies revealed that opsin gene expression, and the expression of other photoreceptor genes, remains plastic to TH treatment in adult zebrafish. In addition to retinal plasticity, exogenous TH treatment alters skin pigmentation patterns in adult zebrafish after 5 days. Taken together, our results show a remarkable level of TH-sensitive plasticity in the adult zebrafish.
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spelling pubmed-105142742023-09-23 Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure Farre, Ashley A. Thomas, Preston Huang, Johnson Poulsen, Rachel A. Owusu Poku, Emmanuel Stenkamp, Deborah L. Sci Rep Article Vertebrate color vision is predominantly mediated by the presence of multiple cone photoreceptor subtypes that are each maximally sensitive to different wavelengths of light. Thyroid hormone (TH) has been shown to be essential in the spatiotemporal patterning of cone subtypes in many species, including cone subtypes that express opsins that are encoded by tandemly replicated genes. TH has been shown to differentially regulate the tandemly replicated lws opsin genes in zebrafish, and exogenous treatments alter the expression levels of these genes in larvae and juveniles. In this study, we sought to determine whether gene expression in cone photoreceptors remains plastic to TH treatment in adults. We used a transgenic lws reporter line, multiplexed fluorescence hybridization chain reaction in situ hybridization, and qPCR to examine the extent to which cone gene expression can be altered by TH in adults. Our studies revealed that opsin gene expression, and the expression of other photoreceptor genes, remains plastic to TH treatment in adult zebrafish. In addition to retinal plasticity, exogenous TH treatment alters skin pigmentation patterns in adult zebrafish after 5 days. Taken together, our results show a remarkable level of TH-sensitive plasticity in the adult zebrafish. Nature Publishing Group UK 2023-09-21 /pmc/articles/PMC10514274/ /pubmed/37735192 http://dx.doi.org/10.1038/s41598-023-42686-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Farre, Ashley A.
Thomas, Preston
Huang, Johnson
Poulsen, Rachel A.
Owusu Poku, Emmanuel
Stenkamp, Deborah L.
Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title_full Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title_fullStr Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title_full_unstemmed Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title_short Plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
title_sort plasticity of cone photoreceptors in adult zebrafish revealed by thyroid hormone exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514274/
https://www.ncbi.nlm.nih.gov/pubmed/37735192
http://dx.doi.org/10.1038/s41598-023-42686-x
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