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Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish

Colour patterns of adult fish are produced by several types of pigment cells that distribute in the dermis during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed by light stripes of xanthophores. Mutants lacking either cell t...

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Autores principales: Frohnhöfer, Hans Georg, Krauss, Jana, Maischein, Hans-Martin, Nüsslein-Volhard, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Company of Biologists 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912879/
https://www.ncbi.nlm.nih.gov/pubmed/23821036
http://dx.doi.org/10.1242/dev.096719
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author Frohnhöfer, Hans Georg
Krauss, Jana
Maischein, Hans-Martin
Nüsslein-Volhard, Christiane
author_facet Frohnhöfer, Hans Georg
Krauss, Jana
Maischein, Hans-Martin
Nüsslein-Volhard, Christiane
author_sort Frohnhöfer, Hans Georg
collection PubMed
description Colour patterns of adult fish are produced by several types of pigment cells that distribute in the dermis during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed by light stripes of xanthophores. Mutants lacking either cell type do not form proper stripes, indicating that interactions between these two chromatophore types are required for stripe formation. A third cell type, silvery iridophores, participates to render a shiny appearance to the pattern, but its role in stripe formation has been unclear. Mutations in rose (rse) or shady (shd) cause a lack or strong reduction of iridophores in adult fish; in addition, the melanophore number is drastically reduced and stripes are broken up into spots. We show that rse and shd are autonomously required in iridophores, as mutant melanophores form normal sized stripes when confronted with wild-type iridophores in chimeric animals. We describe stripe formation in mutants missing one or two of the three chromatophore types. None of the chromatophore types alone is able to create a pattern but residual stripe formation occurs with two cell types. Our analysis shows that iridophores promote and sustain melanophores. Furthermore, iridophores attract xanthophores, whereas xanthophores repel melanophores. We present a model for the interactions between the three chromatophore types underlying stripe formation. Stripe formation is initiated by iridophores appearing at the horizontal myoseptum, which serves as a morphological landmark for stripe orientation, but is subsequently a self-organising process.
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spelling pubmed-39128792014-02-11 Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish Frohnhöfer, Hans Georg Krauss, Jana Maischein, Hans-Martin Nüsslein-Volhard, Christiane Development Research Articles Colour patterns of adult fish are produced by several types of pigment cells that distribute in the dermis during juvenile development. The zebrafish, Danio rerio, displays a striking pattern of dark stripes of melanophores interspersed by light stripes of xanthophores. Mutants lacking either cell type do not form proper stripes, indicating that interactions between these two chromatophore types are required for stripe formation. A third cell type, silvery iridophores, participates to render a shiny appearance to the pattern, but its role in stripe formation has been unclear. Mutations in rose (rse) or shady (shd) cause a lack or strong reduction of iridophores in adult fish; in addition, the melanophore number is drastically reduced and stripes are broken up into spots. We show that rse and shd are autonomously required in iridophores, as mutant melanophores form normal sized stripes when confronted with wild-type iridophores in chimeric animals. We describe stripe formation in mutants missing one or two of the three chromatophore types. None of the chromatophore types alone is able to create a pattern but residual stripe formation occurs with two cell types. Our analysis shows that iridophores promote and sustain melanophores. Furthermore, iridophores attract xanthophores, whereas xanthophores repel melanophores. We present a model for the interactions between the three chromatophore types underlying stripe formation. Stripe formation is initiated by iridophores appearing at the horizontal myoseptum, which serves as a morphological landmark for stripe orientation, but is subsequently a self-organising process. Company of Biologists 2013-07-15 /pmc/articles/PMC3912879/ /pubmed/23821036 http://dx.doi.org/10.1242/dev.096719 Text en © 2013. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/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 Articles
Frohnhöfer, Hans Georg
Krauss, Jana
Maischein, Hans-Martin
Nüsslein-Volhard, Christiane
Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title_full Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title_fullStr Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title_full_unstemmed Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title_short Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
title_sort iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912879/
https://www.ncbi.nlm.nih.gov/pubmed/23821036
http://dx.doi.org/10.1242/dev.096719
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