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Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta
Ectothermal reptiles have internal pigmentation, which is not seen in endothermal birds and mammals. Here we show that the development of the dorsal neural tube-derived melanoblasts in turtle Trachemys scripta is regulated by similar mechanisms as in other amniotes, but significantly later in develo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608706/ https://www.ncbi.nlm.nih.gov/pubmed/28935865 http://dx.doi.org/10.1038/s41598-017-12352-0 |
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author | Rice, Ritva Cebra-Thomas, Judith Haugas, Maarja Partanen, Juha Rice, David P. C. Gilbert, Scott F. |
author_facet | Rice, Ritva Cebra-Thomas, Judith Haugas, Maarja Partanen, Juha Rice, David P. C. Gilbert, Scott F. |
author_sort | Rice, Ritva |
collection | PubMed |
description | Ectothermal reptiles have internal pigmentation, which is not seen in endothermal birds and mammals. Here we show that the development of the dorsal neural tube-derived melanoblasts in turtle Trachemys scripta is regulated by similar mechanisms as in other amniotes, but significantly later in development, during the second phase of turtle trunk neural crest emigration. The development of melanoblasts coincided with a morphological change in the dorsal neural tube between stages mature G15 and G16. The melanoblasts delaminated and gathered in the carapacial staging area above the neural tube at G16, and differentiated into pigment-forming melanocytes during in vitro culture. The Mitf-positive melanoblasts were not restricted to the dorsolateral pathway as in birds and mammals but were also present medially through the somites similarly to ectothermal anamniotes. This matched a lack of environmental barrier dorsal and lateral to neural tube and the somites that is normally formed by PNA-binding proteins that block entry to medial pathways. PNA-binding proteins may also participate in the patterning of the carapacial pigmentation as both the migratory neural crest cells and pigment localized only to PNA-free areas. |
format | Online Article Text |
id | pubmed-5608706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56087062017-10-04 Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta Rice, Ritva Cebra-Thomas, Judith Haugas, Maarja Partanen, Juha Rice, David P. C. Gilbert, Scott F. Sci Rep Article Ectothermal reptiles have internal pigmentation, which is not seen in endothermal birds and mammals. Here we show that the development of the dorsal neural tube-derived melanoblasts in turtle Trachemys scripta is regulated by similar mechanisms as in other amniotes, but significantly later in development, during the second phase of turtle trunk neural crest emigration. The development of melanoblasts coincided with a morphological change in the dorsal neural tube between stages mature G15 and G16. The melanoblasts delaminated and gathered in the carapacial staging area above the neural tube at G16, and differentiated into pigment-forming melanocytes during in vitro culture. The Mitf-positive melanoblasts were not restricted to the dorsolateral pathway as in birds and mammals but were also present medially through the somites similarly to ectothermal anamniotes. This matched a lack of environmental barrier dorsal and lateral to neural tube and the somites that is normally formed by PNA-binding proteins that block entry to medial pathways. PNA-binding proteins may also participate in the patterning of the carapacial pigmentation as both the migratory neural crest cells and pigment localized only to PNA-free areas. Nature Publishing Group UK 2017-09-21 /pmc/articles/PMC5608706/ /pubmed/28935865 http://dx.doi.org/10.1038/s41598-017-12352-0 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Rice, Ritva Cebra-Thomas, Judith Haugas, Maarja Partanen, Juha Rice, David P. C. Gilbert, Scott F. Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title | Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title_full | Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title_fullStr | Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title_full_unstemmed | Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title_short | Melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle Trachemys scripta |
title_sort | melanoblast development coincides with the late emerging cells from the dorsal neural tube in turtle trachemys scripta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608706/ https://www.ncbi.nlm.nih.gov/pubmed/28935865 http://dx.doi.org/10.1038/s41598-017-12352-0 |
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