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Development and growth of organs in living whole embryo and larval grafts in zebrafish
Age-related systemic environments influence neurogenesis and organ regeneration of heterochronic parabiotic partners; however, the difficulty of manipulating small embryos prevents the effects of aged systemic environments on primitive organs at the developmental stage from being analysed. Here, we...
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/PMC5705650/ https://www.ncbi.nlm.nih.gov/pubmed/29184141 http://dx.doi.org/10.1038/s41598-017-16642-5 |
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author | Kawasaki, Toshihiro Maeno, Akiteru Shiroishi, Toshihiko Sakai, Noriyoshi |
author_facet | Kawasaki, Toshihiro Maeno, Akiteru Shiroishi, Toshihiko Sakai, Noriyoshi |
author_sort | Kawasaki, Toshihiro |
collection | PubMed |
description | Age-related systemic environments influence neurogenesis and organ regeneration of heterochronic parabiotic partners; however, the difficulty of manipulating small embryos prevents the effects of aged systemic environments on primitive organs at the developmental stage from being analysed. Here, we describe a novel transplantation system to support whole living embryos/larvae as grafts in immunodeficient zebrafish by the intrusion of host blood vessels into the grafts, allowing bodies similar to those of heterochronic parabiosis to be generated by subcutaneous grafting. Although grafted embryos/larvae formed most organs, not all organogenesis was supported equally; although the brain, eyes and the intestine usually developed, the liver, testes and heart developed insufficiently or even occasionally disappeared. Removal of host germ cells stimulated testis development in grafted embryos. These results indicate that primitive testes are susceptible to the systemic environments that originated from the germ cells of aged hosts and imply that the primitive liver and heart are similar. Upon applying this method to embryonic lethal mutants, various types of organs, including testes that developed in germ-cell-removed recipients, and viable offspring were obtained from the mutants. This unique transplantation system will lead to new insights into the age-related systemic environments that are crucial for organogenesis in vertebrates. |
format | Online Article Text |
id | pubmed-5705650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57056502017-12-05 Development and growth of organs in living whole embryo and larval grafts in zebrafish Kawasaki, Toshihiro Maeno, Akiteru Shiroishi, Toshihiko Sakai, Noriyoshi Sci Rep Article Age-related systemic environments influence neurogenesis and organ regeneration of heterochronic parabiotic partners; however, the difficulty of manipulating small embryos prevents the effects of aged systemic environments on primitive organs at the developmental stage from being analysed. Here, we describe a novel transplantation system to support whole living embryos/larvae as grafts in immunodeficient zebrafish by the intrusion of host blood vessels into the grafts, allowing bodies similar to those of heterochronic parabiosis to be generated by subcutaneous grafting. Although grafted embryos/larvae formed most organs, not all organogenesis was supported equally; although the brain, eyes and the intestine usually developed, the liver, testes and heart developed insufficiently or even occasionally disappeared. Removal of host germ cells stimulated testis development in grafted embryos. These results indicate that primitive testes are susceptible to the systemic environments that originated from the germ cells of aged hosts and imply that the primitive liver and heart are similar. Upon applying this method to embryonic lethal mutants, various types of organs, including testes that developed in germ-cell-removed recipients, and viable offspring were obtained from the mutants. This unique transplantation system will lead to new insights into the age-related systemic environments that are crucial for organogenesis in vertebrates. Nature Publishing Group UK 2017-11-28 /pmc/articles/PMC5705650/ /pubmed/29184141 http://dx.doi.org/10.1038/s41598-017-16642-5 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 Kawasaki, Toshihiro Maeno, Akiteru Shiroishi, Toshihiko Sakai, Noriyoshi Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title | Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title_full | Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title_fullStr | Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title_full_unstemmed | Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title_short | Development and growth of organs in living whole embryo and larval grafts in zebrafish |
title_sort | development and growth of organs in living whole embryo and larval grafts in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705650/ https://www.ncbi.nlm.nih.gov/pubmed/29184141 http://dx.doi.org/10.1038/s41598-017-16642-5 |
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