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Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells
Lizards regenerate amputated tails but fail to recapitulate the dorsoventral patterning achieved during embryonic development. Regenerated lizard tails form ependymal tubes (ETs) that, like embryonic tail neural tubes (NTs), induce cartilage differentiation in surrounding cells via sonic hedgehog (S...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516916/ https://www.ncbi.nlm.nih.gov/pubmed/34650077 http://dx.doi.org/10.1038/s41467-021-26321-9 |
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author | Lozito, Thomas P. Londono, Ricardo Sun, Aaron X. Hudnall, Megan L. |
author_facet | Lozito, Thomas P. Londono, Ricardo Sun, Aaron X. Hudnall, Megan L. |
author_sort | Lozito, Thomas P. |
collection | PubMed |
description | Lizards regenerate amputated tails but fail to recapitulate the dorsoventral patterning achieved during embryonic development. Regenerated lizard tails form ependymal tubes (ETs) that, like embryonic tail neural tubes (NTs), induce cartilage differentiation in surrounding cells via sonic hedgehog (Shh) signaling. However, adult ETs lack characteristically roof plate-associated structures and express Shh throughout their circumferences, resulting in the formation of unpatterned cartilage tubes. Both NTs and ETs contain neural stem cells (NSCs), but only embryonic NSC populations differentiate into roof plate identities when protected from endogenous Hedgehog signaling. NSCs were isolated from parthenogenetic lizard embryos, rendered unresponsive to Hedgehog signaling via CRISPR/Cas9 gene knockout of smoothened (Smo), and implanted back into clonally-identical adults to regulate tail regeneration. Here we report that Smo knockout embryonic NSCs oppose cartilage formation when engrafted to adult ETs, representing an important milestone in the creation of regenerated lizard tails with dorsoventrally patterned skeletal tissues. |
format | Online Article Text |
id | pubmed-8516916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85169162021-10-29 Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells Lozito, Thomas P. Londono, Ricardo Sun, Aaron X. Hudnall, Megan L. Nat Commun Article Lizards regenerate amputated tails but fail to recapitulate the dorsoventral patterning achieved during embryonic development. Regenerated lizard tails form ependymal tubes (ETs) that, like embryonic tail neural tubes (NTs), induce cartilage differentiation in surrounding cells via sonic hedgehog (Shh) signaling. However, adult ETs lack characteristically roof plate-associated structures and express Shh throughout their circumferences, resulting in the formation of unpatterned cartilage tubes. Both NTs and ETs contain neural stem cells (NSCs), but only embryonic NSC populations differentiate into roof plate identities when protected from endogenous Hedgehog signaling. NSCs were isolated from parthenogenetic lizard embryos, rendered unresponsive to Hedgehog signaling via CRISPR/Cas9 gene knockout of smoothened (Smo), and implanted back into clonally-identical adults to regulate tail regeneration. Here we report that Smo knockout embryonic NSCs oppose cartilage formation when engrafted to adult ETs, representing an important milestone in the creation of regenerated lizard tails with dorsoventrally patterned skeletal tissues. Nature Publishing Group UK 2021-10-14 /pmc/articles/PMC8516916/ /pubmed/34650077 http://dx.doi.org/10.1038/s41467-021-26321-9 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lozito, Thomas P. Londono, Ricardo Sun, Aaron X. Hudnall, Megan L. Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title | Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title_full | Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title_fullStr | Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title_full_unstemmed | Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title_short | Introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
title_sort | introducing dorsoventral patterning in adult regenerating lizard tails with gene-edited embryonic neural stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516916/ https://www.ncbi.nlm.nih.gov/pubmed/34650077 http://dx.doi.org/10.1038/s41467-021-26321-9 |
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