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CD59 mediates cartilage patterning during spontaneous tail regeneration
The regeneration-competent adult animals have ability to regenerate their lost complex appendages with a near-perfect replica, owing to the positional identity acquired by the progenitor cells in the blastema, i.e. the blastemal cells. CD59, a CD59/Ly6 family member, has been identified as a regulat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523838/ https://www.ncbi.nlm.nih.gov/pubmed/26238652 http://dx.doi.org/10.1038/srep12798 |
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author | Bai, Xue Wang, Yingjie Man, Lili Zhang, Qing Sun, Cheng Hu, Wen Liu, Yan Liu, Mei Gu, Xiaosong Wang, Yongjun |
author_facet | Bai, Xue Wang, Yingjie Man, Lili Zhang, Qing Sun, Cheng Hu, Wen Liu, Yan Liu, Mei Gu, Xiaosong Wang, Yongjun |
author_sort | Bai, Xue |
collection | PubMed |
description | The regeneration-competent adult animals have ability to regenerate their lost complex appendages with a near-perfect replica, owing to the positional identity acquired by the progenitor cells in the blastema, i.e. the blastemal cells. CD59, a CD59/Ly6 family member, has been identified as a regulator of positional identity in the tail blastemal cells of Gekko japonicus. To determine whether this function of CD59 is unique to the regenerative amniote(s) and how CD59 mediates PD axis patterning during tail regeneration, we examined its protective role on the complement-mediated cell lysis and intervened CD59 expression in the tail blastemal cells using an in vivo model of adenovirus transfection. Our data revealed that gecko CD59 was able to inhibit complement-mediated cell lysis. Meanwhile, CD59 functioned on positional identity through expression in cartilage precursor cells. Intervening positional identity by overexpression or siRNA knockdown of CD59 resulted in abnormal cartilaginous cone patterning due to the decreased differentiation of blastemal cells to cartilage precursor cells. The cartilage formation-related genes were found to be under the regulation of CD59. These results indicate that CD59, an evolutionarily transitional molecule linking immune and regenerative regulation, affects tail regeneration by mediating cartilage patterning. |
format | Online Article Text |
id | pubmed-4523838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45238382015-08-05 CD59 mediates cartilage patterning during spontaneous tail regeneration Bai, Xue Wang, Yingjie Man, Lili Zhang, Qing Sun, Cheng Hu, Wen Liu, Yan Liu, Mei Gu, Xiaosong Wang, Yongjun Sci Rep Article The regeneration-competent adult animals have ability to regenerate their lost complex appendages with a near-perfect replica, owing to the positional identity acquired by the progenitor cells in the blastema, i.e. the blastemal cells. CD59, a CD59/Ly6 family member, has been identified as a regulator of positional identity in the tail blastemal cells of Gekko japonicus. To determine whether this function of CD59 is unique to the regenerative amniote(s) and how CD59 mediates PD axis patterning during tail regeneration, we examined its protective role on the complement-mediated cell lysis and intervened CD59 expression in the tail blastemal cells using an in vivo model of adenovirus transfection. Our data revealed that gecko CD59 was able to inhibit complement-mediated cell lysis. Meanwhile, CD59 functioned on positional identity through expression in cartilage precursor cells. Intervening positional identity by overexpression or siRNA knockdown of CD59 resulted in abnormal cartilaginous cone patterning due to the decreased differentiation of blastemal cells to cartilage precursor cells. The cartilage formation-related genes were found to be under the regulation of CD59. These results indicate that CD59, an evolutionarily transitional molecule linking immune and regenerative regulation, affects tail regeneration by mediating cartilage patterning. Nature Publishing Group 2015-08-04 /pmc/articles/PMC4523838/ /pubmed/26238652 http://dx.doi.org/10.1038/srep12798 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bai, Xue Wang, Yingjie Man, Lili Zhang, Qing Sun, Cheng Hu, Wen Liu, Yan Liu, Mei Gu, Xiaosong Wang, Yongjun CD59 mediates cartilage patterning during spontaneous tail regeneration |
title | CD59 mediates cartilage patterning during spontaneous tail regeneration |
title_full | CD59 mediates cartilage patterning during spontaneous tail regeneration |
title_fullStr | CD59 mediates cartilage patterning during spontaneous tail regeneration |
title_full_unstemmed | CD59 mediates cartilage patterning during spontaneous tail regeneration |
title_short | CD59 mediates cartilage patterning during spontaneous tail regeneration |
title_sort | cd59 mediates cartilage patterning during spontaneous tail regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523838/ https://www.ncbi.nlm.nih.gov/pubmed/26238652 http://dx.doi.org/10.1038/srep12798 |
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