Cargando…

Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration

Axolotls are uniquely able to resolve spinal cord injuries, but little is known about the mechanisms underlying spinal cord regeneration. We previously found that tail amputation leads to reactivation of a developmental-like program in spinal cord ependymal cells (Rodrigo Albors et al., 2015), chara...

Descripción completa

Detalles Bibliográficos
Autores principales: Cura Costa, Emanuel, Otsuki, Leo, Rodrigo Albors, Aida, Tanaka, Elly M, Chara, Osvaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205487/
https://www.ncbi.nlm.nih.gov/pubmed/33988504
http://dx.doi.org/10.7554/eLife.55665
_version_ 1783708515712368640
author Cura Costa, Emanuel
Otsuki, Leo
Rodrigo Albors, Aida
Tanaka, Elly M
Chara, Osvaldo
author_facet Cura Costa, Emanuel
Otsuki, Leo
Rodrigo Albors, Aida
Tanaka, Elly M
Chara, Osvaldo
author_sort Cura Costa, Emanuel
collection PubMed
description Axolotls are uniquely able to resolve spinal cord injuries, but little is known about the mechanisms underlying spinal cord regeneration. We previously found that tail amputation leads to reactivation of a developmental-like program in spinal cord ependymal cells (Rodrigo Albors et al., 2015), characterized by a high-proliferation zone emerging 4 days post-amputation (Rost et al., 2016). What underlies this spatiotemporal pattern of cell proliferation, however, remained unknown. Here, we use modeling, tightly linked to experimental data, to demonstrate that this regenerative response is consistent with a signal that recruits ependymal cells during ~85 hours after amputation within ~830 μm of the injury. We adapted Fluorescent Ubiquitination-based Cell Cycle Indicator (FUCCI) technology to axolotls (AxFUCCI) to visualize cell cycles in vivo. AxFUCCI axolotls confirmed the predicted appearance time and size of the injury-induced recruitment zone and revealed cell cycle synchrony between ependymal cells. Our modeling and imaging move us closer to understanding bona fide spinal cord regeneration.
format Online
Article
Text
id pubmed-8205487
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-82054872021-06-16 Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration Cura Costa, Emanuel Otsuki, Leo Rodrigo Albors, Aida Tanaka, Elly M Chara, Osvaldo eLife Computational and Systems Biology Axolotls are uniquely able to resolve spinal cord injuries, but little is known about the mechanisms underlying spinal cord regeneration. We previously found that tail amputation leads to reactivation of a developmental-like program in spinal cord ependymal cells (Rodrigo Albors et al., 2015), characterized by a high-proliferation zone emerging 4 days post-amputation (Rost et al., 2016). What underlies this spatiotemporal pattern of cell proliferation, however, remained unknown. Here, we use modeling, tightly linked to experimental data, to demonstrate that this regenerative response is consistent with a signal that recruits ependymal cells during ~85 hours after amputation within ~830 μm of the injury. We adapted Fluorescent Ubiquitination-based Cell Cycle Indicator (FUCCI) technology to axolotls (AxFUCCI) to visualize cell cycles in vivo. AxFUCCI axolotls confirmed the predicted appearance time and size of the injury-induced recruitment zone and revealed cell cycle synchrony between ependymal cells. Our modeling and imaging move us closer to understanding bona fide spinal cord regeneration. eLife Sciences Publications, Ltd 2021-05-14 /pmc/articles/PMC8205487/ /pubmed/33988504 http://dx.doi.org/10.7554/eLife.55665 Text en © 2021, Cura Costa et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Cura Costa, Emanuel
Otsuki, Leo
Rodrigo Albors, Aida
Tanaka, Elly M
Chara, Osvaldo
Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title_full Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title_fullStr Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title_full_unstemmed Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title_short Spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
title_sort spatiotemporal control of cell cycle acceleration during axolotl spinal cord regeneration
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205487/
https://www.ncbi.nlm.nih.gov/pubmed/33988504
http://dx.doi.org/10.7554/eLife.55665
work_keys_str_mv AT curacostaemanuel spatiotemporalcontrolofcellcycleaccelerationduringaxolotlspinalcordregeneration
AT otsukileo spatiotemporalcontrolofcellcycleaccelerationduringaxolotlspinalcordregeneration
AT rodrigoalborsaida spatiotemporalcontrolofcellcycleaccelerationduringaxolotlspinalcordregeneration
AT tanakaellym spatiotemporalcontrolofcellcycleaccelerationduringaxolotlspinalcordregeneration
AT charaosvaldo spatiotemporalcontrolofcellcycleaccelerationduringaxolotlspinalcordregeneration