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A distinct transition from cell growth to physiological homeostasis in the tendon

Changes in cell proliferation define transitions from tissue growth to physiological homeostasis. In tendons, a highly organized extracellular matrix undergoes significant postnatal expansion to drive growth, but once formed, it appears to undergo little turnover. However, tendon cell activity durin...

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Detalles Bibliográficos
Autores principales: Grinstein, Mor, Dingwall, Heather L, O'Connor, Luke D, Zou, Ken, Capellini, Terence Dante, Galloway, Jenna Lauren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791717/
https://www.ncbi.nlm.nih.gov/pubmed/31535975
http://dx.doi.org/10.7554/eLife.48689
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author Grinstein, Mor
Dingwall, Heather L
O'Connor, Luke D
Zou, Ken
Capellini, Terence Dante
Galloway, Jenna Lauren
author_facet Grinstein, Mor
Dingwall, Heather L
O'Connor, Luke D
Zou, Ken
Capellini, Terence Dante
Galloway, Jenna Lauren
author_sort Grinstein, Mor
collection PubMed
description Changes in cell proliferation define transitions from tissue growth to physiological homeostasis. In tendons, a highly organized extracellular matrix undergoes significant postnatal expansion to drive growth, but once formed, it appears to undergo little turnover. However, tendon cell activity during growth and homeostatic maintenance is less well defined. Using complementary methods of genetic H2B-GFP pulse-chase labeling and BrdU incorporation in mice, we show significant postnatal tendon cell proliferation, correlating with longitudinal Achilles tendon growth. Around day 21, there is a transition in cell turnover with a significant decline in proliferation. After this time, we find low amounts of homeostatic tendon cell proliferation from 3 to 20 months. These results demonstrate that tendons harbor significant postnatal mitotic activity, and limited, but detectable activity in adult and aged stages. It also points towards the possibility that the adult tendon harbors resident tendon progenitor populations, which would have important therapeutic implications.
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spelling pubmed-67917172019-10-16 A distinct transition from cell growth to physiological homeostasis in the tendon Grinstein, Mor Dingwall, Heather L O'Connor, Luke D Zou, Ken Capellini, Terence Dante Galloway, Jenna Lauren eLife Developmental Biology Changes in cell proliferation define transitions from tissue growth to physiological homeostasis. In tendons, a highly organized extracellular matrix undergoes significant postnatal expansion to drive growth, but once formed, it appears to undergo little turnover. However, tendon cell activity during growth and homeostatic maintenance is less well defined. Using complementary methods of genetic H2B-GFP pulse-chase labeling and BrdU incorporation in mice, we show significant postnatal tendon cell proliferation, correlating with longitudinal Achilles tendon growth. Around day 21, there is a transition in cell turnover with a significant decline in proliferation. After this time, we find low amounts of homeostatic tendon cell proliferation from 3 to 20 months. These results demonstrate that tendons harbor significant postnatal mitotic activity, and limited, but detectable activity in adult and aged stages. It also points towards the possibility that the adult tendon harbors resident tendon progenitor populations, which would have important therapeutic implications. eLife Sciences Publications, Ltd 2019-09-19 /pmc/articles/PMC6791717/ /pubmed/31535975 http://dx.doi.org/10.7554/eLife.48689 Text en © 2019, Grinstein et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Grinstein, Mor
Dingwall, Heather L
O'Connor, Luke D
Zou, Ken
Capellini, Terence Dante
Galloway, Jenna Lauren
A distinct transition from cell growth to physiological homeostasis in the tendon
title A distinct transition from cell growth to physiological homeostasis in the tendon
title_full A distinct transition from cell growth to physiological homeostasis in the tendon
title_fullStr A distinct transition from cell growth to physiological homeostasis in the tendon
title_full_unstemmed A distinct transition from cell growth to physiological homeostasis in the tendon
title_short A distinct transition from cell growth to physiological homeostasis in the tendon
title_sort distinct transition from cell growth to physiological homeostasis in the tendon
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791717/
https://www.ncbi.nlm.nih.gov/pubmed/31535975
http://dx.doi.org/10.7554/eLife.48689
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