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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6791717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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