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Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice
Catch-up growth after insults to growing organs is paramount to achieving robust body proportions. In fly larvae, injury to individual tissues is followed by local and systemic compensatory mechanisms that allow the damaged tissue to regain normal proportions with other tissues. In vertebrates, loca...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019387/ https://www.ncbi.nlm.nih.gov/pubmed/29944650 http://dx.doi.org/10.1371/journal.pbio.2005086 |
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author | Roselló-Díez, Alberto Madisen, Linda Bastide, Sébastien Zeng, Hongkui Joyner, Alexandra L. |
author_facet | Roselló-Díez, Alberto Madisen, Linda Bastide, Sébastien Zeng, Hongkui Joyner, Alexandra L. |
author_sort | Roselló-Díez, Alberto |
collection | PubMed |
description | Catch-up growth after insults to growing organs is paramount to achieving robust body proportions. In fly larvae, injury to individual tissues is followed by local and systemic compensatory mechanisms that allow the damaged tissue to regain normal proportions with other tissues. In vertebrates, local catch-up growth has been described after transient reduction of bone growth, but the underlying cellular responses are controversial. We developed an approach to study catch-up growth in foetal mice in which mosaic expression of the cell cycle suppressor p21 is induced in the cartilage cells (chondrocytes) that drive long-bone elongation. By specifically targeting p21 expression to left hindlimb chondrocytes, the right limb serves as an internal control. Unexpectedly, left–right limb symmetry remained normal, revealing deployment of compensatory mechanisms. Above a certain threshold of insult, an orchestrated response was triggered involving local enhancement of bone growth and systemic growth reduction that ensured that body proportions were maintained. The local response entailed hyperproliferation of spared left limb chondrocytes that was associated with reduced chondrocyte density. The systemic effect involved impaired placental function and IGF signalling, revealing bone–placenta communication. Therefore, vertebrates, like invertebrates, can mount coordinated local and systemic responses to developmental insults that ensure that normal body proportions are maintained. |
format | Online Article Text |
id | pubmed-6019387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60193872018-07-07 Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice Roselló-Díez, Alberto Madisen, Linda Bastide, Sébastien Zeng, Hongkui Joyner, Alexandra L. PLoS Biol Research Article Catch-up growth after insults to growing organs is paramount to achieving robust body proportions. In fly larvae, injury to individual tissues is followed by local and systemic compensatory mechanisms that allow the damaged tissue to regain normal proportions with other tissues. In vertebrates, local catch-up growth has been described after transient reduction of bone growth, but the underlying cellular responses are controversial. We developed an approach to study catch-up growth in foetal mice in which mosaic expression of the cell cycle suppressor p21 is induced in the cartilage cells (chondrocytes) that drive long-bone elongation. By specifically targeting p21 expression to left hindlimb chondrocytes, the right limb serves as an internal control. Unexpectedly, left–right limb symmetry remained normal, revealing deployment of compensatory mechanisms. Above a certain threshold of insult, an orchestrated response was triggered involving local enhancement of bone growth and systemic growth reduction that ensured that body proportions were maintained. The local response entailed hyperproliferation of spared left limb chondrocytes that was associated with reduced chondrocyte density. The systemic effect involved impaired placental function and IGF signalling, revealing bone–placenta communication. Therefore, vertebrates, like invertebrates, can mount coordinated local and systemic responses to developmental insults that ensure that normal body proportions are maintained. Public Library of Science 2018-06-26 /pmc/articles/PMC6019387/ /pubmed/29944650 http://dx.doi.org/10.1371/journal.pbio.2005086 Text en © 2018 Roselló-Díez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Roselló-Díez, Alberto Madisen, Linda Bastide, Sébastien Zeng, Hongkui Joyner, Alexandra L. Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title | Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title_full | Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title_fullStr | Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title_full_unstemmed | Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title_short | Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
title_sort | cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019387/ https://www.ncbi.nlm.nih.gov/pubmed/29944650 http://dx.doi.org/10.1371/journal.pbio.2005086 |
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