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Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration

Postnatal tissue quiescence is thought to be a default state in the absence of a proliferative stimulus such as injury. Previous studies have demonstrated that certain embryonic development programs are reactivated aberrantly in adult organs to drive repair and regeneration(1–3), it is not well unde...

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Autores principales: Peng, Tien, Frank, David B., Kadzik, Rachel S., Morley, Michael P., Rathi, Komal S., Wang, Tao, Zhou, Su, Cheng, Lan, Lu, Min Min, Morrisey, Edward E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713039/
https://www.ncbi.nlm.nih.gov/pubmed/26436454
http://dx.doi.org/10.1038/nature14984
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author Peng, Tien
Frank, David B.
Kadzik, Rachel S.
Morley, Michael P.
Rathi, Komal S.
Wang, Tao
Zhou, Su
Cheng, Lan
Lu, Min Min
Morrisey, Edward E.
author_facet Peng, Tien
Frank, David B.
Kadzik, Rachel S.
Morley, Michael P.
Rathi, Komal S.
Wang, Tao
Zhou, Su
Cheng, Lan
Lu, Min Min
Morrisey, Edward E.
author_sort Peng, Tien
collection PubMed
description Postnatal tissue quiescence is thought to be a default state in the absence of a proliferative stimulus such as injury. Previous studies have demonstrated that certain embryonic development programs are reactivated aberrantly in adult organs to drive repair and regeneration(1–3), it is not well understood how quiescence is maintained in organs such as the lung which displays a remarkably low level of cellular turnover(4,5). We now demonstrate that quiescence in the adult lung is an actively maintained state and is regulated by hedgehog signaling. Epithelial-specific deletion of sonic hedgehog during postnatal homeostasis in the lung results in a proliferative expansion of the adjacent lung mesenchyme. Hedgehog signaling is initially down-regulated during the acute phase of epithelial injury as the mesenchyme proliferates in response, but returns to baseline during injury resolution as quiescence is restored. Activation of hedgehog during acute epithelial injury attenuates the proliferative expansion of the lung mesenchyme, whereas inactivation of hedgehog signaling prevents the restoration of quiescence during injury resolution. Finally, we show that hedgehog also regulates epithelial quiescence and regeneration in response to injury via a mesenchymal feedback mechanism. These results demonstrate that epithelial-mesenchymal interactions coordinated by hedgehog actively maintains postnatal tissue homeostasis, and deregulation of hedgehog during injury leads to aberrant repair and regeneration in the lung.
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spelling pubmed-47130392016-04-22 Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration Peng, Tien Frank, David B. Kadzik, Rachel S. Morley, Michael P. Rathi, Komal S. Wang, Tao Zhou, Su Cheng, Lan Lu, Min Min Morrisey, Edward E. Nature Article Postnatal tissue quiescence is thought to be a default state in the absence of a proliferative stimulus such as injury. Previous studies have demonstrated that certain embryonic development programs are reactivated aberrantly in adult organs to drive repair and regeneration(1–3), it is not well understood how quiescence is maintained in organs such as the lung which displays a remarkably low level of cellular turnover(4,5). We now demonstrate that quiescence in the adult lung is an actively maintained state and is regulated by hedgehog signaling. Epithelial-specific deletion of sonic hedgehog during postnatal homeostasis in the lung results in a proliferative expansion of the adjacent lung mesenchyme. Hedgehog signaling is initially down-regulated during the acute phase of epithelial injury as the mesenchyme proliferates in response, but returns to baseline during injury resolution as quiescence is restored. Activation of hedgehog during acute epithelial injury attenuates the proliferative expansion of the lung mesenchyme, whereas inactivation of hedgehog signaling prevents the restoration of quiescence during injury resolution. Finally, we show that hedgehog also regulates epithelial quiescence and regeneration in response to injury via a mesenchymal feedback mechanism. These results demonstrate that epithelial-mesenchymal interactions coordinated by hedgehog actively maintains postnatal tissue homeostasis, and deregulation of hedgehog during injury leads to aberrant repair and regeneration in the lung. 2015-10-05 2015-10-22 /pmc/articles/PMC4713039/ /pubmed/26436454 http://dx.doi.org/10.1038/nature14984 Text en Reprints and permission information is available at www.nature.com/reprints.
spellingShingle Article
Peng, Tien
Frank, David B.
Kadzik, Rachel S.
Morley, Michael P.
Rathi, Komal S.
Wang, Tao
Zhou, Su
Cheng, Lan
Lu, Min Min
Morrisey, Edward E.
Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title_full Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title_fullStr Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title_full_unstemmed Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title_short Hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
title_sort hedgehog actively maintains adult lung quiescence and regulates repair and regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713039/
https://www.ncbi.nlm.nih.gov/pubmed/26436454
http://dx.doi.org/10.1038/nature14984
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