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On the horizon: Hedgehog signaling to heal broken bones
Uncovering the molecular pathways that drive skeletal repair has been an ongoing challenge. Initial efforts have relied on in vitro assays to identify the key signaling pathways that drive cartilage and bone differentiation. While these assays can provide some clues, assessing specific pathways in a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844053/ https://www.ncbi.nlm.nih.gov/pubmed/35165260 http://dx.doi.org/10.1038/s41413-021-00184-8 |
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author | Kuwahara, Stephanie T. Liu, Shuwan Chareunsouk, Andrew Serowoky, Maxwell Mariani, Francesca V. |
author_facet | Kuwahara, Stephanie T. Liu, Shuwan Chareunsouk, Andrew Serowoky, Maxwell Mariani, Francesca V. |
author_sort | Kuwahara, Stephanie T. |
collection | PubMed |
description | Uncovering the molecular pathways that drive skeletal repair has been an ongoing challenge. Initial efforts have relied on in vitro assays to identify the key signaling pathways that drive cartilage and bone differentiation. While these assays can provide some clues, assessing specific pathways in animal models is critical. Furthermore, definitive proof that a pathway is required for skeletal repair is best provided using genetic tests. Stimulating the Hh (Hedgehog) pathway can promote cartilage and bone differentiation in cell culture assays. In addition, the application of HH protein or various pathway agonists in vivo has a positive influence on bone healing. Until recently, however, genetic proof that the Hh pathway is involved in bone repair has been lacking. Here, we consider both in vitro and in vivo studies that examine the role of Hh in repair and discuss some of the challenges inherent in their interpretation. We also identify needed areas of study considering a new appreciation for the role of cartilage during repair, the variety of cell types that may have differing roles in repair, and the recent availability of powerful lineage tracing techniques. We are optimistic that emerging genetic tools will make it possible to precisely define when and in which cells promoting Hh signaling can best promote skeletal repair, and thus, the clinical potential for targeting the Hh pathway can be realized. |
format | Online Article Text |
id | pubmed-8844053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88440532022-03-02 On the horizon: Hedgehog signaling to heal broken bones Kuwahara, Stephanie T. Liu, Shuwan Chareunsouk, Andrew Serowoky, Maxwell Mariani, Francesca V. Bone Res Review Article Uncovering the molecular pathways that drive skeletal repair has been an ongoing challenge. Initial efforts have relied on in vitro assays to identify the key signaling pathways that drive cartilage and bone differentiation. While these assays can provide some clues, assessing specific pathways in animal models is critical. Furthermore, definitive proof that a pathway is required for skeletal repair is best provided using genetic tests. Stimulating the Hh (Hedgehog) pathway can promote cartilage and bone differentiation in cell culture assays. In addition, the application of HH protein or various pathway agonists in vivo has a positive influence on bone healing. Until recently, however, genetic proof that the Hh pathway is involved in bone repair has been lacking. Here, we consider both in vitro and in vivo studies that examine the role of Hh in repair and discuss some of the challenges inherent in their interpretation. We also identify needed areas of study considering a new appreciation for the role of cartilage during repair, the variety of cell types that may have differing roles in repair, and the recent availability of powerful lineage tracing techniques. We are optimistic that emerging genetic tools will make it possible to precisely define when and in which cells promoting Hh signaling can best promote skeletal repair, and thus, the clinical potential for targeting the Hh pathway can be realized. Nature Publishing Group UK 2022-02-15 /pmc/articles/PMC8844053/ /pubmed/35165260 http://dx.doi.org/10.1038/s41413-021-00184-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Kuwahara, Stephanie T. Liu, Shuwan Chareunsouk, Andrew Serowoky, Maxwell Mariani, Francesca V. On the horizon: Hedgehog signaling to heal broken bones |
title | On the horizon: Hedgehog signaling to heal broken bones |
title_full | On the horizon: Hedgehog signaling to heal broken bones |
title_fullStr | On the horizon: Hedgehog signaling to heal broken bones |
title_full_unstemmed | On the horizon: Hedgehog signaling to heal broken bones |
title_short | On the horizon: Hedgehog signaling to heal broken bones |
title_sort | on the horizon: hedgehog signaling to heal broken bones |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844053/ https://www.ncbi.nlm.nih.gov/pubmed/35165260 http://dx.doi.org/10.1038/s41413-021-00184-8 |
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