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Counteracting bone fragility with human amniotic mesenchymal stem cells
The impaired maturation of bone-forming osteoblasts results in reduced bone formation and subsequent bone weakening, which leads to a number of conditions such as osteogenesis imperfecta (OI). Transplantation of human fetal mesenchymal stem cells has been proposed as skeletal anabolic therapy to enh...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5171815/ https://www.ncbi.nlm.nih.gov/pubmed/27995994 http://dx.doi.org/10.1038/srep39656 |
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author | Ranzoni, Anna M. Corcelli, Michelangelo Hau, Kwan-Leong Kerns, Jemma G. Vanleene, Maximilien Shefelbine, Sandra Jones, Gemma N. Moschidou, Dafni Dala-Ali, Benan Goodship, Allen E. De Coppi, Paolo Arnett, Timothy R. Guillot, Pascale V. |
author_facet | Ranzoni, Anna M. Corcelli, Michelangelo Hau, Kwan-Leong Kerns, Jemma G. Vanleene, Maximilien Shefelbine, Sandra Jones, Gemma N. Moschidou, Dafni Dala-Ali, Benan Goodship, Allen E. De Coppi, Paolo Arnett, Timothy R. Guillot, Pascale V. |
author_sort | Ranzoni, Anna M. |
collection | PubMed |
description | The impaired maturation of bone-forming osteoblasts results in reduced bone formation and subsequent bone weakening, which leads to a number of conditions such as osteogenesis imperfecta (OI). Transplantation of human fetal mesenchymal stem cells has been proposed as skeletal anabolic therapy to enhance bone formation, but the mechanisms underlying the contribution of the donor cells to bone health are poorly understood and require further elucidation. Here, we show that intraperitoneal injection of human amniotic mesenchymal stem cells (AFSCs) into a mouse model of OI (oim mice) reduced fracture susceptibility, increased bone strength, improved bone quality and micro-architecture, normalised bone remodelling and reduced TNFα and TGFβ sigalling. Donor cells engrafted into bones and differentiated into osteoblasts but importantly, also promoted endogenous osteogenesis and the maturation of resident osteoblasts. Together, these findings identify AFSC transplantation as a countermeasure to bone fragility. These data have wider implications for bone health and fracture reduction. |
format | Online Article Text |
id | pubmed-5171815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51718152016-12-28 Counteracting bone fragility with human amniotic mesenchymal stem cells Ranzoni, Anna M. Corcelli, Michelangelo Hau, Kwan-Leong Kerns, Jemma G. Vanleene, Maximilien Shefelbine, Sandra Jones, Gemma N. Moschidou, Dafni Dala-Ali, Benan Goodship, Allen E. De Coppi, Paolo Arnett, Timothy R. Guillot, Pascale V. Sci Rep Article The impaired maturation of bone-forming osteoblasts results in reduced bone formation and subsequent bone weakening, which leads to a number of conditions such as osteogenesis imperfecta (OI). Transplantation of human fetal mesenchymal stem cells has been proposed as skeletal anabolic therapy to enhance bone formation, but the mechanisms underlying the contribution of the donor cells to bone health are poorly understood and require further elucidation. Here, we show that intraperitoneal injection of human amniotic mesenchymal stem cells (AFSCs) into a mouse model of OI (oim mice) reduced fracture susceptibility, increased bone strength, improved bone quality and micro-architecture, normalised bone remodelling and reduced TNFα and TGFβ sigalling. Donor cells engrafted into bones and differentiated into osteoblasts but importantly, also promoted endogenous osteogenesis and the maturation of resident osteoblasts. Together, these findings identify AFSC transplantation as a countermeasure to bone fragility. These data have wider implications for bone health and fracture reduction. Nature Publishing Group 2016-12-20 /pmc/articles/PMC5171815/ /pubmed/27995994 http://dx.doi.org/10.1038/srep39656 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ranzoni, Anna M. Corcelli, Michelangelo Hau, Kwan-Leong Kerns, Jemma G. Vanleene, Maximilien Shefelbine, Sandra Jones, Gemma N. Moschidou, Dafni Dala-Ali, Benan Goodship, Allen E. De Coppi, Paolo Arnett, Timothy R. Guillot, Pascale V. Counteracting bone fragility with human amniotic mesenchymal stem cells |
title | Counteracting bone fragility with human amniotic mesenchymal stem cells |
title_full | Counteracting bone fragility with human amniotic mesenchymal stem cells |
title_fullStr | Counteracting bone fragility with human amniotic mesenchymal stem cells |
title_full_unstemmed | Counteracting bone fragility with human amniotic mesenchymal stem cells |
title_short | Counteracting bone fragility with human amniotic mesenchymal stem cells |
title_sort | counteracting bone fragility with human amniotic mesenchymal stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5171815/ https://www.ncbi.nlm.nih.gov/pubmed/27995994 http://dx.doi.org/10.1038/srep39656 |
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