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Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures
Models of bone remodelling could be useful in drug discovery, particularly if the model is one that replicates bone regeneration with reduction in osteoclast activity. Here we use nanovibrational stimulation to achieve this in a 3D co-culture of primary human osteoprogenitor and osteoclast progenito...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611084/ https://www.ncbi.nlm.nih.gov/pubmed/34815449 http://dx.doi.org/10.1038/s41598-021-02139-9 |
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author | Kennedy, John W. Tsimbouri, P. Monica Campsie, Paul Sood, Shatakshi Childs, Peter G. Reid, Stuart Young, Peter S. Meek, Dominic R. M. Goodyear, Carl S. Dalby, Matthew J. |
author_facet | Kennedy, John W. Tsimbouri, P. Monica Campsie, Paul Sood, Shatakshi Childs, Peter G. Reid, Stuart Young, Peter S. Meek, Dominic R. M. Goodyear, Carl S. Dalby, Matthew J. |
author_sort | Kennedy, John W. |
collection | PubMed |
description | Models of bone remodelling could be useful in drug discovery, particularly if the model is one that replicates bone regeneration with reduction in osteoclast activity. Here we use nanovibrational stimulation to achieve this in a 3D co-culture of primary human osteoprogenitor and osteoclast progenitor cells. We show that 1000 Hz frequency, 40 nm amplitude vibration reduces osteoclast formation and activity in human mononuclear CD14(+) blood cells. Additionally, this nanoscale vibration both enhances osteogenesis and reduces osteoclastogenesis in a co-culture of primary human bone marrow stromal cells and bone marrow hematopoietic cells. Further, we use metabolomics to identify Akt (protein kinase C) as a potential mediator. Akt is known to be involved in bone differentiation via transforming growth factor beta 1 (TGFβ1) and bone morphogenetic protein 2 (BMP2) and it has been implicated in reduced osteoclast activity via Guanine nucleotide-binding protein subunit α13 (Gα13). With further validation, our nanovibrational bioreactor could be used to help provide humanised 3D models for drug screening. |
format | Online Article Text |
id | pubmed-8611084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86110842021-11-26 Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures Kennedy, John W. Tsimbouri, P. Monica Campsie, Paul Sood, Shatakshi Childs, Peter G. Reid, Stuart Young, Peter S. Meek, Dominic R. M. Goodyear, Carl S. Dalby, Matthew J. Sci Rep Article Models of bone remodelling could be useful in drug discovery, particularly if the model is one that replicates bone regeneration with reduction in osteoclast activity. Here we use nanovibrational stimulation to achieve this in a 3D co-culture of primary human osteoprogenitor and osteoclast progenitor cells. We show that 1000 Hz frequency, 40 nm amplitude vibration reduces osteoclast formation and activity in human mononuclear CD14(+) blood cells. Additionally, this nanoscale vibration both enhances osteogenesis and reduces osteoclastogenesis in a co-culture of primary human bone marrow stromal cells and bone marrow hematopoietic cells. Further, we use metabolomics to identify Akt (protein kinase C) as a potential mediator. Akt is known to be involved in bone differentiation via transforming growth factor beta 1 (TGFβ1) and bone morphogenetic protein 2 (BMP2) and it has been implicated in reduced osteoclast activity via Guanine nucleotide-binding protein subunit α13 (Gα13). With further validation, our nanovibrational bioreactor could be used to help provide humanised 3D models for drug screening. Nature Publishing Group UK 2021-11-23 /pmc/articles/PMC8611084/ /pubmed/34815449 http://dx.doi.org/10.1038/s41598-021-02139-9 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kennedy, John W. Tsimbouri, P. Monica Campsie, Paul Sood, Shatakshi Childs, Peter G. Reid, Stuart Young, Peter S. Meek, Dominic R. M. Goodyear, Carl S. Dalby, Matthew J. Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title | Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title_full | Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title_fullStr | Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title_full_unstemmed | Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title_short | Nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
title_sort | nanovibrational stimulation inhibits osteoclastogenesis and enhances osteogenesis in co-cultures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611084/ https://www.ncbi.nlm.nih.gov/pubmed/34815449 http://dx.doi.org/10.1038/s41598-021-02139-9 |
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