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Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles

Bone formation or regeneration requires the recruitment, proliferation, and osteogenic differentiation of stem/stromal progenitor cells. A potent stimulus driving this process is mechanical loading. Osteocytes are mechanosensitive cells that play fundamental roles in coordinating loading‐induced bon...

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Autores principales: Eichholz, Kian F., Woods, Ian, Riffault, Mathieu, Johnson, Gillian P., Corrigan, Michele, Lowry, Michelle C., Shen, Nian, Labour, Marie‐Noelle, Wynne, Kieran, O'Driscoll, Lorraine, Hoey, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581449/
https://www.ncbi.nlm.nih.gov/pubmed/32672416
http://dx.doi.org/10.1002/sctm.19-0405
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author Eichholz, Kian F.
Woods, Ian
Riffault, Mathieu
Johnson, Gillian P.
Corrigan, Michele
Lowry, Michelle C.
Shen, Nian
Labour, Marie‐Noelle
Wynne, Kieran
O'Driscoll, Lorraine
Hoey, David A.
author_facet Eichholz, Kian F.
Woods, Ian
Riffault, Mathieu
Johnson, Gillian P.
Corrigan, Michele
Lowry, Michelle C.
Shen, Nian
Labour, Marie‐Noelle
Wynne, Kieran
O'Driscoll, Lorraine
Hoey, David A.
author_sort Eichholz, Kian F.
collection PubMed
description Bone formation or regeneration requires the recruitment, proliferation, and osteogenic differentiation of stem/stromal progenitor cells. A potent stimulus driving this process is mechanical loading. Osteocytes are mechanosensitive cells that play fundamental roles in coordinating loading‐induced bone formation via the secretion of paracrine factors. However, the exact mechanisms by which osteocytes relay mechanical signals to these progenitor cells are poorly understood. Therefore, this study aimed to demonstrate the potency of the mechanically stimulated osteocyte secretome in driving human bone marrow stem/stromal cell (hMSC) recruitment and differentiation, and characterize the secretome to identify potential factors regulating stem cell behavior and bone mechanobiology. We demonstrate that osteocytes subjected to fluid shear secrete a distinct collection of factors that significantly enhance hMSC recruitment and osteogenesis and demonstrate the key role of extracellular vesicles (EVs) in driving these effects. This demonstrates the pro‐osteogenic potential of osteocyte‐derived mechanically activated extracellular vesicles, which have great potential as a cell‐free therapy to enhance bone regeneration and repair in diseases such as osteoporosis.
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spelling pubmed-75814492020-10-27 Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles Eichholz, Kian F. Woods, Ian Riffault, Mathieu Johnson, Gillian P. Corrigan, Michele Lowry, Michelle C. Shen, Nian Labour, Marie‐Noelle Wynne, Kieran O'Driscoll, Lorraine Hoey, David A. Stem Cells Transl Med Tissue‐specific Progenitor and Stem Cells Bone formation or regeneration requires the recruitment, proliferation, and osteogenic differentiation of stem/stromal progenitor cells. A potent stimulus driving this process is mechanical loading. Osteocytes are mechanosensitive cells that play fundamental roles in coordinating loading‐induced bone formation via the secretion of paracrine factors. However, the exact mechanisms by which osteocytes relay mechanical signals to these progenitor cells are poorly understood. Therefore, this study aimed to demonstrate the potency of the mechanically stimulated osteocyte secretome in driving human bone marrow stem/stromal cell (hMSC) recruitment and differentiation, and characterize the secretome to identify potential factors regulating stem cell behavior and bone mechanobiology. We demonstrate that osteocytes subjected to fluid shear secrete a distinct collection of factors that significantly enhance hMSC recruitment and osteogenesis and demonstrate the key role of extracellular vesicles (EVs) in driving these effects. This demonstrates the pro‐osteogenic potential of osteocyte‐derived mechanically activated extracellular vesicles, which have great potential as a cell‐free therapy to enhance bone regeneration and repair in diseases such as osteoporosis. John Wiley & Sons, Inc. 2020-07-16 /pmc/articles/PMC7581449/ /pubmed/32672416 http://dx.doi.org/10.1002/sctm.19-0405 Text en © 2020 The Authors. stem cells translational medicine published by Wiley Periodicals LLC on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Tissue‐specific Progenitor and Stem Cells
Eichholz, Kian F.
Woods, Ian
Riffault, Mathieu
Johnson, Gillian P.
Corrigan, Michele
Lowry, Michelle C.
Shen, Nian
Labour, Marie‐Noelle
Wynne, Kieran
O'Driscoll, Lorraine
Hoey, David A.
Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title_full Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title_fullStr Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title_full_unstemmed Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title_short Human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
title_sort human bone marrow stem/stromal cell osteogenesis is regulated via mechanically activated osteocyte‐derived extracellular vesicles
topic Tissue‐specific Progenitor and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581449/
https://www.ncbi.nlm.nih.gov/pubmed/32672416
http://dx.doi.org/10.1002/sctm.19-0405
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