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Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts

Bone turnover in vivo is regulated by mechanical forces such as shear stress originating from interstitial oscillatory fluid flow (OFF), and bone cells in vitro respond to mechanical loading. However, the mechanisms by which bone cells sense mechanical forces, resulting in increased mineral depositi...

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Autores principales: Delaine-Smith, Robin M., Sittichokechaiwut, Anuphan, Reilly, Gwendolen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4012163/
https://www.ncbi.nlm.nih.gov/pubmed/24097311
http://dx.doi.org/10.1096/fj.13-231894
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author Delaine-Smith, Robin M.
Sittichokechaiwut, Anuphan
Reilly, Gwendolen C.
author_facet Delaine-Smith, Robin M.
Sittichokechaiwut, Anuphan
Reilly, Gwendolen C.
author_sort Delaine-Smith, Robin M.
collection PubMed
description Bone turnover in vivo is regulated by mechanical forces such as shear stress originating from interstitial oscillatory fluid flow (OFF), and bone cells in vitro respond to mechanical loading. However, the mechanisms by which bone cells sense mechanical forces, resulting in increased mineral deposition, are not well understood. The aim of this study was to investigate the role of the primary cilium in mechanosensing by osteoblasts. MLO-A5 murine osteoblasts were cultured in monolayer and subjected to two different OFF regimens: 5 short (2 h daily) bouts of OFF followed by morphological analysis of primary cilia; or exposure to chloral hydrate to damage or remove primary cilia and 2 short bouts (2 h on consecutive days) of OFF. Primary cilia were shorter and there were fewer cilia per cell after exposure to periods of OFF compared with static controls. Damage or removal of primary cilia inhibited OFF-induced PGE(2) release into the medium and mineral deposition, assayed by Alizarin red staining. We conclude that primary cilia are important mediators of OFF-induced mineral deposition, which has relevance for the design of bone tissue engineering strategies and may inform clinical treatments of bone disorders causes by load-deficiency.—Delaine-Smith, R. M., Sittichokechaiwut, A., Reilly, G. C. Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts.
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spelling pubmed-40121632014-05-22 Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts Delaine-Smith, Robin M. Sittichokechaiwut, Anuphan Reilly, Gwendolen C. FASEB J Research Communications Bone turnover in vivo is regulated by mechanical forces such as shear stress originating from interstitial oscillatory fluid flow (OFF), and bone cells in vitro respond to mechanical loading. However, the mechanisms by which bone cells sense mechanical forces, resulting in increased mineral deposition, are not well understood. The aim of this study was to investigate the role of the primary cilium in mechanosensing by osteoblasts. MLO-A5 murine osteoblasts were cultured in monolayer and subjected to two different OFF regimens: 5 short (2 h daily) bouts of OFF followed by morphological analysis of primary cilia; or exposure to chloral hydrate to damage or remove primary cilia and 2 short bouts (2 h on consecutive days) of OFF. Primary cilia were shorter and there were fewer cilia per cell after exposure to periods of OFF compared with static controls. Damage or removal of primary cilia inhibited OFF-induced PGE(2) release into the medium and mineral deposition, assayed by Alizarin red staining. We conclude that primary cilia are important mediators of OFF-induced mineral deposition, which has relevance for the design of bone tissue engineering strategies and may inform clinical treatments of bone disorders causes by load-deficiency.—Delaine-Smith, R. M., Sittichokechaiwut, A., Reilly, G. C. Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts. Federation of American Societies for Experimental Biology 2014-01 /pmc/articles/PMC4012163/ /pubmed/24097311 http://dx.doi.org/10.1096/fj.13-231894 Text en © FASEB This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported (CC BY 3.0) (http://creativecommons.org/licenses/by/3.0/deed.en_US) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Communications
Delaine-Smith, Robin M.
Sittichokechaiwut, Anuphan
Reilly, Gwendolen C.
Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title_full Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title_fullStr Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title_full_unstemmed Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title_short Primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
title_sort primary cilia respond to fluid shear stress and mediate flow-induced calcium deposition in osteoblasts
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4012163/
https://www.ncbi.nlm.nih.gov/pubmed/24097311
http://dx.doi.org/10.1096/fj.13-231894
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