Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782314894573436928 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4012163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Federation of American Societies for Experimental Biology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT delainesmithrobinm primaryciliarespondtofluidshearstressandmediateflowinducedcalciumdepositioninosteoblasts AT sittichokechaiwutanuphan primaryciliarespondtofluidshearstressandmediateflowinducedcalciumdepositioninosteoblasts AT reillygwendolenc primaryciliarespondtofluidshearstressandmediateflowinducedcalciumdepositioninosteoblasts |