Identification of mechanosensitive genes during embryonic bone formation.

Although it is known that mechanical forces are needed for normal bone development, the current understanding of how biophysical stimuli are interpreted by and integrated with genetic regulatory mechanisms is limited. Mechanical forces are thought to be mediated in cells by "mechanosensitive&qu...

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Main Authors: Niamh C Nowlan, Patrick J Prendergast, Paula Murphy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-12-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC2592698?pdf=render
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spelling doaj-70b062d7becf4e31b38b024bf482015b2020-11-25T01:46:02ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582008-12-01412e100025010.1371/journal.pcbi.1000250Identification of mechanosensitive genes during embryonic bone formation.Niamh C NowlanPatrick J PrendergastPaula MurphyAlthough it is known that mechanical forces are needed for normal bone development, the current understanding of how biophysical stimuli are interpreted by and integrated with genetic regulatory mechanisms is limited. Mechanical forces are thought to be mediated in cells by "mechanosensitive" genes, but it is a challenge to demonstrate that the genetic regulation of the biological system is dependant on particular mechanical forces in vivo. We propose a new means of selecting candidate mechanosensitive genes by comparing in vivo gene expression patterns with patterns of biophysical stimuli, computed using finite element analysis. In this study, finite element analyses of the avian embryonic limb were performed using anatomically realistic rudiment and muscle morphologies, and patterns of biophysical stimuli were compared with the expression patterns of four candidate mechanosensitive genes integral to bone development. The expression patterns of two genes, Collagen X (ColX) and Indian hedgehog (Ihh), were shown to colocalise with biophysical stimuli induced by embryonic muscle contractions, identifying them as potentially being involved in the mechanoregulation of bone formation. An altered mechanical environment was induced in the embryonic chick, where a neuromuscular blocking agent was administered in ovo to modify skeletal muscle contractions. Finite element analyses predicted dramatic changes in levels and patterns of biophysical stimuli, and a number of immobilised specimens exhibited differences in ColX and Ihh expression. The results obtained indicate that computationally derived patterns of biophysical stimuli can be used to inform a directed search for genes that may play a mechanoregulatory role in particular in vivo events or processes. Furthermore, the experimental data demonstrate that ColX and Ihh are involved in mechanoregulatory pathways and may be key mediators in translating information from the mechanical environment to the molecular regulation of bone formation in the embryo.http://europepmc.org/articles/PMC2592698?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Niamh C Nowlan
Patrick J Prendergast
Paula Murphy
spellingShingle Niamh C Nowlan
Patrick J Prendergast
Paula Murphy
Identification of mechanosensitive genes during embryonic bone formation.
PLoS Computational Biology
author_facet Niamh C Nowlan
Patrick J Prendergast
Paula Murphy
author_sort Niamh C Nowlan
title Identification of mechanosensitive genes during embryonic bone formation.
title_short Identification of mechanosensitive genes during embryonic bone formation.
title_full Identification of mechanosensitive genes during embryonic bone formation.
title_fullStr Identification of mechanosensitive genes during embryonic bone formation.
title_full_unstemmed Identification of mechanosensitive genes during embryonic bone formation.
title_sort identification of mechanosensitive genes during embryonic bone formation.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2008-12-01
description Although it is known that mechanical forces are needed for normal bone development, the current understanding of how biophysical stimuli are interpreted by and integrated with genetic regulatory mechanisms is limited. Mechanical forces are thought to be mediated in cells by "mechanosensitive" genes, but it is a challenge to demonstrate that the genetic regulation of the biological system is dependant on particular mechanical forces in vivo. We propose a new means of selecting candidate mechanosensitive genes by comparing in vivo gene expression patterns with patterns of biophysical stimuli, computed using finite element analysis. In this study, finite element analyses of the avian embryonic limb were performed using anatomically realistic rudiment and muscle morphologies, and patterns of biophysical stimuli were compared with the expression patterns of four candidate mechanosensitive genes integral to bone development. The expression patterns of two genes, Collagen X (ColX) and Indian hedgehog (Ihh), were shown to colocalise with biophysical stimuli induced by embryonic muscle contractions, identifying them as potentially being involved in the mechanoregulation of bone formation. An altered mechanical environment was induced in the embryonic chick, where a neuromuscular blocking agent was administered in ovo to modify skeletal muscle contractions. Finite element analyses predicted dramatic changes in levels and patterns of biophysical stimuli, and a number of immobilised specimens exhibited differences in ColX and Ihh expression. The results obtained indicate that computationally derived patterns of biophysical stimuli can be used to inform a directed search for genes that may play a mechanoregulatory role in particular in vivo events or processes. Furthermore, the experimental data demonstrate that ColX and Ihh are involved in mechanoregulatory pathways and may be key mediators in translating information from the mechanical environment to the molecular regulation of bone formation in the embryo.
url http://europepmc.org/articles/PMC2592698?pdf=render
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AT patrickjprendergast identificationofmechanosensitivegenesduringembryonicboneformation
AT paulamurphy identificationofmechanosensitivegenesduringembryonicboneformation
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