Literature DB >> 16456854

Genes, forces, and forms: mechanical aspects of prenatal craniofacial development.

Ralf J Radlanski1, Herbert Renz.   

Abstract

Current knowledge of molecular signaling during craniofacial development is advancing rapidly. We know that cells can respond to mechanical stimuli by biochemical signaling. Thus, the link between mechanical stimuli and gene expression has become a new and important area of the morphological sciences. This field of research seems to be a revival of the old approach of developmental mechanics, which goes back to the embryologists His (1874), Carey (1920), and Blechschmidt (1948). These researchers argued that forces play a fundamental role in tissue differentiation and morphogenesis. They understood morphogenesis as a closed system with living cells as the active part and biological, chemical, and physical laws as the rules. This review reports on linking mechanical aspects of developmental biology with the contemporary knowledge of tissue differentiation. We focus on the formation of cartilage (in relation to pressure), bone (in relation to shearing forces), and muscles (in relation to dilation forces). The cascade of molecules may be triggered by forces, which arise during physical cell and tissue interaction. Detailed morphological knowledge is mandatory to elucidate the exact location and timing of the regions where forces are exerted. Because this finding also holds true for the exact timing and location of signals, more 3D images of the developmental processes are required. Further research is also required to create methods for measuring forces within a tissue. The molecules whose presence and indispensability we are investigating appear to be mediators rather than creators of form. (c) 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16456854     DOI: 10.1002/dvdy.20704

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  7 in total

1.  Tooth-bone morphogenesis during postnatal stages of mouse first molar development.

Authors:  Vlasta Lungová; Ralf J Radlanski; Abigail S Tucker; Herbert Renz; Ivan Míšek; Eva Matalová
Journal:  J Anat       Date:  2011-03-22       Impact factor: 2.610

2.  Passive strain-induced matrix synthesis and organization in shape-specific, cartilaginous neotissues.

Authors:  Regina F MacBarb; Nikolaos K Paschos; Reedge Abeug; Eleftherios A Makris; Jerry C Hu; Kyriacos A Athanasiou
Journal:  Tissue Eng Part A       Date:  2014-12       Impact factor: 3.845

3.  Engineering functional anisotropy in fibrocartilage neotissues.

Authors:  Regina F MacBarb; Alison L Chen; Jerry C Hu; Kyriacos A Athanasiou
Journal:  Biomaterials       Date:  2013-09-24       Impact factor: 12.479

4.  Patterns of orofacial clefting in the facial morphology of bats: a possible naturally occurring model of cleft palate.

Authors:  David J A Orr; Emma C Teeling; Sébastien J Puechmaille; John A Finarelli
Journal:  J Anat       Date:  2016-06-27       Impact factor: 2.610

5.  Pressure from the lips and the tongue in children with class III malocclusion.

Authors:  Wen-hua Ruan; Ji-mei Su; Xiao-wei Ye
Journal:  J Zhejiang Univ Sci B       Date:  2007-05       Impact factor: 3.066

6.  The Use of Invisalign® System in the Management of the Orthodontic Treatment before and after Class III Surgical Approach.

Authors:  Renato Pagani; Fabrizio Signorino; Pier Paolo Poli; Pietro Manzini; Irene Panisi
Journal:  Case Rep Dent       Date:  2016-06-27

7.  The mechanical impact of col11a2 loss on joints; col11a2 mutant zebrafish show changes to joint development and function, which leads to early-onset osteoarthritis.

Authors:  Elizabeth A Lawrence; Erika Kague; Jessye A Aggleton; Robert L Harniman; Karen A Roddy; Chrissy L Hammond
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-09-24       Impact factor: 6.237

  7 in total

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