Literature DB >> 15305282

Conserved molecular program regulating cranial and appendicular skeletogenesis.

B Frank Eames, Jill A Helms.   

Abstract

The majority of in vivo studies on bone and cartilage differentiation are carried out using the appendicular skeleton as a model system, with the implicit assumption that skeletal formation is equivalent throughout the body. This assumption persists, despite differences in the cellular origins of the skeletogenic precursors. To test the hypothesis that a fundamental set of genes directs skeletal cell differentiation throughout the body, we analyzed cartilage and bone of the chick limb and head during mesenchymal condensation, and when the skeletal tissues had matured. First, we analyzed the expression patterns of transcription factors in early skeletogenic condensations, which revealed similarities among skeletal cell specification in the limb and head. For example, skeletogenic condensations that undergo endochondral ossification had equivalent expression patterns of skeletogenic transcription factors in both limb and head. In the head, many elements also differentiate through intramembranous ossification, or through persistent cartilage formation. Our analyses of these skeletogenic condensations revealed that a unique expression pattern of transcription factors distinguishes among three skeletal tissue fates. The vasculature was excluded from all three skeletogenic condensations, demonstrating that this is not a characteristic unique to endochondral ossification. Second, we compared three different types of more mature cartilage and bone tissue in both the limb and the head, by analyzing a variety of skeletal collagens and signaling molecules. Histological and molecular markers of cartilage and bone generally were conserved between the limb and head skeletons, although we uncovered subtle differences in signaling pathways that might influence cranial and appendicular skeletogenesis.

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Year:  2004        PMID: 15305282     DOI: 10.1002/dvdy.20134

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


  29 in total

1.  Developmental expression of Dkk1-3 and Mmp9 and apoptosis in cranial base of mice.

Authors:  Xuguang Nie; Keijo Luukko; Karianne Fjeld; Inger Hals Kvinnsland; Päivi Kettunen
Journal:  J Mol Histol       Date:  2006-03-07       Impact factor: 2.611

2.  Concerted action of Msx1 and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development.

Authors:  Jun Han; Mamoru Ishii; Pablo Bringas; Richard L Maas; Robert E Maxson; Yang Chai
Journal:  Mech Dev       Date:  2007-07-10       Impact factor: 1.882

Review 3.  Wnt signaling and skeletal development.

Authors:  Fei Liu; Sean Kohlmeier; Cun-Yu Wang
Journal:  Cell Signal       Date:  2007-11-28       Impact factor: 4.315

4.  Mesenchymal stem cells systemically injected into femoral marrow of dogs home to mandibular defects to enhance new bone formation.

Authors:  Xian Liu; Xuejuan Liao; En Luo; Wenchuan Chen; Chongyun Bao; Hockin H K Xu
Journal:  Tissue Eng Part A       Date:  2014-01-20       Impact factor: 3.845

5.  Two developmental modules establish 3D beak-shape variation in Darwin's finches.

Authors:  Ricardo Mallarino; Peter R Grant; B Rosemary Grant; Anthony Herrel; Winston P Kuo; Arhat Abzhanov
Journal:  Proc Natl Acad Sci U S A       Date:  2011-02-22       Impact factor: 11.205

6.  Occipital foramina development involves localised regulation of mesenchyme proliferation and is independent of apoptosis.

Authors:  Sophia E Akbareian; Andrew A Pitsillides; Raymond G Macharia; Imelda M McGonnell
Journal:  J Anat       Date:  2015-06       Impact factor: 2.610

7.  Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesis.

Authors:  Sarah J Gignac; Sara Hosseini-Farahabadi; Takashi Akazawa; Nathan J Schuck; Katherine Fu; Joy M Richman
Journal:  Hum Mol Genet       Date:  2019-07-15       Impact factor: 6.150

8.  Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins.

Authors:  Amy L Donner; Trevor Williams
Journal:  Dev Dyn       Date:  2006-05       Impact factor: 3.780

9.  Mesenchyme-dependent BMP signaling directs the timing of mandibular osteogenesis.

Authors:  Amy E Merrill; B Frank Eames; Scott J Weston; Thayer Heath; Richard A Schneider
Journal:  Development       Date:  2008-02-20       Impact factor: 6.868

10.  Skeletogenesis in the swell shark Cephaloscyllium ventriosum.

Authors:  B Frank Eames; Nancy Allen; Jonathan Young; Angelo Kaplan; Jill A Helms; Richard A Schneider
Journal:  J Anat       Date:  2007-05       Impact factor: 2.610

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