Literature DB >> 18391501

Tgf-beta regulation of suture morphogenesis and growth.

Joseph T Rawlins1, Lynne A Opperman.   

Abstract

Premature suture obliteration results in an inability of cranial and facial bones to grow, with resulting craniofacial dysmorphology requiring surgical correction. Understanding the biological signaling associated with suture morphogenesis will enable less invasive treatment of patients with fused sutures, combined with therapy using biological molecules. While a number of advances have been made in identifying the genetic etiologies of various craniosynostotic syndromes, the pathogenesis of this condition is still not completely understood. Recently, it has been shown that differential expression of various transforming growth factor-beta (Tgf-beta) isoforms plays a crucial role in regulating suture patency once the sutures have formed. It has also been shown that differential expression of Tgf-beta isoforms may also play a role in craniosynostosis by altering proliferation, differentiation, and apoptosis within the suture. This chapter focuses on the role of Tgf-beta in suture morphogenesis and growth, exploring Tgf-beta biology, receptors, signaling pathways, animal models, and expression in both normal and pathological sutures.

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Year:  2008        PMID: 18391501     DOI: 10.1159/000115038

Source DB:  PubMed          Journal:  Front Oral Biol        ISSN: 0301-536X


  10 in total

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5.  EphB3 as a potential mediator of developmental and reparative osteogenesis.

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6.  EphA4 as an effector of Twist1 in the guidance of osteogenic precursor cells during calvarial bone growth and in craniosynostosis.

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7.  Effects of Citalopram on Sutural and Calvarial Cell Processes.

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8.  Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis.

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9.  A review of hedgehog signaling in cranial bone development.

Authors:  Angel Pan; Le Chang; Alan Nguyen; Aaron W James
Journal:  Front Physiol       Date:  2013-04-02       Impact factor: 4.566

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  10 in total

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