TY - JOUR
T1 - Common mechanisms in development and disease
T2 - BMP signaling in craniofacial development
AU - Graf, Daniel
AU - Malik, Zeba
AU - Hayano, Satoru
AU - Mishina, Yuji
N1 - Funding Information:
This review was written with support of funds from the School of Dentistry, University of Alberta (DG) , the Swiss National Science Foundation (grant 310030_135530 to DG), the National Institutes of Health ( R01DE020843 to YM), the Department of Defense ( W81XWH-11-2-0073 to YM), and the Japan Society for the Promotion of Science ( 15H06423 to SH).
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - BMP signaling is one of the key pathways regulating craniofacial development. It is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. It regulates development of its mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. Targeted mutations in the mouse have been instrumental to delineate the functional involvement of this signaling network in different aspects of craniofacial development. Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. The identification of intricate cellular interactions and underlying molecular pathways illustrate the importance of local fine-regulation of Bmp signaling to control proliferation, apoptosis, epithelial-mesenchymal interactions, and stem/progenitor differentiation during craniofacial development. Thus, BMP signaling contributes both to shape and functionality of our facial features. BMP signaling also regulates postnatal craniofacial growth and is associated with dental structures life-long. A more detailed understanding of BMP function in growth, homeostasis, and repair of postnatal craniofacial tissues will contribute to our ability to rationally manipulate this signaling network in the context of tissue engineering.
AB - BMP signaling is one of the key pathways regulating craniofacial development. It is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. It regulates development of its mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. Targeted mutations in the mouse have been instrumental to delineate the functional involvement of this signaling network in different aspects of craniofacial development. Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. The identification of intricate cellular interactions and underlying molecular pathways illustrate the importance of local fine-regulation of Bmp signaling to control proliferation, apoptosis, epithelial-mesenchymal interactions, and stem/progenitor differentiation during craniofacial development. Thus, BMP signaling contributes both to shape and functionality of our facial features. BMP signaling also regulates postnatal craniofacial growth and is associated with dental structures life-long. A more detailed understanding of BMP function in growth, homeostasis, and repair of postnatal craniofacial tissues will contribute to our ability to rationally manipulate this signaling network in the context of tissue engineering.
KW - BMP signaling
KW - Cleft palate
KW - Congenital malformations
KW - Craniofacial development
KW - Craniofacial malformations
KW - Gene targeting
KW - Tooth morphogenesis
UR - http://www.scopus.com/inward/record.url?scp=84957380732&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84957380732&partnerID=8YFLogxK
U2 - 10.1016/j.cytogfr.2015.11.004
DO - 10.1016/j.cytogfr.2015.11.004
M3 - Short survey
C2 - 26747371
AN - SCOPUS:84957380732
SN - 1359-6101
VL - 27
SP - 129
EP - 139
JO - Cytokine and Growth Factor Reviews
JF - Cytokine and Growth Factor Reviews
ER -