Cranial Neural Crest Cells on the Move: Their Roles in Craniofacial Development

被引:195
|
作者
Cordero, Dwight R. [1 ,2 ]
Brugmann, Samantha [3 ]
Chu, Yvonne [1 ,2 ]
Bajpai, Ruchi [4 ]
Jame, Maryam [3 ]
Helms, Jill A. [3 ]
机构
[1] Brigham & Womens Hosp, Dept Obstet Gynecol & Reprod Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Stanford Univ, Sch Med, Dept Surg, Div Plast & Reconstruct Surg, Palo Alto, CA 94304 USA
[4] Stanford Univ, Sch Med, Dept Dev Biol, Palo Alto, CA 94304 USA
关键词
neural crest cells; craniofacial development; neurocristopathies; MOWAT-WILSON-SYNDROME; EPITHELIAL-MESENCHYMAL TRANSITIONS; NONSYNDROMIC CLEFT-LIP; CHARGE-SYNDROME; E-CADHERIN; HIRSCHSPRUNG-DISEASE; FOREGUT ENDODERM; VERTEBRATE HEAD; WAARDENBURG-SYNDROME; PHENOTYPIC SPECTRUM;
D O I
10.1002/ajmg.a.33702
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The craniofacial region is assembled through the active migration of cells and the rearrangement and sculpting of facial prominences and pharyngeal arches, which consequently make it particularly susceptible to a large number of birth defects. Genetic, molecular, and cellular processes must be temporally and spatially regulated to culminate in the three-dimension structures of the face. The starting constituent for the majority of skeletal and connective tissues in the face is a pluripotent population of cells, the cranial neural crest cells (NCCs). In this review we discuss the newest scientific findings in the development of the craniofacial complex as related to NCCs. Furthermore, we present recent findings on NCC diseases called neurocristopathies and, in doing so, provide clinicians with new tools for understanding a growing number of craniofacial genetic disorders. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:270 / 279
页数:10
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