Molecular mechanisms of neural crest formation

被引:173
作者
LaBonne, C [1 ]
Bronner-Fraser, M [1 ]
机构
[1] CALTECH, Div Biol 139 74, Pasadena, CA 91125 USA
关键词
BMP; Wnt; FGF; chick; Xenopus;
D O I
10.1146/annurev.cellbio.15.1.81
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The neural crest is a transient population of multipotent precursor cells named for its site of origin at the crest of the closing neural folds in vertebrate embryos. Following neural tube closure, these cells become migratory and populate diverse regions throughout the embryo where they give rise to most of the neurons and support cells of the peripheral nervous system (PNS), pigment cells, smooth muscle, craniofacial cartilage, and bone. Because of its remarkable ability to generate such diverse derivatives, the neural crest has fascinated developmental biologists for over one hundred years. A great deal has been learned about the migratory pathways neural crest cells follow and the signals that may trigger their differentiation, but until recently comparatively little was known about earlier steps in neural crest development. In the past few years progress has been made in understanding these earlier events, including how the precursors of these multipotent cells are specified in the early embryo and the mechanisms by which they become migratory. In this review, we first examine the mechanisms underlying neural crest induction, paying particular attention to a number of growth factor and transcription factor families that have been implicated in this process. We also discuss when and how the fate of neural crest precursors may diverge from those of nearby neural and epidermal populations. Finally, we review recent advances in our understanding of how neural crest cells become migratory and address the process of neural crest diversification.
引用
收藏
页码:81 / 112
页数:32
相关论文
共 182 条
[1]   Neural induction in whole chick embryo cultures by FGF [J].
Alvarez, IS ;
Araujo, M ;
Nieto, MA .
DEVELOPMENTAL BIOLOGY, 1998, 199 (01) :42-54
[2]  
ARUGA J, 1994, J NEUROCHEM, V63, P1880
[3]   Identification and characterization of Zic4, a new member of the mouse Zic gene family [J].
Aruga, J ;
Yozu, A ;
Hayashizaki, Y ;
Okazaki, Y ;
Chapman, VM ;
Mikoshiba, K .
GENE, 1996, 172 (02) :291-294
[4]   The mouse Zic gene family - Homologues of the Drosophila pair-rule gene odd-paired [J].
Aruga, J ;
Nagai, T ;
Tokuyama, T ;
Hayashizaki, Y ;
Okazaki, Y ;
Chapman, VM ;
Mikoshiba, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (02) :1043-1047
[5]   ANALYSIS OF THE DEVELOPMENTAL EFFECTS OF A LETHAL MUTATION IN THE HOUSE MOUSE [J].
AUERBACH, R .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1954, 127 (02) :305-+
[6]   The origins of the neural crest. Part I: Embryonic induction [J].
Baker, CVH ;
Bronner-Fraser, M .
MECHANISMS OF DEVELOPMENT, 1997, 69 (1-2) :3-11
[7]   The origins of the neural crest. Part II: an evolutionary perspective [J].
Baker, CVH ;
Bronner-Fraser, M .
MECHANISMS OF DEVELOPMENT, 1997, 69 (1-2) :13-29
[8]  
Baker CVH, 1997, DEVELOPMENT, V124, P3077
[9]  
Bang AG, 1997, DEVELOPMENT, V124, P2075
[10]  
Bei M, 1998, DEVELOPMENT, V125, P4325