Wnt Won the War: Antagonistic Role of Wnt over Shh Controls Dorso-Ventral Patterning of the Vertebrate Neural Tube

被引:114
作者
Ulloa, Fausto [2 ,3 ,4 ]
Marti, Elisa [1 ]
机构
[1] CSIC, Inst Biol Mol Barcelona, E-08028 Barcelona, Spain
[2] Univ Barcelona, Dept Cell Biol, Barcelona, Spain
[3] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Barcelona, Spain
[4] Inst Res Biomed, Dev Neurobiol & Regenerat Unit, Barcelona, Spain
关键词
Wnt; beta-catenin; Sonic hedgehog; Gli; neural tube; spinal cord; patterning; DORSAL SPINAL-CORD; CENTRAL-NERVOUS-SYSTEM; SONIC-HEDGEHOG; BETA-CATENIN; GLI PROTEINS; POSITIONAL INFORMATION; NEURONAL SPECIFICATION; FATE SPECIFICATION; CELL-TYPES; TGF-BETA;
D O I
10.1002/dvdy.22058
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The spinal cord has been used as a model to dissect the mechanisms that govern the patterning of tissues during animal development, since the principles that rule the dorso-ventral patterning of the neural tube are applicable to other systems. Signals that determine the dorso-ventral axis of the spinal cord include Sonic hedgehog (Shh), acting as a bona fide morphogenetic signal to determine ventral progenitor identities, and members of the Bmp and the Wnt families, acting in the dorsal neural tube. Although Wnts have been initially recognized as important in proliferation of neural progenitor cells, their role in the dorso-ventral patterning has been controversial. In this review, we discuss recent reports that show an important contribution of the Wnt canonical pathway in dorso-ventral pattern formation. These data allow building a model by which the ventralizing activity of Shh is antagonized by Wnt activity through the expression of Gli3, a potent inhibitor of the Shh pathway. Therefore, antagonistic interactions between canonical Wnt, promoting dorsal identities, and Shh pathways, inducing ventral ones, would define the dorso-ventral patterning of the developing central nervous system. Developmental Dynamics 239:69-76, 2010. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:69 / 76
页数:8
相关论文
共 78 条
[1]   Human GLI3 Intragenic Conserved Non-Coding Sequences Are Tissue-Specific Enhancers [J].
Abbasi, Amir Ali ;
Paparidis, Zissis ;
Malik, Sajid ;
Goode, Debbie K. ;
Callaway, Heather ;
Elgar, Greg ;
Grzeschik, Karl-Heinz .
PLOS ONE, 2007, 2 (04)
[2]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[3]   The Drosophila smoothened gene encodes a seven-pass membrane protein, a putative receptor for the hedgehog signal [J].
Alcedo, J ;
Ayzenzon, M ;
VonOhlen, T ;
Noll, M ;
Hooper, JE .
CELL, 1996, 86 (02) :221-232
[4]   The emergent design of the neural tube:: prepattern, SHH morphogan and GLI code [J].
Altaba, AR ;
Nguyên, V ;
Palma, V .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (05) :513-521
[5]  
Altaba ARI, 1999, DEVELOPMENT, V126, P3205
[6]  
Altaba ARI, 1998, DEVELOPMENT, V125, P2203
[7]   Wnt canonical pathway restricts graded Shh/Gli patterning activity through the regulation of Gli3 expression [J].
Alvarez-Medina, Roberto ;
Cayuso, Jordi ;
Okubo, Tadashi ;
Takada, Shinji ;
Marti, Elisa .
DEVELOPMENT, 2008, 135 (02) :237-247
[8]  
Aza-Blanc P, 2000, DEVELOPMENT, V127, P4293
[9]   Effects of canonical Wnt signaling on dorso-ventral specification of the mouse telencephalon [J].
Backman, M ;
Machon, O ;
Mygland, L ;
van den Bout, CJ ;
Zhong, WM ;
Taketo, MM ;
Krauss, S .
DEVELOPMENTAL BIOLOGY, 2005, 279 (01) :155-168
[10]   All mouse ventral spinal cord patterning by hedgehog is Gli dependent and involves an activator function of Gli3 [J].
Bai, CB ;
Stephen, D ;
Joyner, AL .
DEVELOPMENTAL CELL, 2004, 6 (01) :103-115