Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling

被引:139
作者
Kléber, M
Lee, HY
Wurdak, H
Buchstaller, J
Riccomagno, MM
Ittner, LM
Suter, U
Epstein, DJ
Sommer, L [1 ]
机构
[1] ETH Honggerberg, Swiss Fed Inst Technol, Dept Biol, Inst Cell Biol, CH-8093 Zurich, Switzerland
[2] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Zurich, Univ Hosp Balgrist, Res Lab Calcium Metab, CH-8008 Zurich, Switzerland
关键词
D O I
10.1083/jcb.200411095
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Canonical Wnt signaling instructively promotes sensory neurogenesis in early neural crest stem cells (eNCSCs) (Lee, H. Y., M. Kleber, L. Hari, V. Brault, U. Suter, M. M. Taketo, R. Kemler, and L. Sommer. 2004. Science. 303: 1020-1023). However, during normal development Wnt signaling induces a sensory fate only in a subpopulation of eNCSCs while other cells maintain their stem cell features, despite the presence of Wnt activity. Hence, factors counteracting Wnt signaling must exist. Here, we show that bone morphogenic protein (BMP) signaling antagonizes the sensory fate-inducing activity of Wnt/beta-catenin. Intriguingly, Wnt and BMP act synergistically to suppress differentiation and to maintain NCSC marker expression and multipotency. Similar to NCSCs in vivo, NCSCs maintained in culture alter their responsiveness to instructive growth factors with time. Thus, stem cell development is regulated by combinatorial growth factor activities that interact with changing cell-intrinsic cues.
引用
收藏
页码:309 / 320
页数:12
相关论文
共 43 条
[1]   Interactions between Sox9 and β-catenin control chondrocyte differentiation [J].
Akiyama, H ;
Lyons, JP ;
Mori-Akiyama, Y ;
Yang, XH ;
Zhang, R ;
Zhang, ZP ;
Deng, JM ;
Taketo, MM ;
Nakamura, T ;
Behringer, RR ;
McCrea, PD ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2004, 18 (09) :1072-1087
[2]   A unified hypothesis on the lineage of neural stem cells [J].
Alvarez-Buylla, A ;
García-Verdugo, JM ;
Tramontin, AD .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (04) :287-293
[3]   Cell-intrinsic differences between stem cells from different regions of the peripheral nervous system regulate the generation of neural diversity [J].
Bixby, S ;
Kruger, GM ;
Mosher, JT ;
Joseph, NM ;
Morrison, SJ .
NEURON, 2002, 35 (04) :643-656
[4]   SOX9 is an intestine crypt transcription factor, is regulated by the Wnt pathway, and represses the CDX2 and MUC2 genes [J].
Blache, P ;
van de Wetering, M ;
Duluc, I ;
Domon, C ;
Berta, P ;
Freund, JN ;
Clevers, H ;
Jay, P .
JOURNAL OF CELL BIOLOGY, 2004, 166 (01) :37-47
[5]   Canonical Wnt activity regulates trunk neural crest delamination linking BMP/noggin signaling with G1/S transition [J].
Burstyn-Cohen, T ;
Stanleigh, J ;
Sela-Donenfeld, D ;
Kalcheim, C .
DEVELOPMENT, 2004, 131 (21) :5327-5339
[6]  
DasGupta R, 1999, DEVELOPMENT, V126, P4557
[7]   Control of neural crest cell fate by the Wnt signalling pathway [J].
Dorsky, RI ;
Moon, RT ;
Raible, DW .
NATURE, 1998, 396 (6709) :370-373
[8]   BRN-3.0 EXPRESSION IDENTIFIES EARLY POSTMITOTIC CNS NEURONS AND SENSORY NEURAL PRECURSORS [J].
FEDTSOVA, NG ;
TURNER, EE .
MECHANISMS OF DEVELOPMENT, 1995, 53 (03) :291-304
[9]  
FRASER SE, 1991, DEVELOPMENT, V112, P913
[10]   Ectodermal Wnt function as a neural crest inducer [J].
Garcia-Castro, MI ;
Marcelle, C ;
Bronner-Fraser, M .
SCIENCE, 2002, 297 (5582) :848-851