Wnt signaling and stem cell control

被引:448
作者
Nusse, Roel [1 ]
机构
[1] Stanford Univ, Dept Dev Biol, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
Wnt; stem cells; self-renewal; signal transduction; niche;
D O I
10.1038/cr.2008.47
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Wnt signaling has been implicated in the control over various types of stem cells and may act as a niche factor to maintain stem cells in a self-renewing state. As currently understood, Wnt proteins bind to receptors of the Frizzled and LRP families on the cell surface. Through several cytoplasmic relay components, the signal is transduced to B-catenin, which then enters the nucleus and forms a complex with TCF to activate transcription of Wnt target genes. Wnts can also signal through tyrosine kinase receptors, in particular the ROR and RYK receptors, leading to alternative modes of Wnt signaling. During the growth of tissues, these ligands and receptors are dynamically expressed, often transcriptionally controlled by Wnt signals themselves, to ensure the right balance between proliferation and differentiation. Isolated Wnt proteins are active on a variety of stem cells, including neural, mammary and embryonic stem cells. In general, Wnt proteins act to maintain the undifferentiated state of stem cells, while other growth factors instruct the cells to proliferate. These other factors include FGF and EGF, signaling through tyrosine kinase pathways.
引用
收藏
页码:523 / 527
页数:5
相关论文
共 48 条
[1]   Wntless, a conserved membrane protein dedicated to the secretion of Wnt proteins from signaling cells [J].
Bänziger, Carla ;
Soldini, Davide ;
Schuett, Corina ;
Zipperlen, Peder ;
Hausmann, George ;
Basler, Konrad .
CELL, 2006, 125 (03) :509-522
[2]   Secretion of Wnt Ligands requires Evi, a conserved transmembrane protein [J].
Bartscherer, Kerstin ;
Pelte, Nadege ;
Ingelfinger, Dierk ;
Boutros, Michael .
CELL, 2006, 125 (03) :523-533
[3]   A new member of the frizzled family from Drosophila functions as a Wingless receptor [J].
Bhanot, P ;
Brink, M ;
Samos, CH ;
Hsieh, JC ;
Wang, YS ;
Macke, JP ;
Andrew, D ;
Nathans, J ;
Nusse, R .
NATURE, 1996, 382 (6588) :225-230
[4]   Linking colorectal cancer to Wnt signaling [J].
Bienz, M ;
Clevers, H .
CELL, 2000, 103 (02) :311-320
[5]   β-arrestin 2 mediates endocytosis of type III TGF-β receptor and down-regulation of its signaling [J].
Chen, W ;
Kirkbride, KC ;
How, T ;
Nelson, CD ;
Mo, JY ;
Frederick, JP ;
Wang, XF ;
Lefkowitz, RJ ;
Blobe, GC .
SCIENCE, 2003, 301 (5638) :1394-1397
[6]   Regulation of cerebral cortical size by control of cell cycle exit in neural precursors [J].
Chenn, A ;
Walsh, CA .
SCIENCE, 2002, 297 (5580) :365-369
[7]   A dedicated Wnt secretion factor [J].
Ching, Wendy ;
Nusse, Roel .
CELL, 2006, 125 (03) :432-433
[8]   Wnt gradient formation requires retromer function in Wnt-producing cells [J].
Coudreuse, DYM ;
Roël, G ;
Betist, MC ;
Destrée, O ;
Korswagen, HC .
SCIENCE, 2006, 312 (5775) :921-924
[9]   Casein kinase 1γ couples Wnt receptor activation to cytoplasmic signal transduction [J].
Davidson, G ;
Wu, W ;
Shen, JL ;
Bilic, J ;
Fenger, U ;
Stannek, P ;
Glinka, A ;
Niehrs, C .
NATURE, 2005, 438 (7069) :867-872
[10]   The Ror receptor tyrosine kinase family [J].
Forrester, WC .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (01) :83-96