Wnt Signaling Gradients Establish Planar Cell Polarity by Inducing Vangl2 Phosphorylation through Ror2

被引:426
作者
Gao, Bo [1 ]
Song, Hai [1 ]
Bishop, Kevin [1 ]
Elliot, Gene [1 ]
Garrett, Lisa [1 ]
English, Milton A. [1 ]
Andre, Philipp [1 ]
Robinson, James [1 ]
Sood, Raman [1 ]
Minami, Yasuhiro [2 ]
Economides, Aris N. [3 ]
Yang, Yingzi [1 ]
机构
[1] NHGRI, Bethesda, MD 20892 USA
[2] Kobe Univ, Fac Med Sci, Dept Physiol & Cell Biol, Chuo Ku, Kobe, Hyogo 6500017, Japan
[3] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
关键词
RECEPTOR TYROSINE KINASE; NEURAL-TUBE DEFECTS; RECESSIVE ROBINOW-SYNDROME; BRACHYDACTYLY TYPE-B; I-EPSILON; LOOP-TAIL; DROSOPHILA; PATHWAY; MUTATIONS; CATENIN;
D O I
10.1016/j.devcel.2011.01.001
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
It is fundamentally important that signaling gradients provide positional information to govern morphogenesis of multicellular organisms. Morphogen gradients can generate different cell types in specific spatial order at distinct threshold concentrations. However, it is largely unknown whether and how signaling gradients also control cell polarities by acting as global cues. Here, we show that Wnt signaling gradient provides directional information to a field of cells. Vangl2, a core component in planar cell polarity, forms Wnt-induced receptor complex with Ror2 to sense Wnt dosages. Wnts dose-dependently induce Vangl2 phosphorylation of serine/threonine residues and Vangl2 activities depend on its levels of phosphorylation. In the limb bud, Wnt5a signaling gradient controls limb elongation by establishing PCP in chondrocytes along the proximal-distal axis through regulating Vangl2 phosphorylation. Our studies have provided new insight to Robinow syndrome, Brachydactyly Type B1, and spinal bifida which are caused by mutations in human ROR2, WNT5A, or VANGL.
引用
收藏
页码:163 / 176
页数:14
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