Jeong Myong-Ho, Ho Seok-Man, Vuong Tuan Anh, Jo Shin-Bum, Liu Guizhong, Aaronson Stuart A, Leem Young-Eun, Kang Jong-Sun
Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Samsung Biomedical Research Institute, Suwon 440-746, Republic of Korea.
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Nat Commun. 2014 Nov 19;5:5455. doi: 10.1038/ncomms6455.
Canonical Wnt signalling regulates expansion of neural progenitors and functions as a dorsalizing signal in the developing forebrain. In contrast, the multifunctional co-receptor Cdo promotes neuronal differentiation and is important for the function of the ventralizing signal, Shh. Here we show that Cdo negatively regulates Wnt signalling during neurogenesis. Wnt signalling is enhanced in Cdo-deficient cells, leading to impaired neuronal differentiation. The ectodomains of Cdo and Lrp6 interact via the Ig2 repeat of Cdo and the LDLR repeats of Lrp6, and the Cdo Ig2 repeat is necessary for Cdo-dependent Wnt inhibition. Furthermore, the Cdo-deficient dorsal forebrain displays stronger Wnt signalling activity, increased cell proliferation and enhanced expression of the dorsal markers and Wnt targets, Pax6, Gli3, Axin2. Therefore, in addition to promoting ventral central nervous system cell fates with Shh, Cdo promotes neuronal differentiation by suppression of Wnt signalling and provides a direct link between two major dorsoventral morphogenetic signalling pathways.
经典Wnt信号通路调控神经祖细胞的增殖,并在发育中的前脑作为背侧化信号发挥作用。相比之下,多功能共受体Cdo促进神经元分化,并且对腹侧化信号Shh的功能很重要。在此我们表明,Cdo在神经发生过程中对Wnt信号通路起负调控作用。在缺乏Cdo的细胞中Wnt信号通路增强,导致神经元分化受损。Cdo和Lrp6的胞外结构域通过Cdo的Ig2重复序列和Lrp6的LDLR重复序列相互作用,并且Cdo的Ig2重复序列对于Cdo依赖的Wnt抑制是必需的。此外,缺乏Cdo的背侧前脑表现出更强的Wnt信号活性、增加的细胞增殖以及背侧标志物和Wnt靶标Pax6、Gli3、Axin2的表达增强。因此,除了与Shh一起促进腹侧中枢神经系统细胞命运外,Cdo还通过抑制Wnt信号通路促进神经元分化,并在两条主要的背腹形态发生信号通路之间提供了直接联系。