The adaptor protein Nck-1 couples the netrin-1 receptor DCC (deleted in colorectal cancer) to the activation of the small GTPase Rac1 through an atypical mechanism

被引:89
作者
Li, XD
Meriane, M
Triki, I
Shekarabi, M
Kennedy, TE
Larose, L
Lamarche-Vane, N
机构
[1] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 2B2, Canada
[2] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Polypeptide Hormone Lab, Montreal, PQ H3A 2B2, Canada
关键词
D O I
10.1074/jbc.M205428200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Netrins are a family of secreted proteins that guide the migration of cells and axonal growth cones during development. DCC (deleted in colorectal cancer) is a receptor for netrin-1 implicated in mediating these responses. Here, we show that DCC interacts constitutively with the SH3/SH2 adaptor Nck in commissural neurons. This interaction is direct and requires the SH3 but not SH2 domains of Nck-1. Moreover, both DCC and Nck-1 associate with the actin cytoskeleton, and this association is mediated by DCC. A dominant negative Nck-1 inhibits the ability of DCC to induce neurite outgrowth in N1E-115 cells and to activate Rac1 in fibroblasts in response to netrin-1. These studies provide evidence for an important role of mammalian Nck-1 in a novel signaling pathway from an extracellular guidance cue to changes in the actin-based cytoskeleton responsible for axonal guidance.
引用
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页码:37788 / 37797
页数:10
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