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Netrin induces down-regulation of its receptor Deleted in Colorectal Cancer through the ubiquitin–proteasome pathway in the embryonic cortical neuron

机译:Netrin通过胚胎皮质神经元中的泛素-蛋白酶体途径诱导其在大肠癌中缺失的受体的下调。

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摘要

The proper regulation of temporal and spatial expression of the axon guidance cues and their receptors is critical for the normal wiring of nervous system during development. Netrins, a family of secreted guidance cues, are involved in the midline crossing of spinal commissural axons and in the guidance of cortical efferents. Axons normally lose the responsiveness to their attractants when they arrive at their targets, where the attractant is produced. However the molecular mechanism is still unknown. We investigated the molecular mechanism of down-regulation of netrin-1 signaling in the embryonic cortical neurons. Netrin-1 induced the ubiquitination and proteolytic cleavage of Deleted in Colorectal Cancer (DCC), a trans-membrane receptor for netrin, in dissociated cortical neurons. A dramatic decrease of DCC level particularly on the cell surface was also observed after netrin-1 stimulation. Specific ubiquitin–proteasome inhibitors prevented the netrin-induced DCC cleavage and decrease of cell surface DCC. We suggest that the ligand-mediated down-regulation of DCC might participate in the loss of netrin-responsiveness in the developing nervous system.
机译:轴突引导线索及其受体的时空表达的适当调节对于发育过程中神经系统的正常布线至关重要。 Netrins是一个秘密的指导线索家族,参与脊椎连合轴突的中线交叉和皮层出射的指导。轴突通常在到达引诱剂产生的目标时失去对引诱剂的响应。然而,分子机制仍是未知的。我们调查了netrin-1信号在胚胎皮层神经元中下调的分子机制。 Netrin-1在分离的皮层神经元中诱导了大肠癌中的Deleted的泛素化和蛋白水解裂解,这是netrin的跨膜受体。在netrin-1刺激后,还观察到DCC水平显着下降,特别是在细胞表面。特定的泛素-蛋白酶体抑制剂可防止网蛋白诱导的DCC裂解并降低细胞表面DCC。我们建议DCC的配体介导的下调可能参与了神经系统发育中netrin反应性的丧失。

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