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首页> 外文期刊>Neuron >SAD Kinases Sculpt Axonal Arbors of Sensory Neurons through Long- and Short-Term Responses to Neurotrophin Signals
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SAD Kinases Sculpt Axonal Arbors of Sensory Neurons through Long- and Short-Term Responses to Neurotrophin Signals

机译:SAD激酶通过对神经营养蛋白信号的长期和短期响应来雕刻感觉神经元的轴突。

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摘要

Extrinsic cues activate intrinsic signaling mechanisms to pattern neuronal shape and connectivity. We showed previously that three cytoplasmic Ser/Thr kinases, LKB1, SAD-A, and SAD-B, control early axon-dendrite polarization in forebrain neurons. Here, we assess their role in other neuronal types. We found that all three kinases are dispensable for axon formation outside of the cortex but that SAD kinases are required for formation of central axonal arbors by subsets of sensory neurons. The requirement for SAD kinases is most prominent in NT-3 dependent neurons. SAD kinases transduce NT-3 signals in two ways through distinct pathways. First, sustained NT-3/TrkC signaling increases SAD protein levels. Second, short-duration NT-3/TrkC signals transiently activate SADs by inducing dephosphorylation of C-terminal domains, thereby allowing activating phosphorylation of the kinase domain. We propose that SAD kinases integrate long- and short-duration signals from extrinsic cues to sculpt axon arbors within the CNS.
机译:外在线索激活内在的信号传导机制以图案化神经元的形状和连通性。我们以前表明,三种细胞质Ser / Thr激酶LKB1,SAD-A和SAD-B控制着前脑神经元的早期轴突-树突极化。在这里,我们评估了它们在其他神经元类型中的作用。我们发现,这三种激酶对于皮层以外的轴突形成都是必不可少的,但SAD激酶是感觉神经元子集形成中枢轴突柄所必需的。 SAD激酶的需求在NT-3依赖性神经元中最为突出。 SAD激酶通过不同的途径以两种方式转导NT-3信号。首先,持续的NT-3 / TrkC信号传导会增加SAD蛋白水平。其次,短时NT-3 / TrkC信号通过诱导C末端结构域的去磷酸化来瞬时激活SAD,从而激活激酶结构域的磷酸化。我们建议,SAD激酶整合了来自外部线索的长时和短时信号,以雕刻CNS内的轴突柄。

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