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Design Logic of a Cannabinoid Receptor Signaling Network That Triggers Neurite Outgrowth

机译:触发神经突生长的大麻素受体信号网络的设计逻辑

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摘要

Cannabinoid receptor 1 (CB1R) regulates neuronal differentiation. To understand the logic underlying decision-making in the signaling network controlling CB1R-induced neurite outgrowth, we profiled the activation of several hundred transcription factors after cell stimulation. We assembled an in silico signaling network by connecting CB1R to 23 activated transcription factors. Statistical analyses of this network predicted a role for the breast cancer 1 protein BRCA1 in neuronal differentiation and a new pathway from CB1R through phosphoinositol 3-kinase to the transcription factor paired box 6 (PAX6). Both predictions were experimentally confirmed. Results of transcription factor activation experiments that used pharmacological inhibitors of kinases revealed a network organization of partial OR gates regulating kinases stacked above AND gates that control transcription factors, which together allow for distributed decision-making in CB1R-induced neurite outgrowth.
机译:大麻素受体1(CB1R)调节神经元分化。为了了解控制CB1R诱导的神经突生长的信号网络中决策的逻辑基础,我们分析了细胞刺激后数百种转录因子的激活。通过将CB1R连接到23个激活的转录因子,我们组装了一个计算机信号网络。该网络的统计分析预测了乳腺癌1蛋白BRCA1在神经元分化中的作用以及从CB1R通过磷酸肌醇3激酶到转录因子配对盒6(PAX6)的新途径。两项预测均通过实验证实。使用激酶的药理学抑制剂的转录因子激活实验的结果表明,调节连接于控制转录因子的AND门上方的激酶的部分OR门的网络组织,这些门共同构成了CB1R诱导的神经突增生的分布式决策。

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