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Astrocyte response to motor neuron injury promotes structural synaptic plasticity via STAT3-regulated TSP-1 expression

机译:星形胶质细胞对运动神经元损伤的反应通过STAT3调节的TSP-1表达促进结构突触可塑性

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The role of remote astrocyte (AC) reaction to central or peripheral axonal insult is not clearly understood. Here we use a transgenic approach to compare the direct influence of normal with diminished AC reactivity on neuronal integrity and synapse recovery following extracranial facial nerve transection in mice. Our model allows straightforward interpretations of AC–neuron signalling by reducing confounding effects imposed by inflammatory cells. We show direct evidence that perineuronal reactive ACs play a major role in maintaining neuronal circuitry following distant axotomy. We reveal a novel function of astrocytic signal transducer and activator of transcription-3 ( STAT3 ). STAT3 regulates perineuronal astrocytic process formation and re-expression of a synaptogenic molecule, thrombospondin-1 ( TSP-1 ), apart from supporting neuronal integrity. We demonstrate that, through this new pathway, TSP-1 is responsible for the remote AC-mediated recovery of excitatory synapses onto axotomized motor neurons in adult mice. These data provide new targets for neuroprotective therapies via optimizing AC-driven plasticity.
机译:尚不清楚远端星形胶质细胞(AC)反应对中枢或外周轴突损伤的作用。在这里,我们使用转基因方法比较正常和交流反应性降低对小鼠颅外面神经横断后神经元完整性和突触恢复的直接影响。我们的模型通过减少炎症细胞施加的混杂效应,可以直接解释AC-神经元信号。我们显示直接证据表明,神经周围神经反应性AC在遥远的轴切术后维持神经元回路中起主要作用。我们揭示了星形细胞信号转导和转录激活因子3(STAT3)的新型功能。 STAT3除了支持神经元完整性外,还调节神经元星形细胞过程的形成和突触形成分子thrombospondin-1(TSP-1)的重新表达。我们证明,通过这一新途径,TSP-1负责成年小鼠中远程AC介导的兴奋性突触到轴突化运动神经元上的远程恢复。这些数据通过优化AC驱动的可塑性为神经保护疗法提供了新的目标。

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