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Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number.

机译:依赖于活性的MEF2转录因子调节抑制兴奋性突触数目。

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In the mammalian nervous system, neuronal activity regulates the strength and number of synapses formed. The genetic program that coordinates this process is poorly understood. We show that myocyte enhancer factor 2 (MEF2) transcription factors suppressed excitatory synapse number in a neuronal activity- and calcineurin-dependent manner as hippocampal neurons formed synapses. In response to increased neuronal activity, calcium influx into neurons induced the activation of the calcium/calmodulin-regulated phosphatase calcineurin, which dephosphorylated and activated MEF2. When activated, MEF2 promoted the transcription of a set of genes, including arc and synGAP, that restrict synapse number. These findings define an activity-dependent transcriptional program that may control synapse number during development.
机译:在哺乳动物的神经系统中,神经元活动调节形成的突触的强度和数量。协调这一过程的遗传程序知之甚少。我们显示,心肌细胞增强因子2(MEF2)转录因子抑制海马神经元形成突触的神经元活动和钙调神经磷酸酶依赖性的兴奋性突触数量。响应于增加的神经元活性,钙流入神经元诱导了钙/钙调蛋白调节的磷酸酶钙调神经磷酸酶的活化,其使磷酸化并激活了MEF2。激活后,MEF2促进限制突触数量的一组基因的转录,包括arc和synGAP。这些发现定义了一个活动依赖的转录程序,可以在发育过程中控制突触的数量。

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