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Synaptic uSIRPation: The active neuron reigns over presynaptic partners

机译:突触的uSIRP化:活跃的神经元统​​治突触前的伙伴。

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What mechanisms control the synaptic wiring of neurons? Although trans-synaptic adhesion complexes can induce and specify synapse formation1 and glia-secreted factors modulate the extent to which neurons can assemble synapses2, the molecular mechanisms through which neuronal activity guides synaptogenesis remain unclear. Conceptually, activity should be a key element in this process, as it could give active neurons a competitive edge over the inactive ones and thereby promote the integration of active neurons into networks. A study by Toth et a} published in this issue of Nature Neuroscience finds that active neurons shed a soluble fragment of the signal regulatory protein (SIRP)-oc to generate a synaptogenic signal, allowing them to govern presynaptic neurons and induce new synapses (Fig. 1).
机译:哪些机制控制神经元的突触连线?尽管跨突触粘附复合物可以诱导并确定突触的形成1和神经胶质分泌因子调节神经元组装突触的程度2,但神经元活性指导突触形成的分子机制仍不清楚。从概念上讲,活动应该是此过程中的关键要素,因为它可以使活动神经元比不活动神经元具有竞争优势,从而促进活动神经元整合到网络中。 Toth等人在本期《自然神经科学》上发表的一项研究发现,活跃的神经元释放了信号调节蛋白(SIRP)-oc的可溶性片段以产生突触信号,从而使它们能够控制突触前神经元并诱导新的突触(图。1)。

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