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首页> 外文期刊>Neuron >Interplay of cell-autonomous and nonautonomous mechanisms tailors synaptic connectivity of converging axons in vivo
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Interplay of cell-autonomous and nonautonomous mechanisms tailors synaptic connectivity of converging axons in vivo

机译:细胞自主和非自主机制的相互作用可调节体内融合轴突的突触连通性。

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摘要

Neurons receive input from diverse afferents but form stereotypic connections with each axon type to execute their precise functions. Developmental mechanisms that specify the connectivity of individual axons across populations of converging afferents are not well-understood. Here, we untangled the contributions of activity-dependent and independent interactions that regulate the connectivity of afferents providing major and minor input onto a neuron. Individual transmission-deficient retinal bipolar cells (BCs) reduced synapses with retinal ganglion cells (RGCs), but active BCs of the same type sharing the dendrite surprisingly did not compensate for this loss. Genetic ablation of some BC neighbors resulted in increased synaptogenesis by the remaining axons in a transmission-independent manner. Presence, but not transmission, of the major BC input also dissuades wiring with the minor input and with synaptically compatible but functionally mismatched afferents. Cell-autonomous, activity-dependent and nonautonomous, activity-independent mechanisms thus together tailor connectivity of individual axons among converging inner retinal afferents.
机译:神经元接收来自不同传入的输入,但与每种轴突类型形成定型联系以执行其精确功能。不能很好地理解在汇聚传入人口中指定各个轴突之间连通性的发展机制。在这里,我们理清了活动依赖和独立相互作用的贡献,这些相互作用调节了在神经元上提供主要和次要输入的传入连接的连通性。个别传播缺陷的视网膜双极细胞(BCs)减少了与视网膜神经节细胞(RGCs)的突触,但共享树突的相同类型的活动BCs令人惊讶地不能弥补这种损失。某些BC邻居的遗传消融导致其余轴突以不依赖传播的方式增加突触形成。主要BC输入的存在(而不是传输)也阻止了次要输入以及与突触兼容但在功能上不匹配的传入传入的布线。因此,细胞自主的,与活动有关的和非自主的,与活动无关的机制共同调整了会聚的内部视网膜传入神经之间各个轴突的连通性。

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