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Alteration of Nrp1 signaling at different stages of olfactory neuron maturation promotes glomerular shifts along distinct axes in the olfactory bulb

机译:Nrp1信号在嗅觉神经元成熟的不同阶段的改变促进了嗅球沿着嗅球中不同轴的移动

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Building the topographic map in the mammalian olfactory bulb is explained by a model based on two axes along which sensory neurons are guided: one dorsoventral and one anteroposterior. This latter axis relies on specific expression levels of Nrp1. To evaluate the role of this receptor in this process, we used an in vivo genetic approach to decrease or suppress Nrp1 in specific neuronal populations and at different time points during axonal targeting. We observed, in neurons that express the M71 or M72 odorant receptors, that Nrp1 inactivation leads to two distinct wiring alterations, depending on the time at which Nrp1 expression is altered: first, a surprising dorsal shift of the M71 and M72 glomeruli, which often fuse with their contralateral counterparts, and second the formation of anteriorized glomeruli. The two phenotypes are partly recapitulated in mice lacking the Nrp1 ligand Sema3A and in mice whose sensory neurons express an Nrp1 mutant unable to bind Sema3A. Using a mosaic conditional approach, we show that M71 axonal fibers can bypass the Nrp1 signals that define their target area, since they are hijacked and coalesce with Nrp1-deficient M71-expressing axons that target elsewhere. Together, these findings show drastically different axonal targeting outcomes dependent on the timing at which Nrp1/Sema3A signaling is altered.
机译:建立在哺乳动物嗅球中的地形图是由一个基于两个轴的模型来解释的,沿着该轴可引导感觉神经元:一个背腹和一个前后位。后一个轴依赖于Nrp1的特定表达水平。为了评估该受体在此过程中的作用,我们使用了一种体内遗传方法来减少或抑制特定神经元群体中以及轴突靶向过程中不同时间点的Nrp1。我们观察到在表达M71或M72气味受体的神经元中,Nrp1失活导致两个明显的接线改变,具体取决于Nrp1表达改变的时间:首先,M71和M72肾小球的令人惊讶的背侧移位,这通常是与对侧的对等融合,其次形成前肾小球。在缺少Nrp1配体Sema3A的小鼠和其感觉神经元表达无法结合Sema3A的Nrp1突变体的小鼠中,这两种表型被部分概括。使用镶嵌条件方法,我们显示M71轴突纤维可以绕过定义其目标区域的Nrp1信号,因为它们被劫持并与靶向N别处的Nrp1缺失的M71表达轴突结合。在一起,这些发现显示完全不同的轴突靶向结果取决于Nrp1 / Sema3A信号改变的时间。

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