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通过信号素-1a/丛状蛋白A介导的轴突-轴突相互作用对嗅觉受体神经元进行时间靶点限制。

Temporal target restriction of olfactory receptor neurons by Semaphorin-1a/PlexinA-mediated axon-axon interactions.

作者信息

Sweeney Lora B, Couto Africa, Chou Ya-Hui, Berdnik Daniela, Dickson Barry J, Luo Liqun, Komiyama Takaki

机构信息

Howard Hughes Medical Institute, Department of Biological Sciences and Neurosciences Program, Stanford University, Stanford, CA 94305, USA.

出版信息

Neuron. 2007 Jan 18;53(2):185-200. doi: 10.1016/j.neuron.2006.12.022.

Abstract

Axon-axon interactions have been implicated in neural circuit assembly, but the underlying mechanisms are poorly understood. Here, we show that in the Drosophila antennal lobe, early-arriving axons of olfactory receptor neurons (ORNs) from the antenna are required for the proper targeting of late-arriving ORN axons from the maxillary palp (MP). Semaphorin-1a is required for targeting of all MP but only half of the antennal ORN classes examined. Sema-1a acts nonautonomously to control ORN axon-axon interactions, in contrast to its cell-autonomous function in olfactory projection neurons. Phenotypic and genetic interaction analyses implicate PlexinA as the Sema-1a receptor in ORN targeting. Sema-1a on antennal ORN axons is required for correct targeting of MP axons within the antennal lobe, while interactions amongst MP axons facilitate their entry into the antennal lobe. We propose that Sema-1a/PlexinA-mediated repulsion provides a mechanism by which early-arriving ORN axons constrain the target choices of late-arriving axons.

摘要

轴突-轴突相互作用与神经回路组装有关,但其潜在机制仍知之甚少。在这里,我们表明,在果蝇触角叶中,来自触角的嗅觉受体神经元(ORN)的早期到达轴突是上颌触须(MP)的晚期到达ORN轴突正确靶向所必需的。信号素-1a是所有MP轴突靶向所必需的,但在所检查的触角ORN类别中只有一半需要它。与信号素-1a在嗅觉投射神经元中的细胞自主功能相反,它以非自主方式控制ORN轴突-轴突相互作用。表型和遗传相互作用分析表明,在ORN靶向中,丛状蛋白A是信号素-1a的受体。触角ORN轴突上的信号素-1a是MP轴突在触角叶内正确靶向所必需的,而MP轴突之间的相互作用促进它们进入触角叶。我们提出,信号素-1a/丛状蛋白A介导的排斥作用提供了一种机制,通过该机制,早期到达的ORN轴突限制了晚期到达轴突的目标选择。

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