首页> 外文期刊>Molecular and cellular neurosciences >Pontocerebellar Axon Guidance: Neuropilin-1- and Semaphorin 3A-Sensitivity Gradients across Basilar Pontine Nuclei and Semaphorin 3A Variation across Cerebellum.
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Pontocerebellar Axon Guidance: Neuropilin-1- and Semaphorin 3A-Sensitivity Gradients across Basilar Pontine Nuclei and Semaphorin 3A Variation across Cerebellum.

机译:桥小脑轴突指导:跨基底桥桥神经核的Neuropilin-1和Semaphorin 3A敏感性梯度和小脑的Semaphorin 3A变异。

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摘要

To assess the role of semaphorin 3A (Sema3A) and its receptor component neuropilin-1 (Npn-1) in pontocerebellar axon guidance, we compared the distributions of Sema3A, Npn-1, and DiI-labeled pontocerebellar axons in neonatal mouse cerebellum. Between embryonic day 18 and birth there was a large increase in Npn-1 expression in the basilar pontine nuclei (BPN), the major source of pontocerebellar axons. Sema3A expression in cerebellum also increased at this time. In the BPN, Npn-1 and the response of axons to Sema3A were graded with high Npn-1 and Sema3A responsiveness rostrally and lower levels caudally. The Npn-1 gradient was not smooth and cells with higher and lower expression were interspersed. Between birth and postnatal day 5, pontocerebellar axons projected to lobules of the hemispheres, including those with low to moderate levels of Sema3A, but did not enter regions with high levels of Sema3A, including the flocculus and much of the vermis. These results suggest that varying neuropilin levels on BPN axons, which correlated with their varying responses to Sema3A, combined with varying Sema3A levels across cerebellum, may contribute to guiding subsets of BPN axons to their distinct target regions within cerebellum.
机译:为了评估信号量3A(Sema3A)及其受体成分Neuropilin-1(Npn-1)在桥小脑轴突指导中的作用,我们比较了Sema3A,Npn-1和DiI标记的桥小脑轴突在新生小鼠小脑中的分布。在胚胎第18天到出生之间,基底桥脑桥核(BPN)是桥脑小脑轴突的主要来源,Npn-1表达大幅增加。此时小脑中Sema3A的表达也增加了。在BPN中,Npn-1和轴突对Sema3A的反应被分级为高Npn-1和Sema3A的反应性在尾端较高,而在尾端则较低。 Npn-1梯度不平滑,并且散布了具有较高和较低表达的细胞。在出生和出生后第5天之间,小脑轴突投射到半球小叶,包括Sema3A水平低至中度的小叶,但没有进入Sema3A水平高的区域,包括絮状体和许多ver骨。这些结果表明,BPN轴突上神经pil蛋白水平的变化与它们对Sema3A的不同反应相关,再加上小脑中Sema3A水平的变化,可能有助于将BPN轴突的子集引导至小脑内不同的靶区域。

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