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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >A RET-ER81-NRG1 Signaling Pathway Drives the Development of Pacinian Corpuscles
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A RET-ER81-NRG1 Signaling Pathway Drives the Development of Pacinian Corpuscles

机译:RET-ER81-NRG1信号通路驱动帕西尼亚小体的发育

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摘要

Axon-Schwann cell interactions are crucial for the development, function, and repair of the peripheral nervous system, but mechanisms underlying communication between axons and nonmyelinating Schwann cells are unclear. Here, we show that ER81 is functionally required in a subset of mouse RET+ mechanosensory neurons for formation of Pacinian corpuscles, which are composed of a single myelinated axon and multiple layers of nonmyelinating Schwann cells, and Ret is required for the maintenance of Er81 expression. Interestingly, Er81 mutants have normal myelination but exhibit deficient interactions between axons and corpuscle-forming nonmyelinating Schwann cells. Finally, ablating Neuregulin-1 (Nrg1) in mechanosensory neurons results in no Pacinian corpuscles, and an Nrg1 isoform not required for communication with myelinating Schwann cells is specifically decreased in Er81-null somatosensory neurons. Collectively, our results suggest that a RET-ER81-NRG1 signaling pathway promotes axon communication with nonmyelinating Schwann cells, and that neurons use distinct mechanisms to interact with different types of Schwann cells.
机译:轴突-施万细胞相互作用对周围神经系统的发育,功能和修复至关重要,但轴突与非髓鞘雪旺细胞之间的通讯机制尚不清楚。在这里,我们显示ER81在小鼠RET +机械感觉神经元的子集中需要功能,以形成Pacinian小体,该小体由单个髓鞘轴突和多层非髓鞘雪旺细胞组成,而Ret是维持Er81表达所需的。有趣的是,Er81突变体的髓鞘形成正常,但在轴突和形成小体的非髓鞘雪旺细胞之间显示出不足的相互作用。最后,在机械感觉神经元中切除Neuregulin-1(Nrg1)不会导致Pacinian小体,并且在Er81-null的体感神经元中,与髓鞘雪旺细胞通讯所不需要的Nrg1亚型特别降低。总的来说,我们的研究结果表明,RET-ER81-NRG1信号通路促进了与非髓鞘雪旺细胞的轴突通讯,并且神经元使用不同的机制与不同类型的雪旺细胞相互作用。

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