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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.>SIGNIFICANCE STATEMENT Communication between neurons and Schwann cells is critical for development, normal function, and regeneration of the peripheral nervous system. Despite many studies about axonal communication with myelinating Schwann cells, mostly via a specific isoform of Neuregulin1, the molecular nature of axonal communication with nonmyelinating Schwann cells is poorly understood. Here, we described a RET-ER81-Neuregulin1 signaling pathway in neurons innervating Pacinian corpuscle somatosensory end organs, which is essential for communication between the innervating axon and the end organ nonmyelinating Schwann cells. We also showed that this signaling pathway uses isoforms of Neuregulin1 that are not involved in myelination, providing evidence that neurons use different isoforms of Neuregulin1 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,但是尚不清楚轴突与非髓鞘雪旺细胞之间通信的基础机制。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,Ret为维持Er81表达所需。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。总体而言,我们的研究结果表明,RET-ER81-NRG1信号通路可促进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。>意义声明雪旺氏细胞对于周围神经系统的发育,正常功能和再生至关重要。尽管有很多关于髓鞘雪旺细胞与轴突通讯的研究,主要是通过特定的神经调节蛋白亚型,但人们对轴突细胞与非髓鞘雪旺细胞的分子性质了解甚少。在这里,我们描述了神经系统神经元中的RET-ER81-Neuregulin1信号通路,神经系统支配Pacinian小体体感末端器官,这对于支配神经轴突与末端器官非髓鞘雪旺细胞之间的通信至关重要。我们还表明,该信号传导途径使用了不参与髓鞘形成的神经调节蛋白亚型,提供了神经元使用神经调节蛋白1的不同亚型与不同类型的雪旺氏细胞相互作用的证据。

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