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阻断骨骼肌 DHPRs/Ryr1 可防止 III 型神经调节蛋白 1(CRD-Nrg1)缺乏型突变小鼠的神经肌肉突触丢失。

Blocking skeletal muscle DHPRs/Ryr1 prevents neuromuscular synapse loss in mutant mice deficient in type III Neuregulin 1 (CRD-Nrg1).

机构信息

Department of Neuroscience, UT Southwestern Medical Center, Dallas, United States of America.

The Salk Institute, La Jolla, United States of America.

出版信息

PLoS Genet. 2019 Mar 14;15(3):e1007857. doi: 10.1371/journal.pgen.1007857. eCollection 2019 Mar.

Abstract

Schwann cells are integral components of vertebrate neuromuscular synapses; in their absence, pre-synaptic nerve terminals withdraw from post-synaptic muscles, leading to muscle denervation and synapse loss at the developing neuromuscular junction (NMJ). Here, we report a rescue of muscle denervation and neuromuscular synapses loss in type III Neuregulin 1 mutant mice (CRD-Nrg1-/-), which lack Schwann cells. We found that muscle denervation and neuromuscular synapse loss were prevented in CRD-Nrg1-/-mice when presynaptic activity was blocked by ablating a specific gene, such as Snap25 (synaptosomal-associated 25 kDa protein) or Chat (choline acetyltransferase). Further, these effects were mediated by a pathway that requires postsynaptic acetylcholine receptors (AChRs), because ablating Chrna1 (acetylcholine receptor α1 subunit), which encodes muscle-specific AChRs in CRD-Nrg1-/-mice also rescued muscle denervation. Moreover, genetically ablating muscle dihydropyridine receptor (DHPR) β1 subunit (Cacnb1) or ryanodine receptor 1 (Ryr1) also rescued muscle denervation and neuromuscular synapse loss in CRD-Nrg1-/-mice. Thus, these genetic manipulations follow a pathway-from presynaptic to postsynaptic, and, ultimately to muscle activity mediated by DHPRs and Ryr1. Importantly, electrophysiological analyses reveal robust synaptic activity in the rescued, Schwann-cell deficient NMJs in CRD-Nrg1-/-Cacnb1-/-or CRD-Nrg1-/-Ryr1-/-mutant mice. Thus, a blockade of synaptic activity, although sufficient, is not necessary to preserve NMJs that lack Schwann cells. Instead, a blockade of muscle activity mediated by DHRPs and Ryr1 is both necessary and sufficient for preserving NMJs that lack Schwann cells. These findings suggest that muscle activity mediated by DHPRs/Ryr1 may destabilize developing NMJs and that Schwann cells play crucial roles in counteracting such a destabilizing activity to preserve neuromuscular synapses during development.

摘要

施万细胞是脊椎动物神经肌肉突触的组成部分;在它们缺失的情况下,前突触神经末梢从后突触肌肉中撤出,导致肌肉去神经和发育中的神经肌肉接点(NMJ)处的突触丢失。在这里,我们报告了一种对缺乏施万细胞的 III 型神经调节蛋白 1 突变小鼠(CRD-Nrg1-/-)的肌肉去神经和神经肌肉突触丢失的挽救。我们发现,当通过消融特定基因(如 Snap25(突触相关 25kDa 蛋白)或 Chat(胆碱乙酰转移酶))阻断突触前活性时,CRD-Nrg1-/-小鼠的肌肉去神经和神经肌肉突触丢失得到了预防。此外,这些作用是通过一条需要突触后乙酰胆碱受体(AChRs)的途径介导的,因为在 CRD-Nrg1-/-小鼠中消融编码肌肉特异性 AChRs 的 Chrna1(乙酰胆碱受体α1 亚单位)也挽救了肌肉去神经。此外,通过遗传消融肌肉二氢吡啶受体(DHPR)β1 亚基(Cacnb1)或 Ryanodine 受体 1(Ryr1)也挽救了 CRD-Nrg1-/-小鼠的肌肉去神经和神经肌肉突触丢失。因此,这些遗传操作遵循一条从突触前到突触后,最终到由 DHPRs 和 Ryr1 介导的肌肉活动的途径。重要的是,电生理分析显示在 CRD-Nrg1-/-Cacnb1-/-或 CRD-Nrg1-/-Ryr1-/-突变小鼠中,受挽救的缺乏施万细胞的 NMJ 具有强大的突触活性。因此,尽管抑制突触活动是足够的,但对于保留缺乏施万细胞的 NMJ 并不是必需的。相反,DHPRs 和 Ryr1 介导的肌肉活动的阻断对于保留缺乏施万细胞的 NMJ 既是必需的,也是充分的。这些发现表明,DHPRs/Ryr1 介导的肌肉活动可能会使发育中的 NMJ 不稳定,而施万细胞在发育过程中通过拮抗这种不稳定活性来保护神经肌肉突触方面发挥着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cb8/6417856/8250f080342d/pgen.1007857.g001.jpg

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