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延迟周围神经修复后小鼠神经再生后靶肌肉中神经肌肉接头的重塑。

Remodeling of Neuromuscular Junctions in Target Muscle Following Nerve Regeneration in Mice After Delayed Peripheral Nerve Repair.

机构信息

Department of Orthopaedic and Spinal Surgery, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima Bunkyo, Tokyo 113-8519, Japan; Department of Traumatic Orthopaedics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

Department of Orthopaedic and Spinal Surgery, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima Bunkyo, Tokyo 113-8519, Japan.

出版信息

Neuroscience. 2023 Aug 1;524:197-208. doi: 10.1016/j.neuroscience.2023.05.008. Epub 2023 May 17.

Abstract

Peripheral nerve injury (PNI) induces severe functional loss in extremities. Progressive denervation and atrophy occur in the muscles if the nerve repair is delayed for long periods of the time. To overcome these difficulties, detailed mechanisms should be determined for neuromuscular junction (NMJ) degeneration in target muscles after PNI and regeneration after nerve repair. We established two models of end-to-end neurorrhaphy and allogeneic nerve grafting in the chronic phase after common peroneal nerve injury in female mice (n = 100 in total). We evaluated motor function, histology, and gene expression in the target muscles during their regeneration processes and compared the models. We found that the functional recovery with allogeneic nerve grafting was superior to that with end-to-end neurorrhaphy, and the number of reinnervated NMJs and Schwann cells was increased at 12 weeks after allograft. In addition, NMJ- and Schwann cell-related molecules showed high expression in the target muscle in the allograft model. These results suggest that Schwann cell migrating from the allograft might play a crucial role in nerve regeneration in the chronic phase after PNI. The relationship between the NMJ and Schwann cells should be further investigated in the target muscle.

摘要

周围神经损伤(PNI)会导致四肢严重的功能丧失。如果神经修复延迟很长时间,肌肉会出现进行性去神经和萎缩。为了克服这些困难,应该确定 PNI 后靶肌肉中的神经肌肉接头(NMJ)退化和神经修复后的再生的详细机制。我们在雌性小鼠的坐骨神经损伤后慢性期建立了端端神经吻合和同种异体神经移植的两种模型(总共 100 只)。我们在再生过程中评估了靶肌肉的运动功能、组织学和基因表达,并比较了两种模型。我们发现,同种异体神经移植的功能恢复优于端端神经吻合,并且在同种异体移植后 12 周,再支配的 NMJ 和施万细胞数量增加。此外,NMJ 和施万细胞相关分子在同种异体移植模型中的靶肌肉中表达较高。这些结果表明,从同种异体移植物中迁移的施万细胞可能在 PNI 后慢性期的神经再生中发挥关键作用。应进一步研究 NMJ 和施万细胞之间的关系。

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