School of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
Mol Neurobiol. 2024 Feb;61(2):935-949. doi: 10.1007/s12035-023-03613-3. Epub 2023 Sep 6.
Although the benefits of electroacupuncture (EA) for peripheral nerve injury (PNI) are well accepted in clinical practice, the underlying mechanism remains incompletely elucidated. In our study, we observed that EA intervention led to a reduction in the expression of the long non-coding RNA growth-arrest-specific transcript 5 (GAS5) and an increased in miR-21 levels within the injured nerve, effectively promoting functional recovery and nerve regeneration following sciatic nerve injury (SNI). In contrast, administration of adeno-associated virus expressing GAS5 (AAV-GAS5) weakened the therapeutic effect of EA. On the other hand, both silencing GAS5 and introducing a miR-21 mimic prominently enhanced the proliferation activity and migration ability of Schwann cells (SCs), while also inhibiting SCs apoptosis. On the contrary, inhibition of SCs apoptosis was found to be mediated by miR-21. Additionally, overexpression of GAS5 counteracted the effects of the miR-21 mimic on SCs. Moreover, SCs that transfected with the miR-21 mimic promoted neurite growth in hypoxia/reoxygenation-induced neurons, which might be prevented by overexpressing GAS5. Furthermore, GAS5 was found to be widely distributed in the cytoplasm and was negatively regulated by miR-21. Consequently, the targeting of GAS5 by miR-21 represents a potential mechanism through which EA enhances reinnervation and functional restoration following SNI. Mechanistically, the GAS5/miR-21 axis can modulate the proliferation, migration, and apoptosis of SCs while potentially influencing the neurite growth of neurons.
尽管电针(EA)在周围神经损伤(PNI)的临床应用中具有显著疗效,但其潜在机制仍不完全清楚。在我们的研究中,我们观察到 EA 干预导致损伤神经内长链非编码 RNA 生长停滞特异性转录物 5(GAS5)的表达减少,miR-21 水平升高,有效促进坐骨神经损伤(SNI)后功能恢复和神经再生。相反,给予表达 GAS5 的腺相关病毒(AAV-GAS5)减弱了 EA 的治疗效果。另一方面,沉默 GAS5 和引入 miR-21 模拟物均可显著增强施万细胞(SCs)的增殖活性和迁移能力,同时抑制 SCs 凋亡。相反,miR-21 介导了 SCs 凋亡的抑制。此外,GAS5 的过表达拮抗了 miR-21 模拟物对 SCs 的作用。此外,转染 miR-21 模拟物的 SCs 促进了缺氧/复氧诱导神经元中的轴突生长,而过表达 GAS5 可能会阻止这种作用。此外,GAS5 在细胞质中广泛分布,并受 miR-21 的负调控。因此,miR-21 靶向 GAS5 可能是 EA 增强 SNI 后神经再支配和功能恢复的潜在机制。从机制上讲,GAS5/miR-21 轴可调节 SCs 的增殖、迁移和凋亡,并可能影响神经元的轴突生长。