Department of Physiological Sciences, University of Catania, Catania, Italy.
Eur J Neurosci. 2010 Apr;31(8):1423-34. doi: 10.1111/j.1460-9568.2010.07170.x. Epub 2010 Apr 9.
Recent studies have attempted to repair the damaged spinal cord (SC) by stimulating neurogenesis or neuroplasticity. Sonic hedgehog (Shh), Notch-1 and Numb are involved in the stem cell functioning. Additionally, Notch-1 has a role as modulator of synaptic plasticity. However, little is known about the role of these proteins in the adult SC after removal of motoneurons. In this study, we have injected cholera toxin-B saporin into the gastrocnemius muscle to induce a depletion of motoneurons within the lumbar SC of adult mice, and analysed the expression of choline acetyltransferase (ChAT), Synapsin-I, Shh, Notch-1 and Numb proteins. The functional outcome of the lesion was monitored by grid walk and rotarod tasks. The neurotoxin lesion determined a motoneuron depletion and a transient decrease of ChAT, Synapsin-I, Shh and Numb levels in the lumbar SC. ChAT was associated with Synapsin-I expression and motor performance at 1 week but not 1 month after lesion, suggesting that the recovery of locomotion could depend on synaptic plasticity, at least in an early phase. Shh and Notch-1 were associated with Synapsin-I levels, suggesting a role in modulating synaptic plasticity. Numb expression also appeared reduced after lesion and linked to motor performance. Moreover, unlike other lesion models, we observed glial reaction but no evidence of cell proliferation within the depleted SC. Given the mentioned roles of Shh, Notch-1 and Numb, we believe that an in vivo manipulation of their signalling after lesion could represent a suitable way to improve functional recovery by modulating synaptic plasticity and/or neurogenesis.
最近的研究试图通过刺激神经发生或神经可塑性来修复受损的脊髓 (SC)。 Sonic hedgehog (Shh)、Notch-1 和 Numb 参与了干细胞的功能。此外,Notch-1 作为突触可塑性的调节剂发挥作用。然而,关于这些蛋白质在去除运动神经元后成年 SC 中的作用知之甚少。在这项研究中,我们将霍乱毒素 B 链霉素注入比目鱼肌,以诱导成年小鼠腰 SC 中的运动神经元耗竭,并分析胆碱乙酰转移酶 (ChAT)、突触素-I、Shh、Notch-1 和 Numb 蛋白的表达。通过网格行走和转棒任务监测损伤的功能结果。神经毒素损伤导致运动神经元耗竭和 ChAT、突触素-I、Shh 和 Numb 水平在腰 SC 中的短暂下降。ChAT 与突触素-I 的表达和运动表现相关,在损伤后 1 周而非 1 个月,但这表明运动功能的恢复可能依赖于突触可塑性,至少在早期阶段如此。Shh 和 Notch-1 与突触素-I 水平相关,表明其在调节突触可塑性方面发挥作用。Numb 的表达在损伤后也似乎降低,并与运动表现相关。此外,与其他损伤模型不同,我们观察到胶质细胞反应,但在耗竭的 SC 中没有细胞增殖的证据。鉴于 Shh、Notch-1 和 Numb 的上述作用,我们认为在损伤后对其信号通路进行体内操纵可能是通过调节突触可塑性和/或神经发生来改善功能恢复的一种合适方法。