Klymenko Andrii, Lutz David
Department of Neuroanatomy and Molecular Brain Research, Ruhr University Bochum, Bochum, Germany.
Front Cell Dev Biol. 2022 Oct 10;10:999322. doi: 10.3389/fcell.2022.999322. eCollection 2022.
It has widely been thought that in the process of nerve regeneration Schwann cells populate the injury site with myelinating, non-myelinating, phagocytic, repair, and mesenchyme-like phenotypes. It is now clear that the Schwann cells modify their shape and basal lamina as to accommodate re-growing axons, at the same time clear myelin debris generated upon injury, and regulate expression of extracellular matrix proteins at and around the lesion site. Such a remarkable plasticity may follow an intrinsic functional rhythm or a systemic circadian clock matching the demands of accurate timing and precision of signalling cascades in the regenerating nervous system. Schwann cells react to changes in the external circadian clock clues and to the Zeitgeber hormone melatonin by altering their plasticity. This raises the question of whether melatonin regulates Schwann cell activity during neurorepair and if circadian control and rhythmicity of Schwann cell functions are vital aspects of neuroregeneration. Here, we have focused on different schools of thought and emerging concepts of melatonin-mediated signalling in Schwann cells underlying peripheral nerve regeneration and discuss circadian rhythmicity as a possible component of neurorepair.
人们普遍认为,在神经再生过程中,施万细胞以髓鞘形成、非髓鞘形成、吞噬、修复和间充质样表型填充损伤部位。现在很清楚的是,施万细胞会改变其形状和基膜,以适应再生的轴突,同时清除损伤时产生的髓鞘碎片,并调节损伤部位及其周围细胞外基质蛋白的表达。这种显著的可塑性可能遵循内在的功能节律或与再生神经系统中信号级联的精确时间和精度需求相匹配的系统生物钟。施万细胞通过改变其可塑性来对外在生物钟线索的变化和授时因子褪黑素做出反应。这就提出了一个问题,即褪黑素在神经修复过程中是否调节施万细胞的活性,以及施万细胞功能的昼夜节律控制和节律性是否是神经再生的重要方面。在这里,我们关注了关于外周神经再生中施万细胞内褪黑素介导信号传导的不同思想流派和新兴概念,并讨论了昼夜节律性作为神经修复的一个可能组成部分。