1 Waisman Center, University of Wisconsin-Madison, Madison, WI, USA.
2 Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
Neuroscientist. 2018 Dec;24(6):627-638. doi: 10.1177/1073858417751112. Epub 2018 Jan 7.
The journey of Schwann cells from their origin in the neural crest to their ensheathment and myelination of peripheral nerves is a remarkable one. Their apparent static function in enabling saltatory conduction of mature nerve is not only vital for long-term health of peripheral nerve but also belies an innate capacity of terminally differentiated Schwann cells to radically alter their differentiation status in the face of nerve injury. The transition from migrating neural crest cells to nerve ensheathment, and then myelination of large diameter axons has been characterized extensively and several of the transcriptional networks have been identified. However, transcription factors must also modify chromatin structure during Schwann cell maturation and this review will focus on chromatin modification machinery that is involved in promoting the transition to, and maintenance of, myelinating Schwann cells. In addition, Schwann cells are known to play important regenerative roles after peripheral nerve injury, and information on epigenomic reprogramming of the Schwann cell genome has emerged. Characterization of epigenomic requirements for myelin maintenance and Schwann cell responses to injury will be vital in understanding how the various Schwann cell functions can be optimized to maintain and repair peripheral nerve function.
许旺细胞从神经嵴起源到外周神经的包绕和髓鞘形成的旅程是非常了不起的。它们在成熟神经的跳跃传导中发挥的明显静态功能,不仅对周围神经的长期健康至关重要,而且还掩盖了终末分化的许旺细胞在面对神经损伤时彻底改变其分化状态的固有能力。从迁移的神经嵴细胞到神经包绕,然后到大直径轴突的髓鞘形成,这一过程已经得到了广泛的描述,并且已经确定了几个转录网络。然而,转录因子也必须在许旺细胞成熟过程中修饰染色质结构,本综述将重点介绍参与促进向髓鞘形成许旺细胞的转变和维持的染色质修饰机制。此外,许旺细胞在外周神经损伤后已知发挥重要的再生作用,并且已经出现了许旺细胞基因组的表观基因组重编程信息。对髓鞘维持和许旺细胞对损伤反应的表观基因组要求的特征描述,对于理解如何优化各种许旺细胞功能以维持和修复周围神经功能至关重要。