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许旺细胞在神经再生选择性中的作用。

Schwann Cell Role in Selectivity of Nerve Regeneration.

机构信息

Institute of Neurosciences, Department Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 08193 Bellaterra, Spain.

出版信息

Cells. 2020 Sep 20;9(9):2131. doi: 10.3390/cells9092131.

Abstract

Peripheral nerve injuries result in the loss of the motor, sensory and autonomic functions of the denervated segments of the body. Neurons can regenerate after peripheral axotomy, but inaccuracy in reinnervation causes a permanent loss of function that impairs complete recovery. Thus, understanding how regenerating axons respond to their environment and direct their growth is essential to improve the functional outcome of patients with nerve lesions. Schwann cells (SCs) play a crucial role in the regeneration process, but little is known about their contribution to specific reinnervation. Here, we review the mechanisms by which SCs can differentially influence the regeneration of motor and sensory axons. Mature SCs express modality-specific phenotypes that have been associated with the promotion of selective regeneration. These include molecular markers, such as L2/HNK-1 carbohydrate, which is differentially expressed in motor and sensory SCs, or the neurotrophic profile after denervation, which differs remarkably between SC modalities. Other important factors include several molecules implicated in axon-SC interaction. This cell-cell communication through adhesion (e.g., polysialic acid) and inhibitory molecules (e.g., MAG) contributes to guiding growing axons to their targets. As many of these factors can be modulated, further research will allow the design of new strategies to improve functional recovery after peripheral nerve injuries.

摘要

周围神经损伤导致去神经支配节段的运动、感觉和自主功能丧失。神经元在周围轴突切断后可以再生,但神经再支配的不准确会导致功能永久丧失,从而阻碍完全恢复。因此,了解再生轴突如何对其环境做出反应并指导其生长对于改善神经损伤患者的功能预后至关重要。施万细胞 (SCs) 在再生过程中起着至关重要的作用,但对其对特定再支配的贡献知之甚少。在这里,我们回顾了 SCs 可以差异化影响运动和感觉轴突再生的机制。成熟的 SCs 表达特定模式的表型,这些表型与促进选择性再生有关。这些包括分子标志物,例如 L2/HNK-1 碳水化合物,它在运动和感觉 SCs 中表达不同,或去神经支配后神经营养谱显著不同。其他重要因素包括几种涉及轴突-SC 相互作用的分子。这种细胞间的通讯通过黏附(例如,多唾液酸)和抑制分子(例如,MAG)来指导生长轴突到达其靶标。由于许多这些因素可以被调节,进一步的研究将允许设计新的策略来改善周围神经损伤后的功能恢复。

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