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内耳中的施万细胞:发育、疾病与再生

Schwann cells in the inner ear: development, disease, and regeneration.

作者信息

Montigny Drew J, Kempfle Judith S

机构信息

Department of Otolaryngology, UMass Memorial Medical Center, Worcester, MA, United States.

University of Massachusetts Chan Medical School, Worcester, MA, United States.

出版信息

Front Cell Neurosci. 2025 Sep 10;19:1662274. doi: 10.3389/fncel.2025.1662274. eCollection 2025.

Abstract

Schwann cells are classically known as the constituent supporting cells of the peripheral nervous system. Beyond the scope of merely myelinating axons of the more saliently known neurons, Schwann cells comprise the majority of peripheral nervous system tissue. Through the lens of the inner ear, additional properties of Schwann cells are becoming elucidated. Therein, the process of myelin formation in development is more aptly understood as a homeostatic oscillation of differentiation status. Perpetual interaction between neural and non-neural cells of the inner ear maintains an intricate balance of guidance, growth, and maturation during development. In disease, aberration to Schwann cell myelination contributes to sensorineural hearing loss in conditions such as Guillain-Barre Syndrome and Charcot-Marie-Tooth disease, and tumorigenic over proliferation of Schwann cells defines vestibular schwannomas seen in neurofibromatosis type 2. Schwann cells demonstrate plasticity during oscillations between differentiation and dedifferentiation, a property that is now being leveraged in efforts to regenerate lost neurons. Emerging strategies of reprogramming, small molecule modulation, and gene therapy suggest that Schwann cells could serve as progenitor cells for regenerated neurons. Understanding the duality of Schwann cells in pathology and repair could transform the approach to treating sensorineural hearing loss.

摘要

施万细胞通常被认为是周围神经系统的组成性支持细胞。除了为更为人熟知的神经元的轴突形成髓鞘这一作用外,施万细胞构成了周围神经系统组织的大部分。通过内耳这个视角,施万细胞的其他特性正逐渐被阐明。在那里,发育过程中的髓鞘形成过程更恰当地被理解为分化状态的稳态振荡。内耳的神经细胞和非神经细胞之间的持续相互作用在发育过程中维持着引导、生长和成熟的复杂平衡。在疾病中,施万细胞髓鞘形成的异常会导致诸如吉兰 - 巴雷综合征和夏科 - 马里 - 图斯病等病症中的感音神经性听力损失,而施万细胞的致瘤性过度增殖则定义了2型神经纤维瘤病中所见的前庭神经鞘瘤。施万细胞在分化和去分化之间的振荡过程中表现出可塑性,这一特性目前正被用于再生丢失神经元的研究中。重编程、小分子调节和基因治疗等新兴策略表明,施万细胞可以作为再生神经元的祖细胞。了解施万细胞在病理和修复方面的双重性可能会改变感音神经性听力损失的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecf1/12457403/a3b2502b2fee/fncel-19-1662274-g0001.jpg

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