Shurin Michael R, Wheeler Sarah E, Zhong Hua, Zhou Yan
Division of Clinical Immunopathology, Department of Pathology, University of Pittsburgh and University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Department of Respiratory and Critical Care Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Cells. 2025 Aug 28;14(17):1336. doi: 10.3390/cells14171336.
Schwann cells (SCs) are the primary glial cells of the Peripheral Nervous System (PNS), which insulate and provide protection and nutrients to the axons. Technological and experimental advances in neuroscience, focusing on the biology of SCs, their interactions with other cells, and their role in the pathogenesis of various diseases, have paved the way for exploring new treatment strategies that aim to harness the direct protective or causative properties of SCs in neurological disorders. SCs express cytokines, chemokines, neurotrophic growth factors, matrix metalloproteinases, extracellular matrix proteins, and extracellular vesicles, which promote the inherent potential of the injured neurons to survive and accelerate axonal elongation. The ability of SCs to support the development and functioning of neurons is lost in certain hereditary, autoimmune, metabolic, traumatic, and toxic conditions, suggesting their role in specific neurological diseases. Thus, targeting, modifying, and replacing SC strategies, as well as utilizing SC-derived factors and exosomes, have been considered novel therapeutic opportunities for neuropathological conditions. Preclinical and clinical data have demonstrated that SCs and SC-derived factors can serve as viable cell therapy for reconstructing the local tissue microenvironment and promoting nerve anatomical and functional recovery in both peripheral and central nerve injury repair, as well as in peripheral neuropathies. However, despite the promising successes of genetic engineering of SCs, which are now in preclinical and clinical trials, improving tactics to obtain 'repair' SCs and their products from different sources is the key goal for future clinical success. Finally, further development of innovative therapeutic approaches to target and modify SC survival and function in vivo is also urgently needed.
施万细胞(SCs)是周围神经系统(PNS)的主要神经胶质细胞,它为轴突提供绝缘、保护和营养。神经科学领域的技术和实验进展聚焦于施万细胞的生物学特性、它们与其他细胞的相互作用以及它们在各种疾病发病机制中的作用,为探索新的治疗策略铺平了道路,这些策略旨在利用施万细胞在神经系统疾病中的直接保护或致病特性。施万细胞表达细胞因子、趋化因子、神经营养生长因子、基质金属蛋白酶、细胞外基质蛋白和细胞外囊泡,这些物质可促进受损神经元存活的内在潜能并加速轴突伸长。在某些遗传性、自身免疫性、代谢性、创伤性和中毒性疾病中,施万细胞支持神经元发育和功能的能力会丧失,这表明它们在特定神经系统疾病中发挥作用。因此,靶向、修饰和替代施万细胞的策略,以及利用施万细胞衍生的因子和外泌体,已被视为神经病理状况的新型治疗机会。临床前和临床数据表明,施万细胞和施万细胞衍生的因子可作为可行的细胞疗法,用于重建局部组织微环境,并促进周围和中枢神经损伤修复以及周围神经病变中的神经解剖和功能恢复。然而,尽管施万细胞基因工程在临床前和临床试验中取得了令人鼓舞的成功,但改进从不同来源获取“修复性”施万细胞及其产物的策略是未来临床成功的关键目标。最后,迫切需要进一步开发创新的治疗方法,以在体内靶向和修饰施万细胞的存活和功能。