Department of Immunology, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, Kawaramachi Hirokoji Kajii-cho 465, Kamigyo-ku, Kyoto, 602-8566, Japan.
Department of Plastic and Reconstructive Surgery, Graduate School of Medical Sciences, Kyoto Prefectural University of Medicine, Kawaramachi Hirokoji Kajii-cho 465, Kamigyo-ku, Kyoto, 602-8566, Japan.
Stem Cells Transl Med. 2017 Apr;6(4):1207-1216. doi: 10.1002/sctm.16-0122. Epub 2017 Jan 9.
Schwann cells (SCs) play pivotal roles in the maintenance and regeneration of the peripheral nervous system. Although transplantation of SCs enhances repair of experimentally damaged peripheral and central nerve tissues, it is difficult to prepare a sufficient number of functional SCs for transplantation therapy without causing adverse events for the donor. Here, we generated functional SCs by somatic cell reprogramming procedures and demonstrated their capability to promote peripheral nerve regeneration. Normal human fibroblasts were phenotypically converted into SCs by transducing SOX10 and Krox20 genes followed by culturing for 10 days resulting in approximately 43% directly converted Schwann cells (dSCs). The dSCs expressed SC-specific proteins, secreted neurotrophic factors, and induced neuronal cells to extend neurites. The dSCs also displayed myelin-forming capability both in vitro and in vivo. Moreover, transplantation of the dSCs into the transected sciatic nerve in mice resulted in significantly accelerated regeneration of the nerve and in improved motor function at a level comparable to that with transplantation of the SCs obtained from a peripheral nerve. The dSCs induced by our procedure may be applicable for novel regeneration therapy for not only peripheral nerve injury but also for central nerve damage and for neurodegenerative disorders related to SC dysfunction. Stem Cells Translational Medicine 2017;6:1207-1216.
许旺细胞(SCs)在外周神经系统的维持和再生中起着关键作用。虽然SCs 的移植增强了实验性损伤的周围和中枢神经组织的修复,但如果不引起供体的不良反应,很难制备足够数量的功能性SCs 用于移植治疗。在这里,我们通过体细胞重编程程序生成功能性SCs,并证明了它们促进周围神经再生的能力。正常的人成纤维细胞通过转导 SOX10 和 Krox20 基因,然后培养 10 天,表型转化为大约 43%的直接转化 Schwann 细胞(dSCs)。dSCs 表达 SC 特异性蛋白,分泌神经营养因子,并诱导神经元细胞伸出轴突。dSCs 还表现出体外和体内的髓鞘形成能力。此外,将 dSCs 移植到小鼠的横断坐骨神经中,可显著加速神经的再生,并改善运动功能,达到与从周围神经获得的SCs 移植相当的水平。我们的方法诱导的 dSCs 可能适用于不仅外周神经损伤,而且还适用于中枢神经损伤和与SCs 功能障碍相关的神经退行性疾病的新型再生治疗。《干细胞转化医学》2017;6:1207-1216。