Wang Hong-Tao, Li Yi-Zhe, Fu Qi-Ran, Zhang Meng-Yi, Li Hu
School of Life Science and Technology, Xinxiang Medical University, Xinxiang 453003, China.
School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang 453003, China.
Sheng Li Xue Bao. 2019 Aug 25;71(4):597-603.
Central nervous system injury leads to irreversible neuronal loss and glial scar formation, which ultimately results in persistent neurological dysfunction. Regenerative medicine suggests that replenishing missing neurons may be an ideal approach to repair the damage. Recent researches showed that many mature cells could be transdifferentiated into functional neurons by reprogramming. Therefore, reprogramming endogenous glia in situ to produce functional neurons shows great potential and unique advantage for repairing neuronal damage and treating neurodegenerative diseases. The present review summarized the current research progress on in situ transdifferentiation in the central nervous system, focusing on the cell types, characteristics and research progress of glial cells that could be transdifferentiated in situ, in order to provide theoretical basis for the development of new therapeutic strategies of neuronal injury and further clinical application.
中枢神经系统损伤会导致不可逆的神经元丢失和胶质瘢痕形成,最终导致持续的神经功能障碍。再生医学表明,补充缺失的神经元可能是修复损伤的理想方法。最近的研究表明,许多成熟细胞可以通过重编程转分化为功能性神经元。因此,原位重编程内源性胶质细胞以产生功能性神经元在修复神经元损伤和治疗神经退行性疾病方面具有巨大潜力和独特优势。本综述总结了中枢神经系统原位转分化的当前研究进展,重点关注可原位转分化的胶质细胞的细胞类型、特征和研究进展,为开发神经元损伤的新治疗策略及进一步的临床应用提供理论依据。