室管膜细胞
神经干细胞
再髓鞘化
干细胞
奥利格2
生物
少突胶质细胞
神经科学
细胞生物学
轴突
脊髓损伤
脊髓
谱系(遗传)
髓鞘
中枢神经系统
基因
遗传学
作者
Enric Llorens-Bobadilla,James M. Chell,Pierre Le Merre,Yi‐Cheng Wu,Margherita Zamboni,Joseph Bergenstråhle,Moa Stenudd,Elena Sopova,Joakim Lundeberg,Oleg Shupliakov,Marie Carlén,Jonas Frisén
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-10-02
卷期号:370 (6512)
被引量:170
标识
DOI:10.1126/science.abb8795
摘要
Injuries to the central nervous system (CNS) are inefficiently repaired. Resident neural stem cells manifest a limited contribution to cell replacement. We have uncovered a latent potential in neural stem cells to replace large numbers of lost oligodendrocytes in the injured mouse spinal cord. Integrating multimodal single-cell analysis, we found that neural stem cells are in a permissive chromatin state that enables the unfolding of a normally latent gene expression program for oligodendrogenesis after injury. Ectopic expression of the transcription factor OLIG2 unveiled abundant stem cell-derived oligodendrogenesis, which followed the natural progression of oligodendrocyte differentiation, contributed to axon remyelination, and stimulated functional recovery of axon conduction. Recruitment of resident stem cells may thus serve as an alternative to cell transplantation after CNS injury.
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