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内源性神经干细胞具有潜伏的谱系分化潜能,可促进脊髓损伤修复。

A latent lineage potential in resident neural stem cells enables spinal cord repair.

机构信息

Department of Cell and Molecular Biology, Karolinska Institutet, SE-171 77 Stockholm, Sweden.

Department of Neuroscience, Karolinska Institutet, SE-171 77 Stockholm, Sweden.

出版信息

Science. 2020 Oct 2;370(6512). doi: 10.1126/science.abb8795.

Abstract

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.

摘要

中枢神经系统 (CNS) 的损伤修复效率低下。内源性神经干细胞对细胞替代的贡献有限。我们发现神经干细胞具有潜在的能力,可以在受伤的小鼠脊髓中大量替代丢失的少突胶质细胞。通过整合多模态单细胞分析,我们发现神经干细胞处于一种允许其展开正常潜伏的少突胶质细胞发生基因表达程序的开放染色质状态。转录因子 OLIG2 的异位表达揭示了丰富的干细胞源性少突胶质细胞发生,其遵循少突胶质细胞分化的自然进程,有助于轴突髓鞘再生,并刺激轴突传导功能的恢复。因此,在中枢神经系统损伤后,招募内源性干细胞可能成为细胞移植的替代方法。

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