Neuronal activity-dependent myelin repair promotes motor function recovery after contusion spinal cord injury

被引:14
作者
Luo, Meiling [1 ]
Yin, Ying [1 ]
Li, Duanfang [2 ]
Tang, Weiwei [2 ]
Liu, Yuan [3 ]
Pan, Lu [1 ]
Yu, Lehua [1 ]
Tan, Botao [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 2, Dept Rehabil Med, Chongqing, Peoples R China
[2] Army Med Univ, Xinqiao Hosp, Dept Rehabil Med, Chongqing, Peoples R China
[3] Army Med Univ, Daping Hosp, Dept Res Inst Surg, State Key Lab Trauma Burns & Combined Injury, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
SCI; Neuronal activity; DREADDs; Remyelination; Oligodendrocyte lineage cells (OLs); motor function; NEURAL STEM-CELLS; REMYELINATION; CNS; DEMYELINATION; STIMULATION; DYNAMICS;
D O I
10.1016/j.brainresbull.2020.11.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An increasing number of studies connect neuronal activity with developmental myelination but how neuronal activity regulates remyelination has not been clarified. In this study, we induced the demyelination of the dorsal corticospinal tract (dCST) by a mild contusion spinal cord injury (SCI) on the T10 segment, and manipulated the neuronal activity of the primary motor cortex (M1) using chemogenetic viruses to induce activity and to suppress it. We found that oligodendrocyte precursor cell (OPC) proliferation and oligodendrocyte maturity following remyelination was strengthened after 4-week of neuronal activity stimulation. Furthermore, hindlimb motor function was also found to be improved. Vice versa, suppression of neuronal activity attenuated these effects. These results indicate that bidirectional regulation of neuronal activity can effectively modulate the development of oligodendrocyte lineage cells and the remyelination process. Neuronal activity supports the proliferation of OPCs, improves oligodendrocyte maturation and amplifies the axonal remyelination process, even though leads to better motor function recovery. Manipulation of neuronal activity in a non-invasive manner is therefore a promising avenue for exploration towards the treatment of central nervous system (CNS) demyelination diseases.
引用
收藏
页码:73 / 81
页数:9
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