Epidural Spinal Cord Stimulation Promotes Motor Functional Recovery by Enhancing Oligodendrocyte Survival and Differentiation and by Protecting Myelin after Spinal Cord Injury in Rats

被引:0
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作者
Gang Li
Zhong-Kai Fan
Guang-Fei Gu
Zhi-Qiang Jia
Qiang-Qiang Zhang
Jun-Yu Dai
Shi-Sheng He
机构
[1] Tongji University School of Medicine,Department of Orthopedics, Shanghai Tenth People’s Hospital
[2] Tongji University School of Medicine,Spinal Pain Research Institute
[3] Jinzhou Medical University,Department of Orthopaedics, The First Affiliated Hospital
[4] Henan University of Science and Technology,Department of Spinal Surgery, The Second Affiliated Hospital
来源
Neuroscience Bulletin | 2020年 / 36卷
关键词
Spinal cord injury; Epidural spinal cord stimulation; Oligodendrocyte; Differentiation; Remyelination;
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摘要
Epidural spinal cord stimulation (ESCS) markedly improves motor and sensory function after spinal cord injury (SCI), but the underlying mechanisms are unclear. Here, we investigated whether ESCS affects oligodendrocyte differentiation and its cellular and molecular mechanisms in rats with SCI. ESCS improved hindlimb motor function at 7 days, 14 days, 21 days, and 28 days after SCI. ESCS also significantly increased the myelinated area at 28 days, and reduced the number of apoptotic cells in the spinal white matter at 7 days. SCI decreased the expression of 2′,3′-cyclic-nucleotide 3′-phosphodiesterase (CNPase, an oligodendrocyte marker) at 7 days and that of myelin basic protein at 28 days. ESCS significantly upregulated these markers and increased the percentage of Sox2/CNPase/DAPI-positive cells (newly differentiated oligodendrocytes) at 7 days. Recombinant human bone morphogenetic protein 4 (rhBMP4) markedly downregulated these factors after ESCS. Furthermore, ESCS significantly decreased BMP4 and p-Smad1/5/9 expression after SCI, and rhBMP4 reduced this effect of ESCS. These findings indicate that ESCS enhances the survival and differentiation of oligodendrocytes, protects myelin, and promotes motor functional recovery by inhibiting the BMP4-Smad1/5/9 signaling pathway after SCI.
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页码:372 / 384
页数:12
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