Department of Orthopedics, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, 200072, China.
Spinal Pain Research Institute, Tongji University School of Medicine, Shanghai, 200072, China.
Neurosci Bull. 2020 Apr;36(4):372-384. doi: 10.1007/s12264-019-00442-0. Epub 2019 Nov 16.
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.
硬膜外脊髓电刺激(ESCS)显著改善脊髓损伤(SCI)后的运动和感觉功能,但潜在机制尚不清楚。在这里,我们研究了 ESCS 是否会影响 SCI 大鼠的少突胶质细胞分化及其细胞和分子机制。ESCS 可改善 SCI 后 7 天、14 天、21 天和 28 天的后肢运动功能。ESCS 还可显著增加 28 天时的髓鞘面积,并减少 7 天时脊髓白质中的凋亡细胞数量。SCI 可降低 7 天时 2',3'-环核苷酸 3'-磷酸二酯酶(CNPase,少突胶质细胞标志物)的表达和 28 天时髓鞘碱性蛋白的表达。ESCS 可显著上调这些标志物,并增加 Sox2/CNPase/DAPI 阳性细胞(新分化的少突胶质细胞)的百分比在 7 天时。重组人骨形态发生蛋白 4(rhBMP4)在 ESCS 后明显下调了这些因子。此外,ESCS 可显著降低 SCI 后 BMP4 和 p-Smad1/5/9 的表达,而 rhBMP4 则降低了 ESCS 的这种作用。这些发现表明,ESCS 通过抑制 BMP4-Smad1/5/9 信号通路,增强少突胶质细胞的存活和分化,保护髓鞘,并促进运动功能恢复。