Gu Wenbo, Zhang Xiao, Yuan Xiaoya, Cao Donghui, Zhao Hongyang, Hu Jinlong, Yuan Haifeng
Department of Spinal Surgery, General Hospital of Ningxia Medical University, Yinchuan 750001, Ningxia, China; The First Clinical Medical College, Ningxia Medical University, Yinchuan 750004, Ningxia, China.
University of Southern California, Bovard Administration Building, 3551 Trousdale Pkwy, Los Angeles, CA 90089, USA.
Biochim Biophys Acta Mol Basis Dis. 2025 Oct;1871(7):167929. doi: 10.1016/j.bbadis.2025.167929. Epub 2025 May 28.
To evaluate the therapeutic potential of NEP1-40-expressing neural stem cells (NSCs) in improving outcomes in spinal cord injury (SCI) by modulating the RhoA/ROCK signaling pathway. NEP1-40 was overexpressed by transfecting isolated NSCs with NEP1-40 lentivirus, and their differentiation following Nogo-A treatment was assessed via Tuj-1 immunofluorescence. The effects of NEP1-40 overexpression on axonal damage of differentiated NSCs and DRG neurons were examined using Tuj-1 and F-actin immunofluorescence, along with Western blotting for GAP-43, MAP-2, and APP. The activation of RhoA/ROCK and its downstream pathways, namely, PTEN/PI3K/AKT and MLC/LIMK, were analyzed by Western blotting. In a rat SCI model, following NSC transplantation, was assessed by examining neuronal regeneration markers. Furthermore, the Basso, Beattie, and Bresnahan (BBB) scale behavioral tests were used to assess motor function recovery. NEP1-40 overexpression inhibited the RhoA/ROCK signaling, followed by the stimulating the PI3K/AKT pathway and promoting neuronal differentiation under Nogo-A treatment. The inhibition of RhoA/ROCK signaling suppressed the MLC/LIMK pathway to enhance neurite outgrowth in NSC-differentiated and DRG neurons. In SCI rats, NEP1-40 overexpression increased the number of NSCs and neurons, whereas NEP1-40 overexpression in NSCs significantly increased the number of 5-HT-, ChAT-, and CGRP-positive neurons, as well as the levels of p-GAP-43, GAP-43 and MAP-2, and reduced the level of APP. These changes were accompanied by improved BBB scores. NEP1-40-modified NSCs enhance SCI recovery by activating the PI3K/AKT pathway and inhibiting the MLC/LIMK cascade, thereby promoting neuronal differentiation and reducing axonal damage. Altogether, this approach demonstrates promising therapeutic potential to improve NSC efficacy in SCI.
通过调节RhoA/ROCK信号通路,评估表达NEP1-40的神经干细胞(NSCs)在改善脊髓损伤(SCI)预后方面的治疗潜力。通过用NEP1-40慢病毒转染分离的神经干细胞来过表达NEP1-40,并通过Tuj-1免疫荧光评估其在Nogo-A处理后的分化情况。使用Tuj-1和F-肌动蛋白免疫荧光以及针对GAP-43、MAP-2和APP的蛋白质印迹法,检测NEP1-40过表达对分化的神经干细胞和背根神经节(DRG)神经元轴突损伤的影响。通过蛋白质印迹法分析RhoA/ROCK及其下游通路(即PTEN/PI3K/AKT和MLC/LIMK) 的激活情况。在大鼠脊髓损伤模型中,通过检测神经元再生标志物来评估神经干细胞移植后的情况。此外,使用Basso、Beattie和Bresnahan(BBB)行为评分量表来评估运动功能恢复情况。NEP1-40过表达抑制RhoA/ROCK信号,随后刺激PI3K/AKT通路并促进Nogo-A处理下的神经元分化。RhoA/ROCK信号的抑制抑制了MLC/LIMK通路,以增强神经干细胞分化的神经元和背根神经节神经元的神经突生长。在脊髓损伤大鼠中,NEP1-40过表达增加了神经干细胞和神经元的数量,而神经干细胞中NEP1-40过表达显著增加了5-羟色胺、胆碱乙酰转移酶和降钙素基因相关肽阳性神经元的数量,以及p-GAP-43、GAP-43和MAP-2的水平,并降低了APP的水平。这些变化伴随着BBB评分的改善。NEP1-40修饰的神经干细胞通过激活PI3K/AKT通路和抑制MLC/LIMK级联反应来增强脊髓损伤的恢复,从而促进神经元分化并减少轴突损伤。总之,这种方法显示出改善神经干细胞在脊髓损伤中疗效的有前景的治疗潜力。