Hu Zhenxin, Wu Tingting, Zhou Ziheng, Zhang Yu, Chen Qiyue, Yao Hanbing, Ji Mengchu, Shen Ge, Dong Chenling, Shi Chengge, Huang Zhixian, Jiang Nizhou, Han Nan, Tian Xiliang
Department of Orthopedics, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
The First Clinical Medical College, Wenzhou Medical University, Wenzhou, 325035, China.
Mol Neurobiol. 2024 Feb;61(2):678-692. doi: 10.1007/s12035-023-03605-3. Epub 2023 Sep 1.
The blood-spinal cord barrier (BSCB) plays a vital role in the recovery of spinal cord function after spinal cord injury (SCI). Pericytes, pluripotent members of the neurovascular unit (NVU), receive signals from neighboring cells and are critical for maintaining CNS function. Therapeutic targets for the BSCB include endothelial cells (ECs) and glial cells, but few drugs target pericytes. This study was designed to explore whether asiaticoside has a positively effect on pericytes and the integrity of the BSCB. In this study, we found that asiaticoside could inhibit the loss of junction proteins just 1 day after SCI in vivo, but our in vitro study showed no significant differences in the expression of endothelial junction proteins between the control and asiaticoside treatment groups. We also found that asiaticoside could inhibit endoplasmic reticulum (ER) stress and pericyte apoptosis, which might be associated with the inhibition of junction protein reduction in ECs. Thus, we investigated the interactions between pericytes and ECs. Our results showed that asiaticoside could decrease the release of matrix metalloproteinase (MMP)-9 in pericytes and therefore upregulate the expression of junction proteins in ECs. Furthermore, the protective effect of asiaticoside on pericytes is related to the inhibition of ER stress via the MAPK signaling pathway. Taken together, our results demonstrate that asiaticoside treatment inhibits BSCB disruption and enhances functional recovery after SCI.
血脊髓屏障(BSCB)在脊髓损伤(SCI)后脊髓功能的恢复中起着至关重要的作用。周细胞是神经血管单元(NVU)的多能成员,接收来自相邻细胞的信号,对维持中枢神经系统功能至关重要。血脊髓屏障的治疗靶点包括内皮细胞(ECs)和神经胶质细胞,但很少有药物作用于周细胞。本研究旨在探讨积雪草苷是否对周细胞和血脊髓屏障的完整性有积极作用。在本研究中,我们发现积雪草苷在体内脊髓损伤后仅1天就能抑制连接蛋白的丢失,但我们的体外研究表明,对照组和积雪草苷治疗组之间内皮连接蛋白的表达没有显著差异。我们还发现积雪草苷可以抑制内质网(ER)应激和周细胞凋亡,这可能与抑制内皮细胞连接蛋白减少有关。因此,我们研究了周细胞与内皮细胞之间的相互作用。我们的结果表明,积雪草苷可以减少周细胞中基质金属蛋白酶(MMP)-9的释放,从而上调内皮细胞中连接蛋白的表达。此外,积雪草苷对周细胞的保护作用与通过丝裂原活化蛋白激酶(MAPK)信号通路抑制内质网应激有关。综上所述,我们的结果表明,积雪草苷治疗可抑制血脊髓屏障破坏,并促进脊髓损伤后的功能恢复。