Department of Neurosurgery, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Neurosurgery, People's Hospital of Chiping City, Liaocheng City, Shandong Province, China.
J Mol Neurosci. 2020 Nov;70(11):1728-1741. doi: 10.1007/s12031-020-01566-z. Epub 2020 Jun 3.
Secreted protein acidic and rich in cysteine (SPARC) has a close association with inflammatory response and oxidative stress in tissues and is widely expressed in intracranial aneurysms (IAs), especially in smooth muscle cells. Therefore, it is inferred that SPARC might be involved in the formation and development of IAs through the inflammatory response pathway or oxidative stress pathway. The aim of this study is to investigate the pathological mechanism of SPARC in oxidative stress, inflammation, and apoptosis during the formation of IAs, as well as the involvement of TGF-β1 and NOX4 molecules. Human brain vascular smooth muscle cells (HBVSMCs) were selected as experimental objects. After the cells were stimulated by recombinant human SPARC protein in vitro, the ROS level in the cells was measured using an ID/ROS fluorescence analysis kit combined with fluorescence microscope and flow cytometry. The related protein expression in HBVSMCs was measured using western blotting. The mitochondrial membrane potential change was detected using a mitochondrial membrane potential kit and laser confocal microscope. The mechanism was explored by intervention with reactive oxygen scavengers N-acetylcysteine (NAC), TGF-β1 inhibitor (SD-208), and siRNA knockout. The results showed that SPARC upregulated the expression of NOX4 through the TGF-β1-dependent signaling pathway, leading to oxidative stress and pro-inflammatory matrix behavior and apoptosis in HBVSMCs. These findings demonstrated that SPARC may promote the progression of IAs.
富含半胱氨酸的酸性分泌蛋白(SPARC)与组织中的炎症反应和氧化应激密切相关,在颅内动脉瘤(IA)中广泛表达,尤其是在平滑肌细胞中。因此,推测 SPARC 可能通过炎症反应途径或氧化应激途径参与 IA 的形成和发展。本研究旨在探讨 SPARC 在 IA 形成过程中氧化应激、炎症和细胞凋亡中的病理机制,以及 TGF-β1 和 NOX4 分子的参与。选择人脑血管平滑肌细胞(HBVSMCs)作为实验对象。体外用重组人 SPARC 蛋白刺激细胞后,采用 ID/ROS 荧光分析试剂盒结合荧光显微镜和流式细胞术检测细胞内 ROS 水平。采用 Western blot 检测 HBVSMCs 中的相关蛋白表达。采用线粒体膜电位试剂盒和激光共聚焦显微镜检测线粒体膜电位变化。通过活性氧清除剂 N-乙酰半胱氨酸(NAC)、TGF-β1 抑制剂(SD-208)和 siRNA 敲除进行干预,探讨其作用机制。结果表明,SPARC 通过 TGF-β1 依赖性信号通路上调 NOX4 的表达,导致 HBVSMCs 发生氧化应激、促炎基质行为和细胞凋亡。这些发现表明 SPARC 可能促进了 IA 的进展。