Department of Neurology, Second Xiangya Hospital, Central South University, Changsha, China.
J Cell Physiol. 2018 Sep;233(9):7480-7496. doi: 10.1002/jcp.26602. Epub 2018 Apr 16.
Cerebral ischemia/reperfusion-induced injury plays a significant role in the development of multi-subcellular organelles injury after ischemic stroke. UBIAD1 was discovered originally as a potential tumor suppressor protein. Recently, analysis of UBIAD1 has indicated it is a prenyltransferase enzyme for both non-mitochondrial CoQ10 and vitamin K2 production. Further, UBIAD1 has been localized to multiple subcellular organelles. Particularly, UBIAD1 plays an important role in the regulation of oxidative stress, apoptosis and cell proliferation, cholesterol and lipid metabolism, which was closely associated with the cerebral ischemic/reperfusion mechanism. However, the mechanism underlying effects of UBIAD1 on cerebral ischemia/reperfusion-induced injury remains largely unknown. We aimed to investigate the effects of UBIAD1 on ischemia/reperfusion-induced multiple subcellular organelles injury in vitro, mouse N2A cells were subjected to a classical oxygen-glucose deprivation and reperfusion (OGD/R) insult. The expression of UBIAD1 was reduced in mouse N2A cells after OGD/R. UBIAD1 exhibits multi-subcellular organelles co-localization in N2a cells, including in the mitochondria, endoplasmic reticulum, and Golgi apparatus. The over-expression of UBIAD1 significantly protects against OGD/R-induced cell death. UBIAD1 over-expression also attenuated OGD/R-induced mitochondrial fragmentation and dysfunction and mediated the level of apoptosis-associated protein. Moreover, we observed that the over-expression of UBIAD1 ameliorated OGD/R-induced fragmentation and reduced the level of oxidative stress-related protein expression in both the endoplasmic reticulum and Golgi apparatus. Besides, the neuroprotective effect of UBIAD1 was correlated with the PI3K/AKT pathway, which was demonstrated using the PI3K inhibitor LY294002 and perifosion. Collectively, these findings identified that UBIAD1 protects against OGD/R-induced multiple subcellular organelles injury through PI3K/AKT Pathway.
脑缺血/再灌注诱导损伤在缺血性脑卒中后多细胞器官损伤的发展中起重要作用。UBIAD1 最初被发现是一种潜在的肿瘤抑制蛋白。最近,对 UBIAD1 的分析表明,它是一种非线粒体 CoQ10 和维生素 K2 产生的 prenyltransferase 酶。此外,UBIAD1 已定位于多种亚细胞细胞器。特别是,UBIAD1 在调节氧化应激、细胞凋亡和细胞增殖、胆固醇和脂质代谢方面发挥着重要作用,这与脑缺血/再灌注机制密切相关。然而,UBIAD1 对脑缺血/再灌注诱导损伤的影响的机制在很大程度上仍然未知。我们旨在研究 UBIAD1 对体外缺血/再灌注诱导的多细胞器官损伤的影响,将小鼠 N2A 细胞置于经典的氧葡萄糖剥夺和再灌注(OGD/R)损伤中。OGD/R 后,小鼠 N2A 细胞中的 UBIAD1 表达减少。UBIAD1 在 N2a 细胞中表现出多细胞器官共定位,包括线粒体、内质网和高尔基体。UBIAD1 的过表达显著防止 OGD/R 诱导的细胞死亡。UBIAD1 的过表达还减弱了 OGD/R 诱导的线粒体片段化和功能障碍,并调节了凋亡相关蛋白的水平。此外,我们观察到 UBIAD1 的过表达改善了 OGD/R 诱导的片段化并降低了内质网和高尔基体中氧化应激相关蛋白表达的水平。此外,UBIAD1 的神经保护作用与 PI3K/AKT 通路相关,这是通过使用 PI3K 抑制剂 LY294002 和渗透实验来证明的。总之,这些发现表明,UBIAD1 通过 PI3K/AKT 通路保护 OGD/R 诱导的多细胞器官损伤。