Gao Xingchun, Mi Yajing, Guo Na, Hu Zhifang, Hu Fengrui, Liu Dou, Gao Lei, Gou Xingchun, Jin Weilin
Institute of Basic Medical Sciences and Shaanxi key Laboratory of ischemic Cardiovascular Disease, Xi'an Medical University, Xi'an 710021, P. R. China.
Institute of Nano Biomedicine and Engineering, Department of Instrument Science and Engineering, Key Lab. for Thin Film and Microfabrication Technology of Ministry of Education, School of Electronic Information and Electronic Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
Oncotarget. 2016 Dec 27;7(52):85963-85974. doi: 10.18632/oncotarget.13290.
Glioblastoma(GBM) is one of the most common and aggressive malignant primary tumors of the central nervous system and mitochondria have been proposed to participate in GBM tumorigenesis. Previous studies have identified a potential role of Disrupted in Schizophrenia 1 (DISC1), a multi-compartmentalized protein, in mitochondria. But whether DISC1 could regulate GBM tumorigenesis via mitochondria is still unknown. We determined the expression level of DISC1 by both bioinformatics analysis and tissue analysis, and found that DISC1 was highly expressed in GBM. Knocking down of DISC1 by shRNA in GBM cells significantly inhibited cell proliferation both in vitro and in vivo. In addition, down-regulation of DISC1 decreased cell migration and invasion of GBM and self renewal capacity of glioblastoma stem-like cells. Furthermore, multiple independent rings or spheres could be observed in mitochondria in GBM depleted of DISC1, while normal filamentous morphology was observed in control cells, demonstrating that DISC1 affected the mitochondrial dynamic. Dynamin-related protein 1 (Drp1) was reported to contribute to mitochondrial dynamic regulation and influence glioma cells proliferation and invasion by RHOA/ ROCK1 pathway. Our data showed a significant decrease of Drp1 both in mRNA and protein level in GBM lack of DISC1, indicating that DISC1 maybe affect the mitochondrial dynamic by regulating Drp1. Taken together, our findings reveal that DISC1 affects glioblastoma cell development via mitochondria dynamics partly by down regulation of Drp1.
胶质母细胞瘤(GBM)是中枢神经系统最常见且侵袭性最强的原发性恶性肿瘤之一,线粒体被认为参与了GBM的肿瘤发生过程。先前的研究已确定精神分裂症1号基因(DISC1)这一具有多区域化分布的蛋白质在线粒体中具有潜在作用。但DISC1是否能通过线粒体调节GBM的肿瘤发生仍不清楚。我们通过生物信息学分析和组织分析确定了DISC1的表达水平,发现DISC1在GBM中高表达。在GBM细胞中利用短发夹RNA(shRNA)敲低DISC1显著抑制了细胞在体外和体内的增殖。此外,DISC1的下调降低了GBM细胞的迁移、侵袭能力以及胶质母细胞瘤干细胞样细胞的自我更新能力。此外,在敲低DISC1的GBM细胞中,线粒体可观察到多个独立的环或球状体,而对照细胞中观察到正常的丝状形态,这表明DISC1影响了线粒体动力学。据报道,动力相关蛋白1(Drp1)有助于线粒体动力学调节,并通过RHOA/ROCK1途径影响胶质瘤细胞的增殖和侵袭。我们的数据显示,在缺乏DISC1的GBM中,Drp1的mRNA和蛋白水平均显著降低,表明DISC1可能通过调节Drp1影响线粒体动力学。综上所述,我们的研究结果表明,DISC1通过线粒体动力学部分地通过下调Drp1来影响胶质母细胞瘤细胞的发育。