Xu Xiang, Huang Enping, Luo Baoying, Cai Dunpeng, Zhao Xu, Luo Qin, Jin Yili, Chen Ling, Wang Qi, Liu Chao, Lin Zhoumeng, Xie Wei-Bing, Wang Huijun
School of Forensic Medicine, Southern Medical University, Guangzhou, China.
School of Forensic Medicine, Wannan Medical College, Wuhu, China.
FASEB J. 2018 Jun 25:fj201701460RRR. doi: 10.1096/fj.201701460RRR.
Methamphetamine (Meth) is a widely abused psychoactive drug that primarily damages the nervous system, notably causing dopaminergic neuronal apoptosis. CCAAT-enhancer binding protein (C/EBPβ) is a transcription factor and an important regulator of cell apoptosis and autophagy. Insulin-like growth factor binding protein (IGFBP5) is a proapoptotic factor that mediates Meth-induced neuronal apoptosis, and Trib3 (tribbles pseudokinase 3) is an endoplasmic reticulum (ER) stress-inducible gene involved in autophagic cell death through the mammalian target of rapamycin (mTOR) signaling pathway. To test the hypothesis that C/EBPβ is involved in Meth-induced IGFBP5-mediated neuronal apoptosis and Trib3-mediated neuronal autophagy, we measured the protein expression of C/EBPβ after Meth exposure and evaluated the effects of silencing C/EBPβ, IGFBP5, or Trib3 on Meth-induced apoptosis and autophagy in neuronal cells and in the rat striatum after intrastriatal Meth injection. We found that, at relatively high doses, Meth exposure increased C/EBPβ protein expression, which was accompanied by increased neuronal apoptosis and autophagy; triggered the IGFBP5-mediated, p53-up-regulated modulator of apoptosis (PUMA)-related mitochondrial apoptotic signaling pathway; and stimulated the Trib3-mediated ER stress signaling pathway through the Akt-mTOR signaling axis. We also found that autophagy is an early response to Meth-induced stress upstream of apoptosis and plays a detrimental role in Meth-induced neuronal cell death. These results suggest that Meth exposure induces C/EBPβ expression, which plays an essential role in the neuronal apoptosis and autophagy induced by relatively high doses of Meth; however, relatively low concentrations of Meth did not change the expression of C/EBPβ in vitro. Further studies are needed to elucidate the role of C/EBPβ in low-dose Meth-induced neurotoxicity.-Xu, X., Huang, E., Luo, B., Cai, D., Zhao, X., Luo, Q., Jin, Y., Chen, L., Wang, Q., Liu, C., Lin, Z., Xie, W.-B., Wang, H. Methamphetamine exposure triggers apoptosis and autophagy in neuronal cells by activating the C/EBPβ-related signaling pathway.
甲基苯丙胺(冰毒)是一种广泛滥用的精神活性药物,主要损害神经系统,尤其会导致多巴胺能神经元凋亡。CCAAT增强子结合蛋白(C/EBPβ)是一种转录因子,是细胞凋亡和自噬的重要调节因子。胰岛素样生长因子结合蛋白(IGFBP5)是一种促凋亡因子,介导冰毒诱导的神经元凋亡,而TRIB3(TRIBBLES假激酶3)是一种内质网(ER)应激诱导基因,通过雷帕霉素靶蛋白(mTOR)信号通路参与自噬性细胞死亡。为了验证C/EBPβ参与冰毒诱导的IGFBP5介导的神经元凋亡和TRIB3介导的神经元自噬这一假说,我们检测了冰毒暴露后C/EBPβ的蛋白表达,并评估了沉默C/EBPβ、IGFBP5或TRIB3对神经元细胞以及纹状体内注射冰毒后大鼠纹状体中冰毒诱导的凋亡和自噬的影响。我们发现,在相对高剂量下,冰毒暴露会增加C/EBPβ蛋白表达,同时伴有神经元凋亡和自噬增加;触发IGFBP5介导的、p53上调凋亡调节因子(PUMA)相关的线粒体凋亡信号通路;并通过Akt-mTOR信号轴刺激TRIB3介导的内质网应激信号通路。我们还发现自噬是冰毒诱导的应激在凋亡上游的早期反应,并且在冰毒诱导的神经元细胞死亡中起有害作用。这些结果表明,冰毒暴露会诱导C/EBPβ表达,其在相对高剂量冰毒诱导的神经元凋亡和自噬中起重要作用;然而,相对低浓度的冰毒在体外并未改变C/EBPβ的表达。需要进一步研究来阐明C/EBPβ在低剂量冰毒诱导的神经毒性中的作用。-徐,X.,黄,E.,罗,B.,蔡,D.,赵,X.,罗,Q.,金,Y.,陈,L.,王,Q.,刘,C.,林,Z.,谢,W.-B.,王,H. 甲基苯丙胺暴露通过激活C/EBPβ相关信号通路触发神经元细胞凋亡和自噬