Zou Cheng-Gang, Cao Xiu-Zhen, Zhao Yue-Shui, Gao Shun-Yu, Li Shu-De, Liu Xian-Yong, Zhang Yan, Zhang Ke-Qin
Laboratory for Conservation and Utilization of Bio-Resources, Yunnan University, Kunming, Yunnan 650091, China.
Endocrinology. 2009 Jan;150(1):277-85. doi: 10.1210/en.2008-0794. Epub 2008 Sep 18.
Endoplasmic reticulum (ER) stress has been implicated in several neurodegenerative diseases. Although CCAAT/enhancer-binding protein homologous protein (CHOP) has been shown to play a critical role in ER stress, the precise apoptosis cascade downstream of CHOP is unknown. In this report, we investigated the mechanism of ER stress-mediated apoptosis as well as the action of IGF-I in PC-12 neuronal cells. Our results demonstrated that tribbles-related protein 3 (TRB3), which is a target gene of CHOP, was responsible for tunicamycin (an ER stress inducer)-induced apoptosis. TRB3 could promote dephosphorylation of Akt in PC-12 cells. IGF-I inhibited ER stress-induced apoptosis by restoring the phosphorylation level of Akt. Both wortmannin (a phosphatidylinositide 3-kinase inhibitor) and SB 212090 (a p38 MAPK inhibitor) suppressed the protective effect of IGF-I on ER stress-induced apoptosis. Interestingly, IGF-I attenuated ER stress-mediated expression of TRB3 but not CHOP. This action of IGF-I was abolished by SB 212090 but not by wortmannin. Immunoprecipitation analysis revealed that IGF-I promoted the phosphorylation of CHOP by activating p38 MAPK, probably leading to a decrease in the transcriptional activity of CHOP. The dephosphorylation of Akt resulted in increased expression of a proapoptotic protein, p53 up-regulated modulator of apoptosis (PUMA), in a forkhead box O3a-dependent manner. Knockdown of PUMA by short hairpin RNA attenuated ER stress-mediated apoptosis. Thus, our current study indicates that both TRB3 and PUMA are critical molecules in ER stress-induced apoptosis. IGF-I effectively protects PC-12 neuronal cells against ER stress-induced apoptosis through the phosphatidylinositide 3-kinase/Akt and p38 MAPK pathways.
内质网(ER)应激与多种神经退行性疾病有关。尽管CCAAT/增强子结合蛋白同源蛋白(CHOP)已被证明在ER应激中起关键作用,但CHOP下游精确的凋亡级联反应尚不清楚。在本报告中,我们研究了ER应激介导的凋亡机制以及胰岛素样生长因子-I(IGF-I)在PC-12神经元细胞中的作用。我们的结果表明,作为CHOP靶基因的TRIB3相关蛋白3(TRB3),介导了衣霉素(一种ER应激诱导剂)诱导的凋亡。TRB3可促进PC-12细胞中Akt的去磷酸化。IGF-I通过恢复Akt的磷酸化水平抑制ER应激诱导的凋亡。渥曼青霉素(一种磷脂酰肌醇3激酶抑制剂)和SB 212090(一种p38丝裂原活化蛋白激酶抑制剂)均抑制了IGF-I对ER应激诱导凋亡的保护作用。有趣的是,IGF-I减弱了ER应激介导的TRB3表达,但不影响CHOP的表达。IGF-I的这种作用被SB 212090消除,但未被渥曼青霉素消除。免疫沉淀分析显示,IGF-I通过激活p38丝裂原活化蛋白激酶促进CHOP的磷酸化,这可能导致CHOP转录活性降低。Akt的去磷酸化导致促凋亡蛋白p53上调凋亡调节因子(PUMA)的表达增加,且呈叉头框O3a依赖性。通过短发夹RNA敲低PUMA可减弱ER应激介导的凋亡。因此,我们目前的研究表明,TRB3和PUMA都是ER应激诱导凋亡的关键分子。IGF-I通过磷脂酰肌醇3激酶/Akt和p38丝裂原活化蛋白激酶途径有效保护PC-12神经元细胞免受ER应激诱导的凋亡。