Laboratory of Molecular Virology and Biotechnology, Institute of Biotechnology, National Cheng Kung University, Tainan, Taiwan.
PLoS One. 2011;6(8):e22935. doi: 10.1371/journal.pone.0022935. Epub 2011 Aug 25.
Aquatic birnavirus induces mitochondria-mediated cell death, but whether connects to endoplasmic reticulum (ER) stress is still unknown. In this present, we characterized that IPNV infection triggers ER stress-mediated cell death via PKR/eIF2α phosphorylation signaling for regulating the Bcl-2 family protein expression in fish cells. The IPNV infection can induce ER stress as follows: (1) ER stress sensor ATF6 cleavaged; (2) ER stress marker GRP78 upregulation, and (3) PERK/eIF2α phosphorylation. Then, the IPNV-induced ER stress signals can induce the CHOP expression at early (6 h p.i.) and middle replication (12 h p.i.) stages. Moreover, IPNV-induced CHOP upregulation dramatically correlates to apparently downregulate the Bcl-2 family proteins, Bcl-2, Mcl-1 and Bcl-xL at middle replication stage (12 h p.i.) and produces mitochondria membrane potential (MMP) loss and cell death. Furthermore, with GRP78 synthesis inhibitor momitoxin (VT) and PKR inhibitor 2-aminopurine (2-AP) treatment for blocking GRP78 expression and eIF2α phosphorylation, PKR/PERK may involve in eIF2α phosphorylation/CHOP upregulation pathway that enhances the downstream regulators Bcl-2 family proteins expression and increased cell survival. Taken together, our results suggest that IPNV infection activates PKR/PERK/eIF2α ER stress signals for regulating downstream molecules CHOP upregulation and Bcl-2 family downregulation that led to induce mitochondria-mediated cell death in fish cells, which may provide new insight into RNA virus pathogenesis and disease.
水生动物双RNA 病毒诱导线粒体介导的细胞死亡,但与内质网(ER)应激的关联尚不清楚。在本研究中,我们证实了 IPNV 感染通过 PKR/eIF2α 磷酸化信号触发 ER 应激介导的细胞死亡,从而调节鱼类细胞中 Bcl-2 家族蛋白的表达。IPNV 感染可诱导以下 ER 应激:(1)ER 应激传感器 ATF6 裂解;(2)GRP78 上调,(3)PERK/eIF2α 磷酸化。然后,IPNV 诱导的 ER 应激信号可以在早期(感染后 6 小时)和中期复制(感染后 12 小时)诱导 CHOP 的表达。此外,IPNV 诱导的 CHOP 上调与明显下调 Bcl-2 家族蛋白 Bcl-2、Mcl-1 和 Bcl-xL 密切相关,在中期复制阶段(感染后 12 小时)产生线粒体膜电位(MMP)损失和细胞死亡。此外,用 GRP78 合成抑制剂莫替莫星(VT)和 PKR 抑制剂 2-氨基嘌呤(2-AP)处理以阻断 GRP78 表达和 eIF2α 磷酸化,PKR/PERK 可能参与 eIF2α 磷酸化/CHOP 上调途径,增强下游调节因子 Bcl-2 家族蛋白的表达并增加细胞存活。总之,我们的结果表明,IPNV 感染激活 PKR/PERK/eIF2α ER 应激信号,调节下游分子 CHOP 的上调和 Bcl-2 家族的下调,导致鱼类细胞中线粒体介导的细胞死亡,这可能为 RNA 病毒发病机制和疾病提供新的见解。