Institute for Experimental Cancer Research in Pediatrics, Goethe-University Frankfurt, Komturstrasse 3a, 60528, Frankfurt, Germany.
Glycoscience Group, National University of Ireland, Galway, Ireland.
Cell Death Dis. 2019 Feb 15;10(3):155. doi: 10.1038/s41419-019-1381-z.
Since Inhibitor of Apoptosis (IAP) proteins have been implicated in cellular adaptation to endoplasmic reticulum (ER) stress, we investigated the regulation of ER stress-induced apoptosis by small-molecule second mitochondria-derived activator of caspase (Smac) mimetics that antagonize IAP proteins. Here, we discover that Smac mimetic suppresses tunicamycin (TM)-induced apoptosis via resolution of the unfolded protein response (UPR) and ER stress. Smac mimetics such as BV6 selectively inhibit apoptosis triggered by pharmacological or genetic inhibition of protein N-glycosylation using TM or knockdown of DPAGT1, the enzyme that catalyzes the first step of protein N-glycosylation. In contrast, BV6 does not rescue cell death induced by other typical ER stressors (i.e., thapsigargin (TG), dithiothreitol, brefeldin A, bortezomib, or 2-deoxyglucose). The protection from TM-triggered apoptosis is found for structurally different Smac mimetics and for genetic knockdown of cellular IAP (cIAP) proteins in several cancer types, underlining the broader relevance. Interestingly, lectin microarray profiling reveals that BV6 counteracts TM-imposed inhibition of protein glycosylation. BV6 consistently abolishes TM-stimulated accumulation of ER stress markers such as glucose-regulated protein 78 (GRP78) and C/EBP homologous protein (CHOP) and reduces protein kinase RNA-like ER kinase (PERK) phosphorylation and X box-binding protein 1 (XBP1) splicing upon TM treatment. BV6-stimulated activation of nuclear factor-κB (NF-κB) contributes to the resolution of ER stress, since NF-κB inhibition by overexpression of dominant-negative IκBα superrepressor counteracts the suppression of TM-stimulated transcriptional activation of CHOP and GRP78 by BV6. Thus, our study is the first to show that Smac mimetic protects from TM-triggered apoptosis by resolving the UPR and ER stress. This provides new insights into the regulation of cellular stress responses by Smac mimetics.
由于凋亡抑制蛋白(IAP)在细胞适应内质网(ER)应激方面发挥作用,我们研究了小分子第二线粒体衍生的半胱天冬酶激活剂(Smac)模拟物对 ER 应激诱导的细胞凋亡的调节,这些模拟物拮抗 IAP 蛋白。在这里,我们发现 Smac 模拟物通过解决未折叠蛋白反应(UPR)和 ER 应激来抑制他莫昔芬(TM)诱导的细胞凋亡。Smac 模拟物如 BV6 通过 TM 或 DPAGT1(催化蛋白 N-糖基化第一步的酶)的敲低来抑制药理学或遗传学抑制蛋白 N-糖基化所引发的细胞凋亡。相比之下,BV6 不能挽救其他典型 ER 应激物(即他普西龙(TG)、二硫苏糖醇、布雷菲德菌素 A、硼替佐米或 2-脱氧葡萄糖)诱导的细胞死亡。在几种癌症类型中,我们发现,对于结构不同的 Smac 模拟物以及细胞 IAP(cIAP)蛋白的基因敲低,TM 触发的细胞凋亡得到保护,这强调了更广泛的相关性。有趣的是,凝集素微阵列分析表明,BV6 对抗 TM 引起的蛋白糖基化抑制。BV6 一致消除 TM 刺激的 ER 应激标志物(如葡萄糖调节蛋白 78(GRP78)和 C/EBP 同源蛋白(CHOP))的积累,并减少蛋白激酶 RNA 样内质网激酶(PERK)磷酸化和 X 框结合蛋白 1(XBP1)剪接 TM 处理后。BV6 刺激的核因子-κB(NF-κB)的激活有助于缓解 ER 应激,因为过表达显性负性 IκBα 超阻遏物抑制 NF-κB 抑制 BV6 对 TM 刺激的 CHOP 和 GRP78 转录激活的抑制作用。因此,我们的研究首次表明,Smac 模拟物通过解决 UPR 和 ER 应激来保护 TM 触发的细胞凋亡。这为 Smac 模拟物对细胞应激反应的调节提供了新的见解。