Wohlfromm Fabian, Richter Max, Otrin Lado, Seyrek Kamil, Vidaković-Koch Tanja, Kuligina Elena, Richter Vladimir, Koval Olga, Lavrik Inna N
Translational Inflammation Research, Medical Faculty, Otto von Guericke University, Magdeburg, Germany.
Max Planck Institute for Dynamics of Complex Technical Systems, Magdeburg, Germany.
Front Cell Dev Biol. 2021 Jan 18;8:617762. doi: 10.3389/fcell.2020.617762. eCollection 2020.
A recombinant fragment of human κ-Casein, termed RL2, induces cell death of breast cancer cells; however, molecular mechanisms of RL2-mediated cell death have remained largely unknown. In the current study, we have decoded the molecular mechanism of the RL2-mediated cell death and found that RL2 acts via the induction of mitophagy. This was monitored by the loss of adenosine triphosphate production, LC3B-II generation, and upregulation of BNIP3 and BNIP3L/NIX, as well as phosphatase and tensin homolog-induced kinase 1. Moreover, we have analyzed the cross talk of this pathway with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis upon combinatorial treatment with RL2 and TRAIL. Strikingly, we found two opposite effects of this co-treatment. RL2 had inhibitory effects on TRAIL-induced cell death upon short-term co-stimulation. In particular, RL2 treatment blocked TRAIL-mediated caspase activation, cell viability loss, and apoptosis, which was mediated via the downregulation of the core proapoptotic regulators. Contrary to short-term co-treatment, upon long-term co-stimulation, RL2 sensitized the cells toward TRAIL-induced cell death; the latter observation provides the basis for the development of therapeutic approaches in breast cancer cells. Collectively, our findings have important implications for cancer therapy and reveal the molecular switches of the cross talk between RL2-induced mitophagy and TRAIL-mediated apoptosis.
一种名为RL2的人κ-酪蛋白重组片段可诱导乳腺癌细胞死亡;然而,RL2介导的细胞死亡的分子机制在很大程度上仍不清楚。在当前的研究中,我们已经解析了RL2介导的细胞死亡的分子机制,并发现RL2通过诱导线粒体自噬发挥作用。这通过三磷酸腺苷产生的丧失、LC3B-II的生成、BNIP3和BNIP3L/NIX的上调以及磷酸酶和张力蛋白同源物诱导激酶1来监测。此外,我们分析了该途径与肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的凋亡在与RL2和TRAIL联合处理时的相互作用。令人惊讶的是,我们发现这种联合处理有两种相反的效果。在短期共刺激时,RL2对TRAIL诱导的细胞死亡有抑制作用。特别是,RL2处理阻断了TRAIL介导的半胱天冬酶激活、细胞活力丧失和凋亡,这是通过核心促凋亡调节因子的下调介导的。与短期联合处理相反,在长期共刺激时,RL2使细胞对TRAIL诱导的细胞死亡敏感;后一观察结果为乳腺癌细胞治疗方法的开发提供了基础。总的来说,我们的发现对癌症治疗具有重要意义,并揭示了RL2诱导的线粒体自噬和TRAIL介导的凋亡之间相互作用的分子开关。