Niu Xin, Brahmbhatt Hetal, Mergenthaler Philipp, Zhang Zhi, Sang Jing, Daude Michael, Ehlert Fabian G R, Diederich Wibke E, Wong Eve, Zhu Weijia, Pogmore Justin, Nandy Jyoti P, Satyanarayana Maragani, Jimmidi Ravi K, Arya Prabhat, Leber Brian, Lin Jialing, Culmsee Carsten, Yi Jing, Andrews David W
Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada; Department of Biochemistry and Molecular Cell Biology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada; Biological Sciences, Sunnybrook Research Institute, University of Toronto, Toronto, ON M4N 3M5, Canada.
Cell Chem Biol. 2017 Apr 20;24(4):493-506.e5. doi: 10.1016/j.chembiol.2017.03.011. Epub 2017 Apr 6.
Aberrant apoptosis can lead to acute or chronic degenerative diseases. Mitochondrial outer membrane permeabilization (MOMP) triggered by the oligomerization of the Bcl-2 family proteins Bax/Bak is an irreversible step leading to execution of apoptosis. Here, we describe the discovery of small-molecule inhibitors of Bax/Bak oligomerization that prevent MOMP. We demonstrate that these molecules disrupt multiple, but not all, interactions between Bax dimer interfaces thereby interfering with the formation of higher-order oligomers in the MOM, but not recruitment of Bax to the MOM. Small-molecule inhibition of Bax/Bak oligomerization allowed cells to evade apoptotic stimuli and rescued neurons from death after excitotoxicity, demonstrating that oligomerization of Bax is essential for MOMP. Our discovery of small-molecule Bax/Bak inhibitors provides novel tools for the investigation of the mechanisms leading to MOMP and will ultimately facilitate development of compounds inhibiting Bax/Bak in acute and chronic degenerative diseases.
异常凋亡可导致急性或慢性退行性疾病。由Bcl-2家族蛋白Bax/Bak寡聚化触发的线粒体外膜通透性改变(MOMP)是导致凋亡执行的不可逆步骤。在此,我们描述了阻止MOMP的Bax/Bak寡聚化小分子抑制剂的发现。我们证明这些分子破坏了Bax二聚体界面之间的多种(但不是全部)相互作用,从而干扰了线粒体外膜中高阶寡聚体的形成,但不影响Bax募集到线粒体外膜。对Bax/Bak寡聚化的小分子抑制使细胞能够逃避凋亡刺激,并在兴奋性毒性后挽救神经元免于死亡,这表明Bax的寡聚化对于MOMP至关重要。我们对小分子Bax/Bak抑制剂的发现为研究导致MOMP的机制提供了新工具,并最终将促进在急性和慢性退行性疾病中抑制Bax/Bak的化合物的开发。