Open Laboratory for Tumor Molecular Biology/Department of Biochemistry/The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Xinling Road 22, Shantou, China.
Cheung Kong Scholar Laboratory, Shantou University Medical College, Xinling Road 22, Shantou, China.
BMC Cancer. 2018 May 22;18(1):581. doi: 10.1186/s12885-018-4504-5.
All known mechanisms of apoptosis induced by resveratrol act through cell cycle arrest and changes in mitochondrial membrane potential. It is currently unknown whether resveratrol-induced apoptosis is associated with other physiological processes, such as autophagy.
Apoptosis-related markers involved in the intrinsic and extrinsic apoptotic pathways, and autophagic markers were detected by using western blotting and immunofluorescence. Mitochondrial membrane potential was assayed by flow cytometry. Pharmaceutical or genetic inhibition of autophagy involved were carried by 3- methyladenine or knockdown of autophagy-related (Atg) genes by siRNA. Differences between two values were tested by Student's unpaired t test.
We show that resveratrol-induced apoptosis occurs through both the intrinsic and extrinsic apoptotic pathways. Mitochondrial membrane potential and apoptosis-related markers, such as an increased Bax/Bcl-2 ratio, and cleaved forms of caspase-8 and caspase-3, arise following resveratrol addition. Moreover, we find that resveratrol increases both the levels of microtubule-associated protein 1 light chain 3-II and the number of autophagosomes, and further demonstrate that resveratrol-induced autophagy depends on the LKB1-AMPK-mTOR pathway. We next reveal that some apoptosis-related markers induced by resveratrol are further attenuated by the inhibition of autophagy with 3-methyladenine or knockdown of autophagy-related (Atg) genes by siRNA.
These results suggest that resveratrol induced apoptotic cell death of HL-60 cells depends on the autophagy activated through both the LKB1-AMPK and PI3K/AKT-regulated mTOR signaling pathways.
白藜芦醇诱导细胞凋亡的所有已知机制均通过细胞周期阻滞和线粒体膜电位变化起作用。目前尚不清楚白藜芦醇诱导的细胞凋亡是否与其他生理过程(如自噬)有关。
通过 Western blot 和免疫荧光检测凋亡相关的内源性和外源性凋亡途径的标志物和自噬标志物。通过流式细胞术检测线粒体膜电位。通过 3-甲基腺嘌呤或 siRNA 敲低自噬相关(Atg)基因抑制自噬。用 Student's unpaired t 检验测试两个值之间的差异。
我们表明白藜芦醇诱导的细胞凋亡通过内源性和外源性凋亡途径发生。线粒体膜电位和凋亡相关标志物(如 Bax/Bcl-2 比值增加,以及 caspase-8 和 caspase-3 的裂解形式)在白藜芦醇添加后出现。此外,我们发现白藜芦醇增加微管相关蛋白 1 轻链 3-II 的水平和自噬体的数量,并进一步表明白藜芦醇诱导的自噬依赖于 LKB1-AMPK-mTOR 途径。我们接下来揭示,一些白藜芦醇诱导的凋亡相关标志物通过 3-甲基腺嘌呤或 siRNA 敲低自噬相关(Atg)基因的抑制而进一步减弱。
这些结果表明,白藜芦醇诱导 HL-60 细胞的凋亡性细胞死亡依赖于通过 LKB1-AMPK 和 PI3K/AKT 调节的 mTOR 信号通路激活的自噬。