Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, PR China; Department of Medical Technology, Suzhou Vocational Health College, Suzhou, 215009, PR China.
Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, PR China; College of Life Sciences, Anhui Medical University, Anhui, 230032, PR China.
Neuropharmacology. 2022 Nov 15;219:109236. doi: 10.1016/j.neuropharm.2022.109236. Epub 2022 Aug 29.
Resveratrol is a natural polyphenol with neuroprotective function. The underlying mechanism is not well understood. Our previous studies have identified that resveratrol antagonizes cadmium (Cd) neurotoxicity via targeting PP2A/PP5-mediated Erk1/2 and JNK pathways. Here we show that resveratrol protected against Cd-poisoning also by blocking Cd-induced activation of mTORC1 and mTORC2 pathways in PC12 cells and murine primary neurons. Co-treatment with inhibitors of mTORC1 (rapamycin), mTORC1/2 (PP242), Erk1/2 (U0126) and/or JNK (SP600125), knockdown of mTOR, or disruption of mTORC1 and/or mTORC2 by silencing raptor, rictor or raptor/rictor, respectively, markedly potentiated the inhibitory effects of resveratrol on Cd-induced phosphorylation of S6K1/4E-BP1 (mTORC1 substrates), Akt (mTORC2 substrate), Erk1/2 and/or JNK/c-Jun, cleavage of caspase-3 and cell death in PC12 cells and/or primary neurons. Knockdown of S6K1 or 4E-BP1, or ectopic expression of constitutively hypophosphorylated 4E-BP1 (4E-BP1-5A) reinforced the resveratrol's inhibition on Cd-evoked cell death, whereas ectopic expression of constitutively active S6K1 or knockdown of 4E-BP1 attenuated the resveratrol's inhibition on Cd-induced cell death. Co-treatment with Akt inhibitor or overexpression of dominant negative Akt (dn-Akt) strengthened the resveratrol's suppression on Cd-induced ROS, Erk1/2 activation and apoptosis, whereas overexpression of constitutively active Akt (myr-Akt) conferred high resistance to the resveratrol's inhibitory effects in the neuronal cells. Taken together, the results indicate that resveratrol attenuates Cd-induced neuronal apoptosis partly through inhibition of mTORC1/2 pathways. Our studies highlight that resveratrol can be exploited for the prevention of Cd toxicity related to neurodegenerative diseases.
白藜芦醇是一种具有神经保护功能的天然多酚。其潜在机制尚不清楚。我们之前的研究已经确定,白藜芦醇通过靶向 PP2A/PP5 介导的 Erk1/2 和 JNK 通路拮抗镉 (Cd) 神经毒性。在这里,我们表明白藜芦醇通过阻断 Cd 诱导的 PC12 细胞和鼠原代神经元中 mTORC1 和 mTORC2 通路的激活来抵抗 Cd 中毒。用 mTORC1(雷帕霉素)、mTORC1/2(PP242)、Erk1/2(U0126)和/或 JNK(SP600125)抑制剂共同处理、敲低 mTOR 或沉默 Raptor、Rictor 或 Raptor/Rictor 分别破坏 mTORC1 和/或 mTORC2,显著增强了白藜芦醇对 Cd 诱导的 S6K1/4E-BP1(mTORC1 底物)、Akt(mTORC2 底物)、Erk1/2 和/或 JNK/c-Jun 磷酸化、caspase-3 切割和 PC12 细胞和/或原代神经元死亡的抑制作用。敲低 S6K1 或 4E-BP1,或过表达组成性低磷酸化 4E-BP1(4E-BP1-5A)增强了白藜芦醇对 Cd 诱导的细胞死亡的抑制作用,而过表达组成性活性 S6K1 或敲低 4E-BP1 减弱了白藜芦醇对 Cd 诱导的细胞死亡的抑制作用。用 Akt 抑制剂共同处理或过表达显性负性 Akt(dn-Akt)增强了白藜芦醇对 Cd 诱导的 ROS、Erk1/2 激活和细胞凋亡的抑制作用,而过表达组成性活性 Akt(myr-Akt)使神经元细胞对白藜芦醇的抑制作用具有很高的抗性。综上所述,这些结果表明,白藜芦醇通过抑制 mTORC1/2 通路减轻 Cd 诱导的神经元凋亡。我们的研究强调,白藜芦醇可用于预防与神经退行性疾病相关的 Cd 毒性。