Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, China.
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Autophagy. 2021 Apr;17(4):872-887. doi: 10.1080/15548627.2020.1739442. Epub 2020 Mar 15.
Oxidative stress underlies a number of pathological conditions, including cancer, neurodegeneration, and aging. Antioxidant-rich foods help maintain cellular redox homeostasis and mitigate oxidative stress, but the underlying mechanisms are not clear. For example, sulforaphane (SFN), an electrophilic compound that is enriched in cruciferous vegetables such as broccoli, is a potent inducer of cellular antioxidant responses. NFE2L2/NRF2 (nuclear factor, erythroid 2 like 2), a transcriptional factor that controls the expression of multiple detoxifying enzymes through antioxidant response elements (AREs), is a proposed target of SFN. is a target gene of TFEB (transcription factor EB), a master regulator of autophagic and lysosomal functions, which we show here to be potently activated by SFN. SFN induces TFEB nuclear translocation via a Ca-dependent but MTOR (mechanistic target of rapamycin kinase)-independent mechanism through a moderate increase in reactive oxygen species (ROS). Activated TFEB then boosts the expression of genes required for autophagosome and lysosome biogenesis, which are known to facilitate the clearance of damaged mitochondria. Notably, TFEB activity is required for SFN-induced protection against both acute oxidant bursts and chronic oxidative stress. Hence, by simultaneously activating macroautophagy/autophagy and detoxifying pathways, natural compound SFN may trigger a self-defense cellular mechanism that can effectively mitigate oxidative stress commonly associated with many metabolic and age-related diseases. ANOVA: analyzes of variance; AREs: antioxidant response elements; Baf-A1: bafilomycin A; BHA: butylhydroxyanisole; CAT: catechin hydrate; CCCP: carbonyl cyanide m- chlorophenylhydrazone; CLEAR: coordinated lysosomal expression and regulation; DCFH-DA: 2',7'-dichlorofluorescin diacetate; FBS: fetal bovine serum; GFP: green fluorescent protein; HMOX1/HO-1: heme oxygenase 1; KD: knockdown; KEAP1: kelch like ECH associated protein 1; KO: knockout; LAMP1: lysosomal associated membrane protein 1; MCOLN1/TRPML1: mucolipin 1; ML-SA1: mucolipin-specific synthetic agonist 1; ML-SI3: mucolipin-specific synthetic inhibitor 3; MTOR: mechanistic target of rapamycin kinase; MTORC1: mechanistic target of rapamycin kinase complex 1; NAC: N-acetylcysteine; NFE2L2/NRF2: nuclear factor: erythroid 2 like 2; NPC: Niemann-Pick type C; PBS: phosphate-buffered saline; PPP2/PP2A: protein phosphatase 2; Q-PCR: real time polymerase chain reaction; ROS: reactive oxygen species; RPS6KB1/S6K1/p70S6K: ribosomal protein S6 kinase B1; SFN: sulforaphane; TFEB: transcription factor EB; WT, wild-type.
氧化应激是许多病理状况的基础,包括癌症、神经退行性疾病和衰老。富含抗氧化剂的食物有助于维持细胞氧化还原平衡并减轻氧化应激,但潜在机制尚不清楚。例如,西兰花等十字花科蔬菜中富含的具有反应活性的化合物萝卜硫素 (SFN),是细胞抗氧化反应的有效诱导剂。NFE2L2/NRF2(红细胞生成 2 样核因子)是一种转录因子,通过抗氧化反应元件 (ARE) 控制多种解毒酶的表达,被认为是 SFN 的靶点。TFEB(转录因子 EB)是自噬和溶酶体功能的主要调节因子,我们在这里显示它可以被 SFN 强烈激活,是 TFEB 是 TFEB 的靶基因。SFN 通过 Ca 依赖性但 MTOR(雷帕霉素靶蛋白激酶)非依赖性机制诱导 TFEB 核易位,该机制通过适度增加活性氧 (ROS) 来实现。激活的 TFEB 然后增强自噬体和溶酶体发生所需基因的表达,这已知有助于清除受损的线粒体。值得注意的是,SFN 诱导的保护作用需要 TFEB 活性,以抵抗急性氧化剂爆发和慢性氧化应激。因此,通过同时激活巨自噬/自噬和解毒途径,天然化合物 SFN 可能触发一种有效的自我防御细胞机制,可有效减轻与许多代谢和与年龄相关的疾病相关的氧化应激。ANOVA:方差分析;AREs:抗氧化反应元件;Baf-A1:巴弗霉素 A;BHA:丁基羟基茴香醚;CAT:儿茶素水合物;CCCP:羰基氰化物 m-氯苯腙;CLEAR:协调溶酶体表达和调节;DCFH-DA:2',7'-二氯荧光素二乙酸酯;FBS:胎牛血清;GFP:绿色荧光蛋白;HMOX1/HO-1:血红素加氧酶 1;KD:敲低;KEAP1:Kelch 样 ECH 相关蛋白 1;KO:敲除;LAMP1:溶酶体相关膜蛋白 1;MCOLN1/TRPML1:粘蛋白 1;ML-SA1:粘蛋白特异性合成激动剂 1;ML-SI3:粘蛋白特异性合成抑制剂 3;MTOR:雷帕霉素靶蛋白激酶;MTORC1:雷帕霉素靶蛋白激酶复合物 1;NAC:N-乙酰半胱氨酸;NFE2L2/NRF2:核因子:红细胞生成 2 样 2;NPC:尼曼-匹克 C 型;PBS:磷酸盐缓冲盐水;PPP2/PP2A:蛋白磷酸酶 2;Q-PCR:实时聚合酶链反应;ROS:活性氧;RPS6KB1/S6K1/p70S6K:核糖体蛋白 S6 激酶 B1;SFN:萝卜硫素;TFEB:转录因子 EB;WT,野生型。