a Department of Biological Sciences , Rutgers University , Newark , NJ , USA.
b Telethon Institute of Genetics and Medicine (TIGEM) , Pozzuoli , Italy.
Autophagy. 2019 Jan;15(1):151-164. doi: 10.1080/15548627.2018.1511504. Epub 2018 Sep 10.
The mechanistic target of rapamycin kinase complex 1 (MTORC1) is a central cellular kinase that integrates major signaling pathways, allowing for regulation of anabolic and catabolic processes including macroautophagy/autophagy and lysosomal biogenesis. Essential to these processes is the regulatory activity of TFEB (transcription factor EB). In a regulatory feedback loop modulating transcriptional levels of RRAG/Rag GTPases, TFEB controls MTORC1 tethering to membranes and induction of anabolic processes upon nutrient replenishment. We now show that TFEB promotes expression of endocytic genes and increases rates of cellular endocytosis during homeostatic baseline and starvation conditions. TFEB-mediated endocytosis drives assembly of the MTORC1-containing nutrient sensing complex through the formation of endosomes that carry the associated proteins RRAGD, the amino acid transporter SLC38A9, and activate AKT/protein kinase B (AKT p-T308). TFEB-induced signaling endosomes en route to lysosomes are induced by amino acid starvation and are required to dissociate TSC2, re-tether and activate MTORC1 on endolysosomal membranes. This study characterizes TFEB-mediated endocytosis as a critical process leading to activation of MTORC1 and autophagic function, thus identifying the importance of the dynamic endolysosomal system in cellular clearance. Abbreviations: CAD: central adrenergic tyrosine hydroxylase-expressing-a-differentiated; ChIP-seq: chromosome immunoprecipitation sequencing; DAPI: 4',6-diamidino-2-phenylindole; DMSO: dimethyl sulfoxide; EDTA: ethylenediaminetetraacetic acid; EEA1: early endosomal antigen 1; EGF: epidermal growth factor; FBS: fetal bovine serum; GFP: green fluorescent protein; GTPase: guanosine triphosphatase; HEK293T: human embryonic kidney 293 cells expressing a temperature-sensitive mutant of the SV40 large T antigen; LAMP: lysosomal-associated membrane protein; LYNUS: lysosomal nutrient-sensing complex; MAP1LC3/LC3: microtubule associated protein 1 light chain 3 alpha/beta; MTOR: mechanistic target of rapamycin kinase; MTORC: mechanistic target of rapamycin kinase complex; OE: overexpression; PH: pleckstrin homology; PtdIns(3,4,5)P: phosphatidylinositol 3,4,5-trisphosphate; RRAGD: Ras related GTPase binding D; RHEB: Ras homolog enriched in brain; SLC38A9: solute carrier family 38 member 9; SQSTM1: sequestosome 1; TFEB: transcription factor EB; TSC2: tuberous sclerosis 2; TMR: tetramethylrhodamine; ULK1: unc-51 like kinase 1; WT: wild type.
雷帕霉素靶蛋白激酶复合物 1(MTORC1)的机械靶点是一种细胞内激酶,它整合了主要的信号通路,允许调节包括大分子自噬/自噬和溶酶体生物发生在内的合成代谢和分解代谢过程。TFEB(转录因子 EB)的调节活性对于这些过程至关重要。在调节 RRAG/Rag GTPase 转录水平的调节反馈回路中,TFEB 控制 MTORC1 与膜的连接,并在营养物质补充时诱导合成代谢过程。我们现在表明,TFEB 在稳态和饥饿条件下促进内吞基因的表达,并增加细胞内吞作用的速率。TFEB 介导的内吞作用通过形成携带相关蛋白 RRAGD、氨基酸转运蛋白 SLC38A9 和激活 AKT/蛋白激酶 B(AKT p-T308)的内体来促进 MTORC1 包含的营养感应复合物的组装。由氨基酸饥饿诱导的、用于向溶酶体传递的 TFEB 诱导的信号内体,需要分离 TSC2,重新连接并在内吞溶酶体膜上激活 MTORC1。这项研究将 TFEB 介导的内吞作用描述为导致 MTORC1 和自噬功能激活的关键过程,从而确定动态内吞体系统在细胞清除中的重要性。缩写词:CAD:中枢肾上腺素能酪氨酸羟化酶表达-a-分化;ChIP-seq:染色质免疫沉淀测序;DAPI:4',6-二脒基-2-苯基吲哚;DMSO:二甲基亚砜;EDTA:乙二胺四乙酸;EEA1:早期内体抗原 1;EGF:表皮生长因子;FBS:胎牛血清;GFP:绿色荧光蛋白;GTPase:鸟苷三磷酸酶;HEK293T:表达 SV40 大 T 抗原温度敏感突变的人胚肾 293 细胞;LAMP:溶酶体相关膜蛋白;LYNUS:溶酶体营养感应复合物;MAP1LC3/LC3:微管相关蛋白 1 轻链 3 alpha/beta;MTOR:雷帕霉素靶蛋白激酶;MTORC:雷帕霉素靶蛋白激酶复合物;OE:过表达;PH:pleckstrin 同源;PtdIns(3,4,5)P:磷脂酰肌醇 3,4,5-三磷酸;RRAGD:Ras 相关 GTP 结合 D;RHEB:富含脑的 Ras 同源物;SLC38A9:溶质载体家族 38 成员 9;SQSTM1:自噬体 1;TFEB:转录因子 EB;TSC2:结节性硬化症 2;TMR:四甲基罗丹明;ULK1:UNC-51 样激酶 1;WT:野生型。