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Updated: Feb 6, 2026

Live Cell Imaging of Early Autophagy Events: Omegasomes and Beyond
Published on: July 27, 2013
TFEB-driven endocytosis coordinates MTORC1 signaling and autophagy
Israel C Nnah1, Biao Wang1, Chaitali Saqcena1
1a Department of Biological Sciences , Rutgers University , Newark , NJ , USA.
Abstract:
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)P3: 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.
Insights
Transcription factor EB (TFEB) enhances cellular endocytosis, driving the assembly of the MTORC1 complex. This process is crucial for nutrient sensing and activating autophagy, highlighting the endolysosomal system's role in cellular clearance.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Mechanistic target of rapamycin kinase complex 1 (MTORC1) regulates cellular anabolism and catabolism, including autophagy and lysosomal biogenesis.
- Transcription factor EB (TFEB) is a key regulator of these processes, influencing MTORC1 activity and lysosomal function.
Purpose of the Study:
- To investigate the role of TFEB in cellular endocytosis.
- To elucidate the mechanism by which TFEB-mediated endocytosis impacts MTORC1 activation and nutrient sensing.
Main Methods:
- Assessed TFEB's effect on endocytic gene expression and cellular endocytosis rates under homeostatic and starvation conditions.
- Utilized co-immunoprecipitation and microscopy to analyze the formation of TFEB-induced signaling endosomes and their association with MTORC1 components (RRAGD, SLC38A9, AKT).
- Investigated the role of these endosomes in MTORC1 activation by examining TSC2 dissociation and MTORC1 re-tethering to endolysosomal membranes.
Main Results:
- TFEB significantly promotes the expression of endocytic genes and increases endocytosis rates.
- TFEB-mediated endocytosis facilitates the assembly of a nutrient-sensing complex containing MTORC1, RRAGD, SLC38A9, and activated AKT.
- TFEB-induced signaling endosomes, upon amino acid starvation, are essential for MTORC1 activation on endolysosomal membranes by promoting TSC2 dissociation and MTORC1 re-tethering.
Conclusions:
- TFEB-mediated endocytosis is a critical pathway for activating MTORC1 signaling.
- This process is vital for nutrient sensing and subsequent autophagic function.
- The study underscores the importance of the dynamic endolysosomal system in maintaining cellular homeostasis and clearance.
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