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Autophagy captures the retromer-TBC1D5 complex to inhibit receptor recycling.
- Source :
-
Autophagy [Autophagy] 2024 Apr; Vol. 20 (4), pp. 863-882. Date of Electronic Publication: 2023 Nov 17. - Publication Year :
- 2024
-
Abstract
- Retromer prevents the destruction of numerous receptors by recycling them from endosomes to the trans- Golgi network or plasma membrane. This enables retromer to fine-tune the activity of many signaling pathways in parallel. However, the mechanism(s) by which retromer function adapts to environmental fluctuations such as nutrient withdrawal and how this affects the fate of its cargoes remains incompletely understood. Here, we reveal that macroautophagy/autophagy inhibition by MTORC1 controls the abundance of retromer <superscript>+</superscript> endosomes under nutrient-replete conditions. Autophagy activation by chemical inhibition of MTOR or nutrient withdrawal does not affect retromer assembly or its interaction with the RAB7 GAP protein TBC1D5, but rather targets these endosomes for bulk destruction following their capture by phagophores. This process appears to be distinct from amphisome formation. TBC1D5 and its ability to bind to retromer, but not its C-terminal LC3-interacting region (LIR) or nutrient-regulated dephosphorylation, is critical for retromer to be captured by autophagosomes following MTOR inhibition. Consequently, endosomal recycling of its cargoes to the plasma membrane and trans- Golgi network is impaired, leading to their lysosomal turnover. These findings demonstrate a mechanistic link connecting nutrient abundance to receptor homeostasis. Abbreviations : AMPK, 5'-AMP-activated protein kinase; APP, amyloid beta precursor protein; ATG, autophagy related; BafA, bafilomycin A <subscript>1</subscript> ; CQ, chloroquine; DMEM, Dulbecco's minimum essential medium; DPBS, Dulbecco's phosphate-buffered saline; EBSS, Earle's balanced salt solution; FBS, fetal bovine serum; GAP, GTPase-activating protein; MAP1LC3/LC3, microtubule associated protein 1 light chain 3; LIR, LC3-interacting region; LANDO, LC3-associated endocytosis; LP, leupeptin and pepstatin; MTOR, mechanistic target of rapamycin kinase; MTORC1, MTOR complex 1; nutrient stress, withdrawal of amino acids and serum; PDZ, DLG4/PSD95, DLG1, and TJP1/zo-1; RPS6, ribosomal protein S6; RPS6KB1/S6K1, ribosomal protein S6 kinase B1; SLC2A1/GLUT1, solute carrier family 2 member 1; SORL1, sortillin related receptor 1; SORT1, sortillin 1; SNX, sorting nexin; TBC1D5, TBC1 domain family member 5; ULK1, unc-51 like autophagy activating kinase 1; WASH, WASH complex subunit.
- Subjects :
- Humans
Autophagosomes metabolism
trans-Golgi Network metabolism
Mechanistic Target of Rapamycin Complex 1 metabolism
rab GTP-Binding Proteins metabolism
HeLa Cells
rab7 GTP-Binding Proteins
Vesicular Transport Proteins metabolism
Animals
TOR Serine-Threonine Kinases metabolism
Autophagy physiology
Endosomes metabolism
GTPase-Activating Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 1554-8635
- Volume :
- 20
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Autophagy
- Publication Type :
- Academic Journal
- Accession number :
- 37938196
- Full Text :
- https://doi.org/10.1080/15548627.2023.2281126