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VPS37A directs ESCRT recruitment for phagophore closure
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4939-2309-0_12openalex-snapshot
Assessing Mammalian Autophagy
inferredcites →https://doi.org/10.1007/978-1-59745-157-4_2openalex-snapshot
Fine Structure of the Autophagosome
inferredcites →https://doi.org/10.1016/j.cell.2010.04.034openalex-snapshot
C. elegans Screen Identifies Autophagy Genes Specific to Multicellular Organisms
inferredcites →https://doi.org/10.1016/j.devcel.2008.08.013openalex-snapshot
Ordered Assembly of the ESCRT-III Complex on Endosomes Is Required to Sequester Cargo during MVB Formation
inferredcites →https://doi.org/10.1016/j.molcel.2010.09.023openalex-snapshot
Autophagy and the Integrated Stress Response
inferredcites →https://doi.org/10.1016/j.molcel.2016.08.021openalex-snapshot
The Vici Syndrome Protein EPG5 Is a Rab7 Effector that Determines the Fusion Specificity of Autophagosomes with Late Endosomes/Lysosomes
inferredcites →https://doi.org/10.1016/j.tibs.2016.08.016openalex-snapshot
Cellular Functions and Molecular Mechanisms of the ESCRT Membrane-Scission Machinery
inferredcites →https://doi.org/10.1016/s0092-8674(01)00434-2openalex-snapshot
Ubiquitin-Dependent Sorting into the Multivesicular Body Pathway Requires the Function of a Conserved Endosomal Protein Sorting Complex, ESCRT-I
inferredcites →https://doi.org/10.1038/cdd.2017.133openalex-snapshot
Atg2A/B deficiency switches cytoprotective autophagy to non-canonical caspase-8 activation and apoptosis
inferredcites →https://doi.org/10.1038/cr.2013.169openalex-snapshot
Historical landmarks of autophagy research
inferredcites →https://doi.org/10.1038/nature06639openalex-snapshot
Autophagy fights disease through cellular self-digestion
inferredcites →https://doi.org/10.1038/nature14503openalex-snapshot
ESCRT-III controls nuclear envelope reformation
inferredcites →https://doi.org/10.1038/nature20607openalex-snapshot
Designed proteins induce the formation of nanocage-containing extracellular vesicles
inferredcites →https://doi.org/10.1038/nbt.3235openalex-snapshot
Discovery of cancer drug targets by CRISPR-Cas9 screening of protein domains
inferredcites →https://doi.org/10.1038/nbt.3437openalex-snapshot
Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9
inferredcites →https://doi.org/10.1038/nmeth.3047openalex-snapshot
Improved vectors and genome-wide libraries for CRISPR screening
inferredcites →https://doi.org/10.1038/nmeth1089openalex-snapshot
A probability-based approach for the analysis of large-scale RNAi screens
inferredcites →https://doi.org/10.1038/nprot.2017.016openalex-snapshot
Genome-scale CRISPR-Cas9 knockout and transcriptional activation screening
inferredcites →https://doi.org/10.1038/nrm.2016.121openalex-snapshot
Reverse-topology membrane scission by the ESCRT proteins
inferredcites →https://doi.org/10.1038/nrm3696openalex-snapshot
The autophagosome: origins unknown, biogenesis complex
inferredcites →https://doi.org/10.1038/s41467-018-05254-wopenalex-snapshot
An autophagy assay reveals the ESCRT-III component CHMP2A as a regulator of phagophore closure
inferredcites →https://doi.org/10.1073/pnas.1005938107openalex-snapshot
Human ESCRT-III and VPS4 proteins are required for centrosome and spindle maintenance
inferredcites →https://doi.org/10.1073/pnas.1303360110openalex-snapshot
Thiazolidinediones are acute, specific inhibitors of the mitochondrial pyruvate carrier
inferredcites →https://doi.org/10.1074/jbc.m117.792747openalex-snapshot
Endophilin B2 facilitates endosome maturation in response to growth factor stimulation, autophagy induction, and influenza A virus infection
inferredcites →https://doi.org/10.1074/jbc.m405226200openalex-snapshot
The Human Endosomal Sorting Complex Required for Transport (ESCRT-I) and Its Role in HIV-1 Budding
inferredcites →https://doi.org/10.1080/15548627.2015.1091552openalex-snapshot
Autophagosome closure requires membrane scission
inferredcites →https://doi.org/10.1083/jcb.152.4.657openalex-snapshot
Dissection of Autophagosome Formation Using Apg5-Deficient Mouse Embryonic Stem Cells
inferredcites →https://doi.org/10.1083/jcb.200712064openalex-snapshot
FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells
inferredcites →https://doi.org/10.1083/jcb.200811130openalex-snapshot
ESCRT ubiquitin-binding domains function cooperatively during MVB cargo sorting
inferredcites →https://doi.org/10.1083/jcb.201507009openalex-snapshot
ALIX and ESCRT-I/II function as parallel ESCRT-III recruiters in cytokinetic abscission
inferredcites →https://doi.org/10.1083/jcb.201804132openalex-snapshot
Genome-wide CRISPR screen identifies TMEM41B as a gene required for autophagosome formation
inferredcites →https://doi.org/10.1083/jcb.201811173openalex-snapshot
Rab5-dependent autophagosome closure by ESCRT
inferredcites →https://doi.org/10.1091/mbc.e04-03-0250openalex-snapshot
The Growth-Regulatory Protein HCRP1/hVps37A Is a Subunit of Mammalian ESCRT-I and Mediates Receptor Down-Regulation
inferredcites →https://doi.org/10.1093/emboj/21.10.2397openalex-snapshot
Structure and functional interactions of the Tsg101 UEV domain
inferredcites →https://doi.org/10.1093/nar/18.12.3587openalex-snapshot
Advanced mammalian gene transfer: high titre retroviral vectors with multiple drug selection markers and a complementary helper-free packaging cell line
inferredcites →https://doi.org/10.1096/fj.201800975rrropenalex-snapshot
SCAP knockdown in vascular smooth muscle cells alleviates atherosclerosis plaque formation via up‐regulating autophagy in ApoE −/− mice
inferredcites →https://doi.org/10.1126/science.aar5078openalex-snapshot
Triggered recruitment of ESCRT machinery promotes endolysosomal repair
inferredcites →https://doi.org/10.1146/annurev-biochem-072909-101058openalex-snapshot
Membrane Fission Reactions of the Mammalian ESCRT Pathway
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154005openalex-snapshot
The Role of Atg Proteins in Autophagosome Formation
inferredcites →https://doi.org/10.1159/000373980openalex-snapshot
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
inferredcites →https://doi.org/10.1186/1475-2859-4-21openalex-snapshot
Structural genomics of human proteins – target selection and generation of a public catalogue of expression clones
inferredcites →https://doi.org/10.1242/jcs.050021openalex-snapshot
How do ESCRT proteins control autophagy?
inferredcites →https://doi.org/10.1242/jcs.091702openalex-snapshot
Induction of autophagy in ESCRT mutants is an adaptive response for cell survival in C. elegans
inferredcites →https://doi.org/10.1242/jcs.132415openalex-snapshot
Dynamic association of the ULK1 complex with omegasomes during autophagy induction
inferredcites →https://doi.org/10.1371/journal.pgen.1003715openalex-snapshot
Global Analysis of Fission Yeast Mating Genes Reveals New Autophagy Factors
inferredcites →https://doi.org/10.1371/journal.pone.0092845openalex-snapshot
Cellular Processing of Myocilin
inferredcites →https://doi.org/10.15252/embj.201695148openalex-snapshot
VCP/p97 cooperates with YOD1, UBXD1 and PLAA to drive clearance of ruptured lysosomes by autophagy
inferredcites →https://doi.org/10.15252/embj.201899753openalex-snapshot
ESCRT‐mediated lysosome repair precedes lysophagy and promotes cell survival
inferredcites →https://doi.org/10.4161/auto.4451openalex-snapshot
Dissection of the Autophagosome Maturation Process by a Novel Reporter Protein, Tandem Fluorescent-Tagged LC3
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Molecular and mesoscopic geometries in autophagosome generation. A review
inferred← citeshttps://doi.org/10.1016/j.ceb.2020.06.002openalex-snapshot
ESCRT puts its thumb on the nanoscale: Fixing tiny holes in endolysosomes
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Organelle homeostasis requires ESCRTs
inferred← citeshttps://doi.org/10.1016/j.ceb.2025.102493openalex-snapshot
Advances in mitophagy initiation mechanisms
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115016openalex-snapshot
Unveiling the physiological impact of ESCRT-dependent autophagosome closure by targeting the VPS37A ubiquitin E2 variant-like domain
inferred← citeshttps://doi.org/10.1016/j.cub.2022.11.002openalex-snapshot
Orchestration of selective autophagy by cargo receptors
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.05.016openalex-snapshot
Transferrin receptor controls both autophagosome formation and closure via phosphatidylinositol 3-phosphate synthesis
inferred← citeshttps://doi.org/10.1016/j.fct.2019.111075openalex-snapshot
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HRS sustains mitochondrial homeostasis by anchoring destabilized proteins during tumorigenesis
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The green ESCRTs: Newly defined roles for ESCRT proteins in plants
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Where and how do mammalian cells shape autophagosomes?
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DBeQ derivative targets vacuolar protein sorting 4 functions in cancer cells and suppresses tumor growth in mice
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Autophagy in liver diseases: A review
inferred← citeshttps://doi.org/10.1016/j.matbio.2021.01.001openalex-snapshot
Amino acid sensory complex proteins in mTORC1 and macroautophagy regulation
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.02.027openalex-snapshot
Protein degradation on the global scale
inferred← citeshttps://doi.org/10.1016/j.molcel.2026.04.031openalex-snapshot
TRIM21 induces selective autophagy of viruses and bacteria
inferred← citeshttps://doi.org/10.1038/s41417-026-01054-3openalex-snapshot
VPS37A loss creates CASP8-dependent vulnerability via the MAP3K7–NF-κB–CFLAR axis
inferred← citeshttps://doi.org/10.1038/s41418-020-00610-0openalex-snapshot
Targeting the ESCRT-III component CHMP2A for noncanonical Caspase-8 activation on autophagosomal membranes
inferred← citeshttps://doi.org/10.1038/s41419-025-07436-zopenalex-snapshot
Inactivation of necroptosis-promoting protein MLKL creates a therapeutic vulnerability in colorectal cancer cells
inferred← citeshttps://doi.org/10.1038/s41467-023-36132-9openalex-snapshot
ESCRT-dependent STING degradation inhibits steady-state and cGAMP-induced signalling
inferred← citeshttps://doi.org/10.1038/s41467-023-37185-6openalex-snapshot
The plant unique ESCRT component FREE1 regulates autophagosome closure
inferred← citeshttps://doi.org/10.1038/s41467-024-49485-6openalex-snapshot
Arabidopsis CaLB1 undergoes phase separation with the ESCRT protein ALIX and modulates autophagosome maturation
inferred← citeshttps://doi.org/10.1038/s41467-025-64800-5openalex-snapshot
Lysosomal and mTORC1 signaling dysregulation underpin the pathology of spastic paraplegia type 80
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Autophagosome biogenesis comes out of the black box
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Mechanisms governing autophagosome biogenesis
inferred← citeshttps://doi.org/10.1038/s41580-021-00392-4openalex-snapshot
Machinery, regulation and pathophysiological implications of autophagosome maturation
inferred← citeshttps://doi.org/10.1038/s41580-025-00909-1openalex-snapshot
ESCRT-III function in membrane fission and repair
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Regulation and roles of mammalian mitophagy
inferred← citeshttps://doi.org/10.1038/s41586-025-08950-yopenalex-snapshot
The expanding repertoire of ESCRT functions in cell biology and disease
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A helical assembly of human ESCRT-I scaffolds reverse-topology membrane scission
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Structure and activation of the human autophagy-initiating ULK1C:PI3KC3-C1 supercomplex
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Identification of membrane curvature sensing motifs essential for VPS37A phagophore recruitment and autophagosome closure
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Parallel CRISPR screens reveal pathways controlling the cell surface levels of the attractant receptor FPR1
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Molecular mechanisms of mammalian autophagy
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Cutting edge: ESCRT-mediated phagophore closure in mammals
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In vitro reconstitution of autophagic processes
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Molecular regulation of autophagosome formation
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
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Dysfunction of autophagy in high-fat diet-induced non-alcoholic fatty liver disease
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ER stress elicits non-canonical CASP8 (caspase 8) activation on autophagosomal membranes to induce apoptosis
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Removal of hypersignaling endosomes by simaphagy
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GORASP2 promotes phagophore closure and autophagosome maturation into autolysosomes
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USP8 promotes intracellular infection by enhancing ESCRT-mediated membrane repair, limiting xenophagy, and reducing oxidative stress
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Blocking autophagosome closure manifests the roles of mammalian Atg8-family proteins in phagophore formation and expansion during nutrient starvation
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Classical swine fever virus hijacks ESCRT-III and VPS4A to promote phagophore closure for accelerating mitophagy
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A novel autophagy inhibitor, bTBT, disturbs autophagosome formation
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The multifaceted role of autophagy and mitophagy in cardiovascular health and disease
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Plant autophagosomes mature into amphisomes prior to their delivery to the central vacuole
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Transcription factor Nrf1 regulates proteotoxic stress-induced autophagy
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ATG9A facilitates the closure of mammalian autophagosomes
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Conserved components of the macroautophagy machinery in Caenorhabditis elegans
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Molecular Mechanism of Autophagy, Cytoplasmic Zoning by Lipid Membranes
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GFS9 Affects Piecemeal Autophagy of Plastids in Young Seedlings ofArabidopsis thaliana
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ESCRT-dependent STING degradation curtails steady-state and cGAMP-induced signaling
inferred← citeshttps://doi.org/10.1101/2022.11.01.514784openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2023.04.22.537920openalex-snapshot
ESCRT disruption provides evidence against signaling functions for synaptic exosomes
inferred← citeshttps://doi.org/10.1101/2025.10.10.681573openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/mmi.15075openalex-snapshot
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Assessing methods to quantitatively validate TGFβ-dependent autophagy
inferred← citeshttps://doi.org/10.1242/jcs.250951openalex-snapshot
Concurrent depletion of Vps37 proteins evokes ESCRT-I destabilization and profound cellular stress responses
inferred← citeshttps://doi.org/10.1242/jcs.260943openalex-snapshot
Adaptations of membrane trafficking in cancer and tumorigenesis
inferred← citeshttps://doi.org/10.1360/ssv-2026-0054openalex-snapshot
The membrane localization mechanisms and functions of ATG8 family proteins in autophagic and non-autophagic pathways
inferred← citeshttps://doi.org/10.15252/embj.2019102586openalex-snapshot
ESCRT machinery mediates selective microautophagy of endoplasmic reticulum in yeast
inferred← citeshttps://doi.org/10.15252/embj.2020106922openalex-snapshot
Sealing holes in cellular membranes
inferred← citeshttps://doi.org/10.15252/embj.2022112845openalex-snapshot
Mammalian ATG8 proteins maintain autophagosomal membrane integrity through ESCRTs
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A conserved ATG2‐GABARAP family interaction is critical for phagophore formation
inferred← citeshttps://doi.org/10.21248/gups.67332openalex-snapshot
Minimized combinatorial CRISPR screens identify genetic interactions in autophagy
inferred← citeshttps://doi.org/10.32604/biocell.2022.018197openalex-snapshot
Recent biomedical advances enabled by HaloTag technology
inferred← citeshttps://doi.org/10.3389/fgene.2022.936292openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2021.691881openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fneur.2022.951536openalex-snapshot
Research progress on astrocyte autophagy in ischemic stroke
inferred← citeshttps://doi.org/10.3389/fonc.2021.632956openalex-snapshot
Mechanobiology of Autophagy: The Unexplored Side of Cancer
inferred← citeshttps://doi.org/10.3389/fonc.2022.1007446openalex-snapshot
The endosomal sorting complex required for transport repairs the membrane to delay cell death
inferred← citeshttps://doi.org/10.3389/fpls.2020.00565openalex-snapshot
Recent Advances in Membrane Shaping for Plant Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.3389/ftubr.2023.1275882openalex-snapshot
Atg8ylation as a host-protective mechanism against Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.3390/antiox12071425openalex-snapshot
Autophagy, Oxidative Stress, and Alcoholic Liver Disease: A Systematic Review and Potential Clinical Applications
inferred← citeshttps://doi.org/10.3390/brainsci12020247openalex-snapshot
Specific microRNAs for Modulation of Autophagy in Spinal Cord Injury
inferred← citeshttps://doi.org/10.3390/cells10071678openalex-snapshot
Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia
inferred← citeshttps://doi.org/10.3390/cells10112814openalex-snapshot
Key Regulators of Autophagosome Closure
inferred← citeshttps://doi.org/10.3390/cells13010103openalex-snapshot
Neuronal Autophagy: Regulations and Implications in Health and Disease
inferred← citeshttps://doi.org/10.3390/cells13060500openalex-snapshot
Molecular Mechanism of Autophagosome–Lysosome Fusion in Mammalian Cells
inferred← citeshttps://doi.org/10.3390/cells15020102openalex-snapshot
From Hero to Hijacker: Autophagy’s Double Life in Immune Patrols and Cancer Escape
inferred← citeshttps://doi.org/10.3390/cells9040831openalex-snapshot
Mitophagy in the Pathogenesis of Liver Diseases
inferred← citeshttps://doi.org/10.3390/covid4090095openalex-snapshot
ESCRT Protein VPS4A Is Required for the Formation of Replication Centers and Replication of Human Coronavirus 229E (HCoV-229E)
inferred← citeshttps://doi.org/10.3390/ijms21124506openalex-snapshot
Nucleophagy—Implications for Microautophagy and Health
inferred← citeshttps://doi.org/10.3390/ijms232315109openalex-snapshot
Natural-Product-Mediated Autophagy in the Treatment of Various Liver Diseases
inferred← citeshttps://doi.org/10.3390/membranes12060633openalex-snapshot
The ESCRT Machinery: Remodeling, Repairing, and Sealing Membranes
inferred← citeshttps://doi.org/10.37247/pacr.1.2021.40openalex-snapshot
Mechanobiology of Autophagy: The Unexplored Side of Cancer
inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-23-02068openalex-snapshot
Spastin and alsin protein interactome analyses begin to reveal key canonical pathways and suggest novel druggable targets
inferred← citeshttps://doi.org/10.64898/2026.09.03.749311openalex-snapshot
PCDH17 regulates lysosomal degradative capacity to promote autophagy attenuation during prolonged starvation
inferred← citeshttps://doi.org/10.70675/7104d6d5z945ez494eza917zda9e6be1eea6openalex-snapshot
Interaction entre autophagie et exosomes au niveau synaptique dans la maladie de Parkinson
inferred← citeshttps://doi.org/10.70675/899d5d97z1062z453cza091zcae756198817openalex-snapshot
Autophagy in the interplay between shear stress and kidney epithelium homeostasis
inferred← citeshttps://doi.org/10.70675/92766df5z1811z4470z97f3ze6b8287ff2dbopenalex-snapshot
Analyse des fonctions de la protéine du réticulum endoplasmique, PDZD-8 dans l'autophagie chez Caenorhabditis elegans
inferred← citeshttps://doi.org/10.7554/elife.100928openalex-snapshot
Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function
inferred← citeshttps://doi.org/10.7554/elife.100928.1openalex-snapshot
Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function
inferred← citeshttps://doi.org/10.7554/elife.100928.2openalex-snapshot
Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function
inferred← citeshttps://doi.org/10.7554/elife.100928.3openalex-snapshot
Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function
inferred← citeshttps://doi.org/10.7554/elife.102667openalex-snapshot
Target protein identification in live cells and organisms with a non-diffusive proximity tagging system
inferred← citeshttps://doi.org/10.7554/elife.102667.1openalex-snapshot
Target protein identification in live cells and organisms with a non-diffusive proximity tagging system
inferred← citeshttps://doi.org/10.7554/elife.102667.2openalex-snapshot
Target protein identification in live cells and organisms with a non-diffusive proximity tagging system
inferred← citeshttps://doi.org/10.7554/elife.102667.3openalex-snapshot
Target protein identification in live cells and organisms with a non-diffusive proximity tagging system
inferred← citeshttps://doi.org/10.7554/elife.85727openalex-snapshot
A TRAF-like E3 ubiquitin ligase TrafE coordinates ESCRT and autophagy in endolysosomal damage response and cell-autonomous immunity to Mycobacterium marinum
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