Evidence map›Paper›PMID 35977488›Full record

ArticleCell reports2022

Endocytic membrane repair by ESCRT-III controls antigen export to the cytosol during antigen cross-presentation.

Marine Gros, Elodie Segura, Derek C Rookhuizen, Blandine Baudon, Sandrine Heurtebise-Chrétien, Nina Burgdorf, Mathieu Maurin, Eugene A Kapp, Richard J Simpson, Patrycja Kozik and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Restricted MHC-II trafficking inbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. WDFY4-dependent cross-presentation proceeds via a vacuolar antigen-processing route.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. VSVNature communications · 2024
    Article
  12. HNEAP Regulates Necroptosis of Cardiomyocytes by Suppressing the mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Channeling antigens to CD8Science (New York, N.Y.) · 2023
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 4 countries.

Marine GrosInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France. Electronic address: marine.mv.gros@gmail.com.
Elodie SeguraInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France; Department of Microbiology and Immunology at the Doherty Institute for Infection and Immunity, The University of Melbourne, Parkville, VIC 3010, Australia; Department of Biochemistry and Molecular Biology at the Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
Derek C RookhuizenInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Blandine BaudonInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Sandrine Heurtebise-ChrétienInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Nina BurgdorfInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Mathieu MaurinInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Eugene A KappWalter & Eliza Hall Institute of Medical Research, University of Melbourne, Melbourne, VIC 3052, Australia.
Richard J SimpsonDepartment of Biochemistry and Genetics, La Trobe Institute for Molecular Science (LIMS), La Trobe University, Melbourne, VIC 3086, Australia.
Patrycja KozikProtein & Nucleic Acid Chemistry Division, MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
Jose A VilladangosDepartment of Microbiology and Immunology at the Doherty Institute for Infection and Immunity, The University of Melbourne, Parkville, VIC 3010, Australia; Department of Biochemistry and Molecular Biology at the Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Parkville, VIC 3010, Australia.
Mathieu J M BertrandDepartment of Biomedical Molecular Biology, Ghent University, Technologiepark-Zwinjaarde 71, 9052 Zwinaarde-Ghent, Belgium; VIB Center for Inflammation Research, Technologiepark-Zwinjaarde 71, 9052 Zwinaarde-Ghent, Belgium.
Marianne BurbageInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France. Electronic address: marianne.burbage@curie.fr.
Sebastian AmigorenaInstitut Curie, PSL University, INSERM U932, Immunity and Cancer, 75005 Paris, France.
Inserm · FRThe University of Melbourne · AUAblynx (Belgium) · BELa Trobe University · AUMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_UP_1201/26Wellcome TrustWellcome Trust 101578/Z/13/Z
6 · The paper itself

Abstract

Despite its crucial role in initiation of cytotoxic immune responses, the molecular pathways underlying antigen cross-presentation remain incompletely understood. The mechanism of antigen exit from endocytic compartments into the cytosol is a long-standing matter of controversy, confronting two main models: transfer through specific channels/transporters or rupture of endocytic membranes and leakage of luminal content. By monitoring the occurrence of intracellular damage in conventional dendritic cells (cDCs), we show that cross-presenting cDC1s display more frequent endomembrane injuries and increased recruitment of endosomal sorting complex required for transport (ESCRT)-III, the main repair system for intracellular membranes, relative to cDC2s. Silencing of CHMP2a or CHMP4b, two effector subunits of ESCRT-III, enhances cytosolic antigen export and cross-presentation. This phenotype is partially reversed by chemical inhibition of RIPK3, suggesting that endocytic damage is related to basal activation of the necroptosis pathway. Membrane repair therefore proves crucial in containing antigen export to the cytosol and cross-presentation in cDCs.

Indexed as

Cross-PrimingEndosomal Sorting Complexes Required for TransportAntigen PresentationAntigensCytosolAntigensEndosomal Sorting Complexes Required for TransportCP: Cell biologyCP: Immunologycross-presentationdendritic cellsendomembrane disruptionESCRT-IIImembrane repairnecroptosis

Identifiers

PMID35977488
PMCPMC9396532
OpenAlexW4292056124

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.