Evidence map›Paper›PMID 39918406›Full record

ArticleeLife2025

A 'torn bag mechanism' of small extracellular vesicle release via limiting membrane rupture of en bloc released amphisomes (amphiectosomes).

Tamás Visnovitz, Dorina Lenzinger, Anna Koncz, Péter M Vizi, Tünde Bárkai, Krisztina V Vukman, Alicia Galinsoga, Krisztina Németh, Kelsey Fletcher, Zsolt I Komlósi and 5 more

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Condensates on the Move: Midbody Remnants as Large, Translation-Competent Extracellular Vesicles.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  5. Article
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  7. Article
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  11. Article
  12. Review
  13. Extracellular Vesicles: Biology and Therapeutic Applications.International journal of molecular sciences · 2024
    Article
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

15 authors.

Tamás Visnovitz *Semmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.ORCID https://orcid.org/0000-0002-7962-5083
Dorina Lenzinger *Semmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.ORCID https://orcid.org/0000-0003-0270-7985
Anna Koncz *Semmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Péter M ViziSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Tünde BárkaiSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Krisztina V VukmanSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Alicia GalinsogaSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Krisztina NémethSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Kelsey FletcherSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Zsolt I KomlósiSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Csaba CserépLaboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, Hungary.
Ádám DénesLaboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, Hungary.
Péter LőrinczELTE Eötvös Loránd University, Department of Anatomy, Cell and Developmental Biology, Budapest, Hungary.ORCID https://orcid.org/0000-0001-7374-667X
Gábor ValczSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.
Edit I BuzasSemmelweis University, Department of Genetics, Cell- and Immunobiology, Budapest, Hungary.ORCID https://orcid.org/0000-0002-3744-206X

Funding

Eotvos Lorand University Excellence Fund EKA 2022/045-P101European Commission 2019-2.1.7-ERA-NET-2021-00015Horizon 2020 Framework Programme 739593Hungarian Academy of Sciences János Bolyai Research ScholarshipHungarian Academy of Sciences LP2022-5/2022Hungarian Government and European Commission VEKOP-2.3.2-162016-00002Hungarian Government and European Commission VEKOP-2.3.3-15-2017-00016Hungary Academy of Sciences LP2022-13/2022NKFIH Advanced 150767NKFIH FK 138851NKFIH Higher Education Excellence Program (FIKP)NKFIH Hungarian Brain Research Program NAP2022-I-1/2022NKFIH K120237NKFIH K135637NKFIH NVKP_16-1-2016-0004NKFIH RRF-2.3.121-2022-00003NKFIH Therapeutic Thematic Programme TKP2021-EGA-23NKFIH ÚNKP-23-3-I-SE-2Semmelweis Innovation Fund STIA 2020 KFI
6 · The paper itself

Abstract

Recent studies showed an unexpected complexity of extracellular vesicle (EV) biogenesis pathways. We previously found evidence that human colorectal cancer cells in vivo release large multivesicular body-like structures en bloc. Here, we tested whether this large EV type is unique to colorectal cancer cells. We found that all cell types we studied (including different cell lines and cells in their original tissue environment) released multivesicular large EVs (MV-lEVs). We also demonstrated that upon spontaneous rupture of the limiting membrane of the MV-lEVs, their intraluminal vesicles (ILVs) escaped to the extracellular environment by a 'torn bag mechanism'. We proved that the MV-lEVs were released by ectocytosis of amphisomes (hence, we termed them amphiectosomes). Both ILVs of amphiectosomes and small EVs separated from conditioned media were either exclusively CD63 or LC3B positive. According to our model, upon fusion of multivesicular bodies with autophagosomes, fragments of the autophagosomal inner membrane curl up to form LC3B positive ILVs of amphisomes, while CD63 positive small EVs are of multivesicular body origin. Our data suggest a novel common release mechanism for small EVs, distinct from the exocytosis of multivesicular bodies or amphisomes, as well as the small ectosome release pathway.

Indexed as

Cell MembraneExtracellular VesiclesCell Line, TumorColorectal NeoplasmsHumansMicrotubule-Associated ProteinsMultivesicular BodiesTetraspanin 30Microtubule-Associated ProteinsTetraspanin 30amphisomeautophagybiogenesiscell biologyexosomesextracellular vesicleshumanmouseratsecretion

Identifiers

PMID39918406
PMCPMC11805505

What OpenQuestion holds

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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 OpenQuestion graph.