Evidence map›Paper›PMID 32357161›Full record

ArticlePloS one2020

Functional cycle of EEA1-positive early endosome: Direct evidence for pre-existing compartment of degradative pathway.

Rimma Kamentseva, Vera Kosheverova, Marianna Kharchenko, Maria Zlobina, Anna Salova, Tatiana Belyaeva, Nikolay Nikolsky, Elena Kornilova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Microglia-derived extracellular vesicles trigger age-related neurodegeneration upon DNA damage.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. EGF, TGF-International journal of molecular sciences · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Rimma KamentsevaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Vera KosheverovaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Marianna KharchenkoInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Maria ZlobinaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Anna SalovaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Tatiana BelyaevaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Nikolay NikolskyInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.
Elena KornilovaInstitute of Cytology of the Russian Academy of Sciences, St. Petersburg, Russia.ORCID 0000-0002-2951-6292
Institute of Cytology · RUSt Petersburg University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early endosomes, regarded as the main sorting station on endocytic pathway, are characterized by high frequency of homotypic fusions mediated by tethering protein EEA1. Despite intensive investigations, biogenesis of endosomes, boundaries between early and late endosomes, and process of cargo transition though them remain obscure. Here, using EGF/EGFR endocytosis as a model and confocal microscopy of fixed and live cells, we provide evidence favoring EEA1-vesicles being pre-existed vesicular compartment, that maintains its resident proteins' level and is sensitive to biosynthetic, but not endocytic pathway disturbance. EEA1-vesicles directly fuse with incoming EGF/EGFR-vesicles into hybrid endosomes with separated EEA1- and EGFR-domains, thus providing a platform for rapid achievement of an excess of surface-derived membrane that is used to form intraluminal vesicles (ILVs). Thus, multivesicular structures colocalized with EEA1 are still early endosomes. "EEA1-cycle" ends by exclusion of EGFR-containing domains with ILVs inside that turns into MVE and restoration of initial EEA1-vesicles population.

Indexed as

Biosynthetic PathwaysCulture Media, Serum-FreeCytoplasmic VesiclesEndocytosisEndosomesErbB ReceptorsGreen Fluorescent ProteinsHeLa CellsHumansMicroscopy, ConfocalModels, BiologicalProtein TransportRecombinant Fusion ProteinsVesicular Transport ProteinsCulture Media, Serum-Freeearly endosome antigen 1EGFR protein, humanErbB ReceptorsGreen Fluorescent ProteinsRecombinant Fusion ProteinsVesicular Transport Proteins

Identifiers

PMID32357161
PMCPMC7194439
OpenAlexW3022289364

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.