Evidence map›Paper›PMID 36830648›Full record

ArticleBiomolecules2023

The Extracellular Vesicles Proteome of Endometrial Cells Simulating the Receptive Menstrual Phase Differs from That of Endometrial Cells Simulating the Non-Receptive Menstrual Phase.

Amber Rose Hart, Norhayati Liaqat Ali Khan, Keerthie Dissanayake, Kasun Godakumara, Aneta Andronowska, Saji Eapen, Paul R Heath, Alireza Fazeli

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  8. Extracellular vesicles: key mediators inFrontiers in veterinary science · 2025
    Review
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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 5 institutions in 5 countries.

Amber Rose HartAcademic Unit of Reproductive and Developmental Medicine, Department of Oncology and Metabolism, The Medical School, University of Sheffield, Jessop Wing, Tree Root Walk, Sheffield S10 2SF, UK.
Norhayati Liaqat Ali KhanFaculty of Dentistry, University Teknologi MARA (UiTM), Shah Alam 40450, Malaysia.
Keerthie DissanayakeDepartment of Pathophysiology, Institute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Ravila St. 14B, 50411 Tartu, Estonia.
Kasun GodakumaraDepartment of Pathophysiology, Institute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Ravila St. 14B, 50411 Tartu, Estonia.
Aneta AndronowskaInstitute of Animal Reproduction and Food Research, Polish Academy of Sciences, Juliana Tuwima St. 10, 10-748 Olsztyn, Poland.
Saji EapenSPD Development Co., Ltd., Clearblue Innovation Centre, Stannard Way, Priory Business Park, Bedford MK44 3UP, UK.
Paul R HeathDepartment of Neuroscience, University of Sheffield, Sheffield S10 2HQ, UK.ORCID 0000-0002-8385-1438
Alireza FazeliAcademic Unit of Reproductive and Developmental Medicine, Department of Oncology and Metabolism, The Medical School, University of Sheffield, Jessop Wing, Tree Root Walk, Sheffield S10 2SF, UK.
Estonian University of Life Sciences · EEUniversity of Sheffield · GBInLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences · PLUniversiti Teknologi MARA · MYUniversity of Peradeniya · LK

Funding

European Union's Horizon 2020 research and innovation programme under COMBIVET ERA Chair 857418
6 · The paper itself

Abstract

Successful embryo implantation into a receptive endometrium requires mutual endometrial-embryo communication. Recently, the function of extracellular vehicles (EVs) in cell-to-cell interaction in embryo-maternal interactions has been investigated. We explored isolated endometrial-derived EVs, using RL95-2 cells as a model of a receptive endometrium, influenced by the menstrual cycle hormones estrogen (E2; proliferative phase), progesterone (P4; secretory phase), and estrogen plus progesterone (E2P4; the receptive phase). EV sized particles were isolated by differential centrifugation and size exclusion chromatography. Nanoparticle tracking analysis was used to examine the different concentrations and sizes of particles and EV proteomic analysis was performed using shotgun label-free mass spectrometry. Our results showed that although endometrial derived EVs were secreted in numbers independent of hormonal stimulation, EV sizes were statistically modified by it. Proteomics analysis showed that hormone treatment changes affect the endometrial EV's proteome, with proteins enhanced within the EV E2P4 group shown to be involved in different processes, such as embryo implantation, endometrial receptivity, and embryo development, supporting the concept of a communication system between the embryo and the maternal endometrium via EVs.

Indexed as

Extracellular VesiclesProgesteroneEndometriumEstrogensFemaleHumansProteomeProteomicsEstrogensProgesteroneProteomeendometriumextracellular vesiclesfertilityproteomicsreceptivity

Identifiers

PMID36830648
PMCPMC9953153
OpenAlexW4319003765

What Socratic 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 Socratic graph.