Evidence map›Paper›PMID 40620085›Full record

ArticleJournal of extracellular vesicles2025

Small and Large Extracellular Vesicles From Human Preovulatory Follicular Fluid Display Distinct ncRNA Cargo Profiles and Differential Effects on KGN Granulosa Cells.

Inge Varik, Katariina Johanna Saretok, Kristine Rosenberg, Ileana Quintero, Maija Puhka, Nataliia Volkova, Aleksander Trošin, Paolo Guazzi, Agne Velthut-Meikas

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

9 citing papers in PubMed.

  1. 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

9 authors.

Inge VarikDepartment of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.ORCID https://orcid.org/0000-0003-1740-1022
Katariina Johanna SaretokDepartment of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.ORCID https://orcid.org/0009-0004-7370-5463
Kristine RosenbergDepartment of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.ORCID https://orcid.org/0009-0006-0504-2818
Ileana QuinteroHiPREP Core, Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID https://orcid.org/0000-0001-7040-1289
Maija PuhkaHiPREP Core, Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID https://orcid.org/0000-0002-6445-1017
Nataliia VolkovaDepartment of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.ORCID https://orcid.org/0000-0003-1832-6116
Aleksander TrošinEast Tallinn Central Hospital, Tallinn, Estonia.
Paolo GuazziHansaBioMed Life Sciences Ltd, Tallinn, Estonia.
Agne Velthut-MeikasDepartment of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.ORCID https://orcid.org/0000-0003-1927-9016

Funding

Alexander von Humboldt Foundation VA23021Eesti Teadusagentuur PSG608
6 · The paper itself

Abstract

Follicular fluid extracellular vesicles (FF EVs) facilitate communication between oocytes and somatic cells within the ovarian follicle, playing a pivotal role in follicular development. This study highlights the molecular and functional distinctions between small (SEV) and large (LEV) FF EV subpopulations, revealing their specialised regulatory roles in granulosa cell (GC) biology and their consequential impact on ovarian function. Single-EV profiling uncovered distinct tetraspanin distributions, with LEVs containing a lower proportion of CD9/CD63/CD81-positive particles compared to SEVs. Fluorescent labelling confirmed uptake of both SEVs and LEVs by GCs, supporting their capacity to impact cellular behaviour. Functionally, LEVs increased testosterone production by GCs, whilst SEVs had no effect on steroid hormone secretion, suggesting a specific role for LEVs in androgen biosynthesis. Transcriptomic analysis revealed extensive SEV-induced changes in GC gene expression, affecting pathways involved in transcription, TGF-β signalling, extracellular matrix (ECM) remodelling and cell cycle regulation. In contrast, LEVs elicited minimal transcriptional changes, primarily modulating genes associated with immune regulation and oxidative stress defence. Small RNA sequencing further revealed distinct non-coding RNA (ncRNA) profiles, with SEVs enriched in miRNAs targeting pathways critical for GC differentiation, whilst LEVs carried higher levels of piRNAs implicated in maintaining genomic stability. These findings advance our understanding of FF EV-mediated intercellular communication and underscore the importance of investigating EV subpopulations independently.

Indexed as

Extracellular VesiclesFollicular FluidGranulosa CellsRNA, UntranslatedAdultFemaleHumansRNA, Untranslatedextracellular vesiclesfollicular fluidgranulosa cellsmiRNAncRNAovary

Identifiers

PMID40620085
PMCPMC12230353

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.