Modulation of bovine oocyte developmental competence through exogenous miRNA delivered via engineered EVs

Clicks: 2
ID: 338963
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #189 of 189 articles by views in biology of reproduction

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 189 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
In vitro maturation (IVM) of oocytes plays a crucial role in assisted reproductive technologies in livestock production, enabling efficient large-scale embryos production and supporting genetics improvement programs. However, the efficiency of this technology remains limited as only a small proportion of cumulus-oocytes complexes (COCs) matured in vitro reach the blastocyst stage, which exhibit lower quality than those produced in vivo. Recent efforts have focused on delivering biological materials to cumulus cells during IVM to improve oocyte quality. Herein, we hypothesized that extracellular vesicles (EVs) isolated from ovarian follicular fluid (FF) can be engineered to deliver synthetic microRNAs (miRNAs) to cumulus cells during IVM. Here, we demonstrate for the first time that follicular fluid-derived EVs are enriched with synthetic miRNAs and successfully delivered to COCs, resulting in altered gene expression in cumulus cells, and transfer of miRNAs to the oocyte cytoplasm. Specifically, EVs loaded with bta-miR-20a-5p were effectively taken up by cumulus cells during IVM, enhanced PI3K/AKT signaling with significant increase in downstream genes, such EIF4b and GSK3, which are involved in cell cycle progression, DNA repair and protein synthesis. Additionally, bta-miR-20a-5p-loaded-EVs supplementation to COCs, during IVM, appeared to reduce cleavage and blastocyst development rates. Collectively, our findings demonstrated that engineered EVs can deliver a synthetic miRNA to COCs during IVM, representing highlighting their potential to modulate oocyte cytoplasm content and embryo development.
Reference Key
openalex_W7225336701 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors
Journal biology of reproduction
Year 2026
DOI
10.1093/biolre/ioag249
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.