MicroRNA-146b negatively affects bovine embryo development and quality.


Journal

Reproduction (Cambridge, England)
ISSN: 1741-7899
Titre abrégé: Reproduction
Pays: England
ID NLM: 100966036

Informations de publication

Date de publication:
01 Dec 2023
Historique:
received: 25 04 2023
accepted: 08 12 2023
medline: 8 12 2023
pubmed: 8 12 2023
entrez: 8 12 2023
Statut: aheadofprint

Résumé

MicroRNAs (miRNAs), which can be carried inside extracellular vesicles (EVs), play a crucial role in regulating embryo development up to the blastocyst stage. Yet, the molecular mechanisms underlying blastocyst development and quality are largely unknown. Recently, our group identified 69 differentially expressed miRNAs in extracellular vesicles (EVs) isolated from culture medium conditioned by bovine embryos that either developed to the blastocyst stage or did not (non-blastocysts). We found miR-146b to be more abundant in the EVs derived from media conditioned by non-blastocyst embryos. Using RT-qPCR, we here confirmed the upregulation of miR-146b in non-blastocyst (arrested at 2-4 cell and morula stage) embryos compared to blastocysts (p<0.005), which coincides with the upregulation of miR-146b in EVs derived from the medium of these non-blastocysts. To evaluate a functional effect, bovine embryo culture media were supplemented with miR-146b mimics, resulting in significantly decreased embryo quality, with lower blastocyst rates at day 7 and lower total cell numbers, while the opposite was found after supplementation with miR-146b inhibitors, which resulted in reduced apoptosis rates (P < 0.01). Transcriptomic analysis of embryos treated with miR-146b mimics or inhibitors showed differential expression (P < 0.01) of genes associated with apoptosis, cell differentiation, and the RNA Pol II transcription complex, including WDR36, MBNL2, ERCC6l2, PYGO1, and SNIP1. Overall, miR-146b is overexpressed in non-blastocyst embryos and in EVs secreted by these embryos, and it regulates genes involved in embryo development and apoptosis, resulting in decreased embryo quality.

Identifiants

pubmed: 38063339
doi: 10.1530/REP-23-0155
pii: REP-23-0155
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Krishna Chaitanya Pavani (KC)

K Pavani, Department of Internal Medicine, Reproduction and Population Medicine, University of Ghent, Gent, Belgium.

Guan XueFeng (G)

G XueFeng, Department of Nutrition, Genetics and Ethology, Ghent University, Merelbeke, Belgium.

Jayendra Chunduru (J)

J Chunduru, Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, United States.

Tim Meese (T)

T Meese, Department of Pharmaceutics, Ghent University, Gent, Belgium.

Luc J Peelman (LJ)

L Peelman, Nutrition, Genetics and Ethology, Ghent University, Gent, Belgium.

Filip Van Nieuwerburgh (F)

F Van Nieuwerburgh, Department of Pharmaceutics, Ghent University, Gent, Belgium.

Dieter Deforce (D)

D Deforce, Department of Pharmaceutics, Ghent University, Gent, Belgium.

An Hendrix (A)

A Hendrix, Department of Human Structure and Repair, University Hospital Ghent, Gent, Belgium.

Kelly Tilleman (K)

K Tilleman, Reproductive Medicine, University Hospital Ghent, Gent, Belgium.

Ann Van Soom (A)

A Van Soom, Department of Internal Medicine, Reproduction and Population Medicine, Ghent University, Merelbeke, Belgium.

Katrien Smits (K)

K Smits, Department of Internal Medicine, Reproduction and Population Medicine, University of Ghent, Gent, Belgium.

Classifications MeSH