Bovine oocyte developmental competence and gene expression following co-culturing with ampullary cells: An experimental study.

Bovine Fertilization Gene expression IVM. Ampulla

Journal

International journal of reproductive biomedicine
ISSN: 2476-4108
Titre abrégé: Int J Reprod Biomed
Pays: Iran
ID NLM: 101679102

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 12 02 2020
revised: 09 08 2020
accepted: 30 09 2020
entrez: 17 5 2021
pubmed: 18 5 2021
medline: 18 5 2021
Statut: epublish

Résumé

There is no sufficient information on the impact of bovine ampullary oviductal epithelial cells (BAOECs) on in vitro oocyte maturation competence and gene expression. This study aimed to examine the oocyte developmental competence following co-culturing with a monolayer of fresh and frozen-thawed ampullary cells. Bovine cumulus-oocyte complexes (COCs) were distributed into three groups: control group; where in COCs were cultured in cell-free media for 24 hr and FML and FTML groups in which the COCs were cultured in maturation media for 18 hr and then transferred into a media containing fresh and frozen-thawed BAOECs monolayer, respectively (BAOECs were extracted from the oviducts of slaughtered cattle and were then cultured freshly or frozen-thawed) for a further 6 hr. After 24 hr, the expanded COCs were evaluated for nuclear maturation, fertilization rate, and gene expression ( Nuclear maturation rate in the FTML group was significantly higher than the control group (p = 0.02). The fertilization rate of FTML group was significantly higher than the control and FML groups (p = 0.05 and p = 0.03, respectively). In terms of gene expression, Ampullary cells co-culturing (especially frozen-thawed cells) for in vitro maturation of bovine oocytes yields encourages the results and demonstrates the beneficial effect of co-culture on gene expression and developmental competence.

Sections du résumé

BACKGROUND BACKGROUND
There is no sufficient information on the impact of bovine ampullary oviductal epithelial cells (BAOECs) on in vitro oocyte maturation competence and gene expression.
OBJECTIVE OBJECTIVE
This study aimed to examine the oocyte developmental competence following co-culturing with a monolayer of fresh and frozen-thawed ampullary cells.
MATERIALS AND METHODS METHODS
Bovine cumulus-oocyte complexes (COCs) were distributed into three groups: control group; where in COCs were cultured in cell-free media for 24 hr and FML and FTML groups in which the COCs were cultured in maturation media for 18 hr and then transferred into a media containing fresh and frozen-thawed BAOECs monolayer, respectively (BAOECs were extracted from the oviducts of slaughtered cattle and were then cultured freshly or frozen-thawed) for a further 6 hr. After 24 hr, the expanded COCs were evaluated for nuclear maturation, fertilization rate, and gene expression (
RESULTS RESULTS
Nuclear maturation rate in the FTML group was significantly higher than the control group (p = 0.02). The fertilization rate of FTML group was significantly higher than the control and FML groups (p = 0.05 and p = 0.03, respectively). In terms of gene expression,
CONCLUSION CONCLUSIONS
Ampullary cells co-culturing (especially frozen-thawed cells) for in vitro maturation of bovine oocytes yields encourages the results and demonstrates the beneficial effect of co-culture on gene expression and developmental competence.

Identifiants

pubmed: 33997596
doi: 10.18502/ijrm.v19i4.9063
pmc: PMC8106812
doi:

Types de publication

Journal Article

Langues

eng

Pagination

371-380

Informations de copyright

Copyright © 2021 Azari et al.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Références

Biol Reprod. 2009 Aug;81(2):267-74
pubmed: 19299315
Vet Res Commun. 2017 Mar;41(1):49-56
pubmed: 27943152
Theriogenology. 2017 Jan 15;88:207-214
pubmed: 28234231
Proc Natl Acad Sci U S A. 2008 Oct 14;105(41):15809-14
pubmed: 18838686
Reproduction. 2015 Jan;149(1):R1-R14
pubmed: 25190504
Theriogenology. 2019 Mar 1;126:222-229
pubmed: 30590243
Gene. 2018 Sep 5;670:22-30
pubmed: 29802994
Reproduction. 2012 Dec;144(6):649-60
pubmed: 23028122
Reprod Biol. 2016 Mar;16(1):61-9
pubmed: 26952755
Theriogenology. 2009 Apr 1;71(6):939-46
pubmed: 19150733
Theriogenology. 2007 Sep 1;68 Suppl 1:S91-7
pubmed: 17512044
Asian J Androl. 2011 Mar;13(2):287-91
pubmed: 21076439
J Assist Reprod Genet. 2017 Jul;34(7):929-938
pubmed: 28386814
J Assist Reprod Genet. 2009 Mar;26(2-3):129-35
pubmed: 19184398
Int J Reprod Biomed. 2019 Sep 22;17(9):621-628
pubmed: 31646256
Transplantation. 2010 Mar 15;89(5):509-17
pubmed: 20125064
Theriogenology. 2017 Oct 15;102:29-34
pubmed: 28735105
Theriogenology. 2018 Jan 1;105:66-74
pubmed: 28923708
Reproduction. 2017 Apr;153(4):461-470
pubmed: 28104825
Mol Hum Reprod. 2009 Jun;15(6):321-33
pubmed: 19321517
Reprod Domest Anim. 2016 Sep;51 Suppl 1:37-45
pubmed: 27670939
Zygote. 2019 Oct;27(5):337-346
pubmed: 31405390
PLoS One. 2016 Feb 04;11(2):e0148083
pubmed: 26845570
Biol Reprod. 2013 Sep 19;89(3):56
pubmed: 23843241
Mol Reprod Dev. 2010 Apr;77(4):353-62
pubmed: 20043319

Auteurs

Mehdi Azari (M)

Department of Anatomical Sciences, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Department of Animal Reproduction, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Mojtaba Kafi (M)

Department of Animal Reproduction, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Anise Asaadi (A)

Department of Animal Reproduction, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Zohreh Pakniat (Z)

Department of Animal Reproduction, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Beheshteh Abouhamzeh (B)

Department of Anatomical Sciences, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.

Classifications MeSH