Membrane remodulation and hyperactivation are impaired in frozen-thawed sperm of low-fertility bulls.

Acrosome reaction CASA Field fertility Frozen-thawed semen Phosphorylated tyrosine

Journal

Theriogenology
ISSN: 1879-3231
Titre abrégé: Theriogenology
Pays: United States
ID NLM: 0421510

Informations de publication

Date de publication:
01 Jan 2023
Historique:
received: 19 08 2022
revised: 16 10 2022
accepted: 18 10 2022
pubmed: 5 11 2022
medline: 23 11 2022
entrez: 4 11 2022
Statut: ppublish

Résumé

Bulls used in artificial insemination programmes worldwide undergo quality control checks, which are typically based on the evaluation of sperm motility and morphology. Despite this, some bulls can have lower than expected field fertility and the reasons for this remain to be elucidated. Here we hypothesised that sperm from bulls of varying fertility will differ in their ability to undergo capacitation-related events including an increase in membrane fluidity, protein tyrosine phosphorylation, hyperactivation and the acrosome reaction. Firstly, we used frozen-thawed semen from 10 high-fertility (HF) and 10 low-fertility (LF) bulls, and subjected them to in vitro capacitating conditions, following which sperm viability, membrane fluidity, acrosome integrity and protein tyrosine phosphorylation were assessed using flow cytometry. We then assessed the ability of sperm to undergo hyperactivation (induced using caffeine) utilising computer-assisted sperm analysis, and the acrosome reaction (induced using calcium ionophore) using flow cytometry. When sperm were incubated in capacitating conditions, a higher percentage of viable sperm from HF bulls exhibited high membrane fluidity when compared to LF bulls (8.8 ± 0.8% and 5.8 ± 1.2%, respectively; mean ± standard error; P < 0.05). There was no difference between fertility groups in the percentage of acrosome-reacted sperm following the incubation in in vitro capacitating conditions or following the induction of the acrosome reaction using calcium ionophore. However, more sperm from HF bulls became hyperactive in response to caffeine stimulation than sperm from LF bulls (21.6 ± 2.5% versus 14.1 ± 2.4%, respectively; mean ± standard error; P < 0.05). Taken together, sperm from LF bulls had an impaired ability to undergo membrane remodulation and to hyperactivate when induced in vitro. These are key events in the journey of sperm along the female reproductive tract and in the interaction with the oocyte and thus could explain the lower field fertility exhibited by some bulls.

Identifiants

pubmed: 36332370
pii: S0093-691X(22)00429-0
doi: 10.1016/j.theriogenology.2022.10.021
pii:
doi:

Substances chimiques

Calcium Ionophores 0
Caffeine 3G6A5W338E
Tyrosine 42HK56048U

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115-121

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no competing interests.

Auteurs

Miriama Štiavnická (M)

Laboratory of Animal Reproduction, Department of Biological Sciences, Biomaterials Research Cluster, Bernal Institute, Faculty of Science and Engineering, University of Limerick, Limerick, V94 T9PX, Ireland.

Petr Hošek (P)

Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, 323 00, Czech Republic.

Laura Abril-Parreño (L)

Laboratory of Animal Reproduction, Department of Biological Sciences, Biomaterials Research Cluster, Bernal Institute, Faculty of Science and Engineering, University of Limerick, Limerick, V94 T9PX, Ireland.

David A Kenny (DA)

Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc, Meath, C15 PW93, Ireland.

Patrick Lonergan (P)

School of Agriculture and Food Science, University College Dublin, Belfield, Dublin 4, D04 V1W8, Ireland.

Sean Fair (S)

Laboratory of Animal Reproduction, Department of Biological Sciences, Biomaterials Research Cluster, Bernal Institute, Faculty of Science and Engineering, University of Limerick, Limerick, V94 T9PX, Ireland. Electronic address: Sean.Fair@ul.ie.

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