GSTM3, but not IZUMO1, is a cryotolerance marker of boar sperm
dc.contributor.author
dc.date.accessioned
2020-06-19T06:28:09Z
dc.date.available
2020-06-19T06:28:09Z
dc.date.issued
2019-08-15
dc.identifier.uri
dc.description.abstract
Cryopreservation is currently the most efficient method for long-term preservation of mammalian
gametes and is extensively used in swine artificial insemination (AI) centres. However, it is well-known that
cryopreservation procedures induce changes in the water phase in both intra and extracellular compartments,
which alter the content and localisation of several proteins and ends up curtailing the structural integrity of
functional sperm (i.e., cryoinjuries). Alterations and deficiencies of sperm-oocyte binding proteins during gamete
recognition are one of the causes of reproductive failure both in vitro and in vivo. In this sense, characterisation of
cryopreservation effects upon oocyte-binding proteins of sperm, such as IZUMO1 and GSTM3, is essential when
assessing the impact of this technique in swine reproduction.
Results: Cryopreservation was found to induce changes in the localisation of IZUMO1 and GSTM3 in boar sperm.
However, the relative content of both proteins was not altered after thawing. Furthermore, whereas IZUMO1
content was found not to be related to the cryotolerance of boar sperm, GSTM3 content was observed to be
higher in poor (PFE) than in good (GFE) freezability ejaculates in both pre-frozen (1.00 INT·mm2 ± 0.14 INT·mm2 vs.
0.72 INT·mm2 ± 0.15 INT·mm2
; P < 0.05) and post-thawed (0.96 INT·mm2 ± 0.20 INT·mm2 vs. 70 INT·mm2 ± 0.19
INT·mm2
; P < 0.05) samples. Moreover, GSTM3 levels were found to be higher in those spermatozoa that exhibited
low mitochondrial activity, high reactive oxygen species (ROS) production, and high membrane lipid disorder postthaw (P < 0.05).
Conclusions: The difference in GSTM3 content between GFE and PFE, together with this protein having been found
to be related to poor sperm quality post-thaw, suggests that it could be used as a cryotolerance marker of boar
spermatozoa. Furthermore, both IZUMO1 and GSTM3 relocate during cryopreservation, which could contribute to the
reduced fertilising capacity of frozen-thawed boar sperm
dc.description.sponsorship
The authors acknowledge the support from Ministry of Science, Innovation
and Universities, Spain (Grants: RYC-2014-15581, AGL2017–88329-R and FJCI2017-31689) and European Commission (H2020-MSCA-IF-79212)
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
BMC
dc.relation.isformatof
Reproducció digital del document publicat a: https://doi.org/10.1186/s40104-019-0370-5
dc.relation.ispartof
Journal of Animal Science and Biotechnology, 2019, vol. 10, p. 61
dc.relation.ispartofseries
Articles publicats (D-B)
dc.rights
Attribution 4.0 International
dc.rights.uri
dc.subject
dc.title
GSTM3, but not IZUMO1, is a cryotolerance marker of boar sperm
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.relation.projectID
info:eu-repo/grantAgreement/MINECO//RYC-2014-15581/ES/RYC-2014-15581/
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/AGL2017-88329-R/ES/MEJORA DEL RENDIMIENTO REPRODUCTIVO DEL SEMEN REFRIGERADO Y CONGELADO/DESCONGELADO DE PORCINO Y BOVINO MEDIANTE EL USO DE LA FOTOESTIMULACION/
dc.type.version
info:eu-repo/semantics/publishedVersion
dc.identifier.doi
dc.identifier.idgrec
029943
dc.contributor.funder
dc.type.peerreviewed
peer-reviewed
dc.relation.FundingProgramme
dc.relation.ProjectAcronym
dc.identifier.eissn
2049-1891