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Identification of the SP22 Sperm Protein in Santa Ines and Dorper Rams

dc.contributor.authorFavareto, A. P. A. [UNESP]
dc.contributor.authorRodello, L. [UNESP]
dc.contributor.authorTaconeli, C. A. [UNESP]
dc.contributor.authorBicudo, Sony Dimas [UNESP]
dc.contributor.authorKlinefelter, G. R. [UNESP]
dc.contributor.authorKempinas, W. G. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2013-09-30T18:39:25Z
dc.date.accessioned2014-05-20T13:41:48Z
dc.date.available2013-09-30T18:39:25Z
dc.date.available2014-05-20T13:41:48Z
dc.date.issued2010-04-01
dc.description.abstractContentsThe sperm membrane protein referred to as SP22 has been identified in different species and, at least in rats, is highly correlated with fertility. The goals of this study were to identify and to quantify the SP22 protein on spermatozoa from adult rams (Dorper and Santa Ines breeds), and to correlate its levels to morphological and kinematics parameters. SP22 on ram sperm was effectively quantified by both enzyme-linked immunosorbent assay (ELISA) and fluorescein isothiocyanate immunostaining analysis and the two methods were significantly correlated (R2 = 0.70). Clustering analysis of motility parameters obtained by computer-assisted semen analysis system was used to establish that three distinct kinematic subpopulations with different vigour and progressiveness coexistent within ejaculate. While there were significant differences in the distribution of the three subpopulations in the rams, there was no significant correlation between the proportion of each subpopulation in the rams and the SP22 levels. Quantification of SP22 immunostaining intensity was not correlated with any of the sperm parameters. However, SP22 levels obtained by ELISA were negatively correlated with morphological abnormalities and positively correlated with membrane integrity (three variable R2 = 0.47). Future breeding studies are now needed to validate that this protein is a biomarker of fertility in this species.en
dc.description.affiliationUNESP, Inst Biociencias, Dept Morfol, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Biociencias, Dept Morfol, BR-18618000 Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 06/54103-1
dc.description.sponsorshipIdCNPq: 501306/2005-6
dc.format.extent323-330
dc.identifierhttp://dx.doi.org/10.1111/j.1439-0531.2008.01313.x
dc.identifier.citationReproduction In Domestic Animals. Malden: Wiley-blackwell Publishing, Inc, v. 45, n. 2, p. 323-330, 2010.
dc.identifier.doi10.1111/j.1439-0531.2008.01313.x
dc.identifier.issn0936-6768
dc.identifier.lattes6326450271169741
dc.identifier.urihttp://hdl.handle.net/11449/14509
dc.identifier.wosWOS:000275731900021
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing, Inc
dc.relation.ispartofReproduction in Domestic Animals
dc.relation.ispartofjcr1.422
dc.relation.ispartofsjr0,594
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleIdentification of the SP22 Sperm Protein in Santa Ines and Dorper Ramsen
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-blackwell Publishing, Inc
dspace.entity.typePublication
unesp.author.lattes6326450271169741
unesp.author.orcid0000-0002-2112-5123[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentMorfologia - IBBpt

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