Validation of merocyanine 540 staining as a technique for assessing capacitation-related membrane destabilization of fresh dog sperm

dc.contributor.authorSteckler, Daniela
dc.contributor.authorStout, T.A.E. (Tom)
dc.contributor.authorDurandt, Chrisna
dc.contributor.authorNothling, Johan Oliviette
dc.date.accessioned2015-06-19T08:50:03Z
dc.date.available2015-06-19T08:50:03Z
dc.date.issued2015-06
dc.description.abstractThe aim of this study was to determine whether flow cytometric evaluation of combined merocyanine 540 and Yo-Pro 1 (M540-YP) staining would identify viable dog sperm that had undergone membrane stabilization known to be associated with capacitation in other species, and whether such destabilization is detected earlier than when using the tyrosine phosphorylation and ethidium homodimer (TP-EH) stain combination with epifluorescence microscopy. Semen from nine dogs was collected and incubated in parallel in bicarbonate-free modified Tyrode’s medium ( BIC), medium containing 15 mM bicarbonate (þBIC), dog prostatic fluid, and in PBS. Aliquots for staining were removed at various time points during incubation of up to 6 hours. Staining with M540-YP allowed the classification of dog sperm as viable without destabilized membranes, viable with destabilized membranes, nonviable without destabilized membranes, or nonviable with destabilized membranes. The percentage of viable sperm detected using EH (83.5 1.37%; mean SEM) was higher than when using YP (66.7 1.37%: P < 0.05; n ¼ 54 semen samples). On the other hand, M540-YP identified a higher percentage of viable sperm with destabilized membranes than TP-EH (75 1.76% vs. 35 1.70%: P < 0.05; n ¼ 54 semen samples). Staining with M540-YP indicated a rapid increase in the percentage of viable sperm with destabilized membranes, reaching a maximum during the first 30 minutes of incubation in þBIC. For all other treatments (i.e., BIC, prostatic fluid, and PBS), the peak in the percentage of viable sperm with destabilized membranes was reached as much as 90 to 210 minutes later than incubation in þBIC. The lowest percentage of viable sperm showing signs of capacitation was recorded during incubation in PBS. We conclude that YP identifies sperm committed to cell death earlier than EH, and that the M540-YP stain combination identifies membrane destabilization known to be associated with capacitation in other species earlier than the TP-EH stain combination.en_ZA
dc.description.embargo2016-06-30en_ZA
dc.description.librarianhb2015en_ZA
dc.description.sponsorshipNational Research Foundation, South Africaen_ZA
dc.description.urihttp://www.theriojournal.com/en_ZA
dc.identifier.citationSteckler, D, Stout, TAE, Durandt, C & Nothling, JO 2015, 'Validation of merocyanine 540 staining as a technique for assessing capacitation-related membrane destabilization of fresh dog sperm', Theriogenology, vol. 83, no. 9, pp. 1451-1460.en_ZA
dc.identifier.issn0093-691X (print)
dc.identifier.issn1879-3231 (online)
dc.identifier.other10.1016/j.theriogenology.2015.01.019
dc.identifier.otherO-6382-2014
dc.identifier.other6602528464
dc.identifier.urihttp://hdl.handle.net/2263/45613
dc.language.isoenen_ZA
dc.publisherElsevieren_ZA
dc.relation.requiresAdobe Acrobat Readeren
dc.rights© 2015 Elsevier Inc. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Theriogenology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Theriogenology, vol. 83, no. 9, pp. 1451-1460, 2015. doi :10.1016/j.theriogenology.2015.01.019en_ZA
dc.subjectDogsen_ZA
dc.subjectEthidium homodimeren_ZA
dc.subjectTyrosine phosphorylationen_ZA
dc.subjectYo-Pro 1en_ZA
dc.subjectCapacitationen_ZA
dc.subjectMembrane destabilizationen_ZA
dc.subjectSemenen_ZA
dc.titleValidation of merocyanine 540 staining as a technique for assessing capacitation-related membrane destabilization of fresh dog spermen_ZA
dc.typePostprint Articleen_ZA

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