Literature DB >> 20591323

Seminal plasma proteins inhibit in vitro- and cooling-induced capacitation in boar spermatozoa.

Melissa L Vadnais1, Kenneth P Roberts.   

Abstract

Dilute boar seminal plasma (SP) has been shown to inhibit in vitro capacitation and cooling-induced capacitation-like changes in boar spermatozoa, as assessed by the ability of the spermatozoa to undergo an ionophore-induced acrosome reaction. We hypothesised that the protein component of SP is responsible for this effect. To test this hypothesis, varying concentrations of total SP protein or SP proteins fractionated by heparin binding were assayed for their ability to inhibit in vitro capacitation, as well as cooling- and cryopreservation-induced capacitation-like changes. In vitro capacitation and cooling-induced capacitation-like changes were prevented by 10% whole SP, as well as by total proteins extracted from SP at concentrations greater than 500 microg mL(-1). No amount of SP protein was able to prevent cryopreservation-induced capacitation-like changes. Total SP proteins were fractionated based on their heparin-binding properties and the heparin-binding fraction was shown to possess capacitation inhibitory activity at concentrations as low as 250 microg mL(-1). The proteins in the heparin-binding fraction were subjected to mass spectrometry and identified. The predominant proteins were three members of the spermadhesin families, namely AQN-3, AQN-1 and AWN, and SP protein pB1. We conclude that one or more of these heparin-binding SP proteins is able to inhibit in vitro capacitation and cooling-induced capacitation-like changes, but not cryopreservation-induced capacitation-like changes, in boar spermatozoa.

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Year:  2010        PMID: 20591323     DOI: 10.1071/RD09274

Source DB:  PubMed          Journal:  Reprod Fertil Dev        ISSN: 1031-3613            Impact factor:   2.311


  5 in total

1.  The Presence of Seminal Plasma during Liquid Storage of Pig Spermatozoa at 17 °C Modulates Their Ability to Elicit In Vitro Capacitation and Trigger Acrosomal Exocytosis.

Authors:  Ana Paula Pinoti Pavaneli; Sandra Recuero; Bruna Resende Chaves; Estela Garcia-Bonavila; Marc Llavanera; Elisabeth Pinart; Sergi Bonet; André Furugen Cesar De Andrade; Marc Yeste
Journal:  Int J Mol Sci       Date:  2020-06-25       Impact factor: 5.923

2.  Fractionated Seminal Plasma of Boar Ejaculates Analyzed by LC-MS/MS: Its Effects on Post-Thaw Semen Quality.

Authors:  Leyland Fraser; Karolina Wasilewska-Sakowska; Łukasz Zasiadczyk; Elżbieta Piątkowska; Krzysztof Karpiesiuk
Journal:  Genes (Basel)       Date:  2021-10-02       Impact factor: 4.096

Review 3.  Effect of Sperm Cryopreservation in Farm Animals Using Nanotechnology.

Authors:  Muhammad Faheem Akhtar; Qingshan Ma; Yan Li; Wenqiong Chai; Zhenwei Zhang; Liangliang Li; Changfa Wang
Journal:  Animals (Basel)       Date:  2022-09-02       Impact factor: 3.231

4.  Novel Flow Cytometry Analyses of Boar Sperm Viability: Can the Addition of Whole Sperm-Rich Fraction Seminal Plasma to Frozen-Thawed Boar Sperm Affect It?

Authors:  Mariana Andrade Torres; Rommy Díaz; Rodrigo Boguen; Simone Maria Massami Kitamura Martins; Gisele Mouro Ravagnani; Diego Feitosa Leal; Melissa de Lima Oliveira; Bruno Bracco Donatelli Muro; Beatriz Martins Parra; Flávio Vieira Meirelles; Frederico Ozanan Papa; José Antônio Dell'Aqua; Marco Antônio Alvarenga; Aníbal de Sant'Anna Moretti; Néstor Sepúlveda; André Furugen Cesar de Andrade
Journal:  PLoS One       Date:  2016-08-16       Impact factor: 3.240

5.  Vitrification Increased Vacuolization of Human Spematozoa: Application of MSOME Technology.

Authors:  Sara Taherzadeh; Mohammad Ali Khalili; Azam Agha-Rahimi; Fateme Anbari; Shahin Ghazali; Guido Macchiarelli
Journal:  J Reprod Infertil       Date:  2017 Apr-Jun
  5 in total

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