Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation

Mammalian sperm must undergo a set of structural and functional changes collectively termed as capacitation to ensure a successful oocyte fertilization. However, capacitation can be compromised by cryopreservation procedures, which alter the proteome and longevity of sperm. To date, how the protein...

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Main Authors: Patricia Peris-Frau, Alicia Martín-Maestro, María Iniesta-Cuerda, Irene Sánchez-Ajofrín, Lourdes Mateos-Hernández, J. Julián Garde, Margarita Villar, Ana Josefa Soler
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/18/4596
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spelling doaj-7c1dbe0a2f014852bf9f5ae010c5c8762020-11-25T01:35:56ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-09-012018459610.3390/ijms20184596ijms20184596Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro CapacitationPatricia Peris-Frau0Alicia Martín-Maestro1María Iniesta-Cuerda2Irene Sánchez-Ajofrín3Lourdes Mateos-Hernández4J. Julián Garde5Margarita Villar6Ana Josefa Soler7SaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainSaBio IREC (CSIC-UCLM-JCCM), ETSIAM, Campus Universitario s/n, 02071 Albacete, SpainMammalian sperm must undergo a set of structural and functional changes collectively termed as capacitation to ensure a successful oocyte fertilization. However, capacitation can be compromised by cryopreservation procedures, which alter the proteome and longevity of sperm. To date, how the protein changes induced by cryopreservation could affect the acquisition of sperm fertilizing potential remains unexplored. The present study investigated the protein profile of ram sperm during in vitro capacitation before and after cryopreservation to elucidate the impact of cryopreservation on sperm capacitation at a molecular level. Fresh and cryopreserved ram sperm were incubated under capacitating (CAP) and non-capacitating (NC) conditions for 240 min. The sperm proteome of these four treatments was analyzed and compared at different incubation times using reverse phase liquid chromatography coupled to mass spectrometry (RP-LC-MS/MS). The comparison between fresh and cryopreserved sperm suggested that cryopreservation facilitated an apoptosis-stress response and redox process, while the comparison between sperm incubated in CAP and NC conditions showed that capacitation increased those biological processes associated with signaling, metabolism, motility, and reproductive processes. In addition, 14 proteins related to mitochondrial activity, sperm motility, oocyte recognition, signaling, spermatogenesis, and the apoptosis-stress response underwent significant changes in abundance over time when fresh and cryopreserved sperm incubated in CAP and NC conditions were compared. Our results indicate that disturbances in a ram sperm proteome after cryopreservation may alter the quality of sperm and its specific machinery to sustain capacitation under in vitro conditions.https://www.mdpi.com/1422-0067/20/18/4596capacitationcryopreservationproteomeram sperm
collection DOAJ
language English
format Article
sources DOAJ
author Patricia Peris-Frau
Alicia Martín-Maestro
María Iniesta-Cuerda
Irene Sánchez-Ajofrín
Lourdes Mateos-Hernández
J. Julián Garde
Margarita Villar
Ana Josefa Soler
spellingShingle Patricia Peris-Frau
Alicia Martín-Maestro
María Iniesta-Cuerda
Irene Sánchez-Ajofrín
Lourdes Mateos-Hernández
J. Julián Garde
Margarita Villar
Ana Josefa Soler
Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
International Journal of Molecular Sciences
capacitation
cryopreservation
proteome
ram sperm
author_facet Patricia Peris-Frau
Alicia Martín-Maestro
María Iniesta-Cuerda
Irene Sánchez-Ajofrín
Lourdes Mateos-Hernández
J. Julián Garde
Margarita Villar
Ana Josefa Soler
author_sort Patricia Peris-Frau
title Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
title_short Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
title_full Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
title_fullStr Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
title_full_unstemmed Freezing–Thawing Procedures Remodel the Proteome of Ram Sperm before and after In Vitro Capacitation
title_sort freezing–thawing procedures remodel the proteome of ram sperm before and after in vitro capacitation
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-09-01
description Mammalian sperm must undergo a set of structural and functional changes collectively termed as capacitation to ensure a successful oocyte fertilization. However, capacitation can be compromised by cryopreservation procedures, which alter the proteome and longevity of sperm. To date, how the protein changes induced by cryopreservation could affect the acquisition of sperm fertilizing potential remains unexplored. The present study investigated the protein profile of ram sperm during in vitro capacitation before and after cryopreservation to elucidate the impact of cryopreservation on sperm capacitation at a molecular level. Fresh and cryopreserved ram sperm were incubated under capacitating (CAP) and non-capacitating (NC) conditions for 240 min. The sperm proteome of these four treatments was analyzed and compared at different incubation times using reverse phase liquid chromatography coupled to mass spectrometry (RP-LC-MS/MS). The comparison between fresh and cryopreserved sperm suggested that cryopreservation facilitated an apoptosis-stress response and redox process, while the comparison between sperm incubated in CAP and NC conditions showed that capacitation increased those biological processes associated with signaling, metabolism, motility, and reproductive processes. In addition, 14 proteins related to mitochondrial activity, sperm motility, oocyte recognition, signaling, spermatogenesis, and the apoptosis-stress response underwent significant changes in abundance over time when fresh and cryopreserved sperm incubated in CAP and NC conditions were compared. Our results indicate that disturbances in a ram sperm proteome after cryopreservation may alter the quality of sperm and its specific machinery to sustain capacitation under in vitro conditions.
topic capacitation
cryopreservation
proteome
ram sperm
url https://www.mdpi.com/1422-0067/20/18/4596
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