Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.

Cellular membranes are heterogeneous, and this has a great impact on cellular function. Despite the central role of membrane functions in multiple cellular processes in sperm, their molecular mechanisms are poorly understood. Membrane rafts are specific membrane domains enriched in cholesterol, gang...

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Main Authors: Ai Ushiyama, Atsushi Tajima, Naoto Ishikawa, Atsushi Asano
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5667776?pdf=render
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spelling doaj-4312a319a1e444da9412746971f622762020-11-24T21:30:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011211e018648210.1371/journal.pone.0186482Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.Ai UshiyamaAtsushi TajimaNaoto IshikawaAtsushi AsanoCellular membranes are heterogeneous, and this has a great impact on cellular function. Despite the central role of membrane functions in multiple cellular processes in sperm, their molecular mechanisms are poorly understood. Membrane rafts are specific membrane domains enriched in cholesterol, ganglioside GM1, and functional proteins, and they are involved in the regulation of a variety of cellular functions. Studies of the functional characterization of membrane rafts in mammalian sperm have demonstrated roles in sperm-egg binding and the acrosomal reaction. Recently, our biochemical and cell biological studies showed that membrane rafts are present and might play functional roles in chicken sperm. In this study, we isolated membrane rafts from chicken sperm as a detergent-resistant membranes (DRM) floating on a density gradient in the presence of 1% Triton X-100, and characterized the function and proteomes associated with these domains. Biochemical comparison of the DRM between fresh and cryopreserved sperm demonstrated that cryopreservation induces cholesterol loss specifically from membrane rafts, indicating the functional connection with reduced post-thaw fertility in chicken sperm. Furthermore, using an avidin-biotin system, we found that sperm DRM is highly enriched in a 60 KDa single protein able to bind to the inner perivitelline layer. To identify possible roles of membrane rafts, quantitative proteomics, combined with a stable isotope dimethyl labeling approach, identified 82 proteins exclusively or relatively more associated with membrane rafts. Our results demonstrate the functional distinctions between membrane domains and provide compelling evidence that membrane rafts are involved in various cellular pathways inherent to chicken sperm.http://europepmc.org/articles/PMC5667776?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ai Ushiyama
Atsushi Tajima
Naoto Ishikawa
Atsushi Asano
spellingShingle Ai Ushiyama
Atsushi Tajima
Naoto Ishikawa
Atsushi Asano
Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
PLoS ONE
author_facet Ai Ushiyama
Atsushi Tajima
Naoto Ishikawa
Atsushi Asano
author_sort Ai Ushiyama
title Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
title_short Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
title_full Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
title_fullStr Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
title_full_unstemmed Characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
title_sort characterization of the functions and proteomes associated with membrane rafts in chicken sperm.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Cellular membranes are heterogeneous, and this has a great impact on cellular function. Despite the central role of membrane functions in multiple cellular processes in sperm, their molecular mechanisms are poorly understood. Membrane rafts are specific membrane domains enriched in cholesterol, ganglioside GM1, and functional proteins, and they are involved in the regulation of a variety of cellular functions. Studies of the functional characterization of membrane rafts in mammalian sperm have demonstrated roles in sperm-egg binding and the acrosomal reaction. Recently, our biochemical and cell biological studies showed that membrane rafts are present and might play functional roles in chicken sperm. In this study, we isolated membrane rafts from chicken sperm as a detergent-resistant membranes (DRM) floating on a density gradient in the presence of 1% Triton X-100, and characterized the function and proteomes associated with these domains. Biochemical comparison of the DRM between fresh and cryopreserved sperm demonstrated that cryopreservation induces cholesterol loss specifically from membrane rafts, indicating the functional connection with reduced post-thaw fertility in chicken sperm. Furthermore, using an avidin-biotin system, we found that sperm DRM is highly enriched in a 60 KDa single protein able to bind to the inner perivitelline layer. To identify possible roles of membrane rafts, quantitative proteomics, combined with a stable isotope dimethyl labeling approach, identified 82 proteins exclusively or relatively more associated with membrane rafts. Our results demonstrate the functional distinctions between membrane domains and provide compelling evidence that membrane rafts are involved in various cellular pathways inherent to chicken sperm.
url http://europepmc.org/articles/PMC5667776?pdf=render
work_keys_str_mv AT aiushiyama characterizationofthefunctionsandproteomesassociatedwithmembraneraftsinchickensperm
AT atsushitajima characterizationofthefunctionsandproteomesassociatedwithmembraneraftsinchickensperm
AT naotoishikawa characterizationofthefunctionsandproteomesassociatedwithmembraneraftsinchickensperm
AT atsushiasano characterizationofthefunctionsandproteomesassociatedwithmembraneraftsinchickensperm
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