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Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies
Recent studies have shown that infertility affects estimated 15% of all couples. Male infertility is the primary or contributory cause in 60% of these cases. Consequently, the application of assisted reproduction is increasing. These methods could benefit from an extended evaluation of sperm quality...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736337/ https://www.ncbi.nlm.nih.gov/pubmed/25926605 http://dx.doi.org/10.4103/1008-682X.151400 |
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author | Capkova, Jana Kubatova, Alena Ded, Lukas Tepla, Olina Peknicova, Jana |
author_facet | Capkova, Jana Kubatova, Alena Ded, Lukas Tepla, Olina Peknicova, Jana |
author_sort | Capkova, Jana |
collection | PubMed |
description | Recent studies have shown that infertility affects estimated 15% of all couples. Male infertility is the primary or contributory cause in 60% of these cases. Consequently, the application of assisted reproduction is increasing. These methods could benefit from an extended evaluation of sperm quality. For this reason, we analyzed sperm proteins from 30 men with normal spermiograms and 30 men with asthenozoospermia. Ejaculates of both groups were tested by flow cytometry (FCM) and fluorescence with a set of well-characterized anti-human sperm Hs-monoclonal antibodies (MoAbs), which were generated in our laboratory. No statistically significant differences were found between normospermics and asthenospermics in the expression of the sperm surface protein clusterin, evaluated with Hs-3 MoAb, and semenogelin, evaluated with Hs-9 MoAb. However, FCM revealed quantitative differences in the acrosomal proteins between normozoospermic and asthenozoospermic men, namely, in glyceraldehyde-3-phosphate dehydrogenase, evaluated with Hs-8 MoAb, valosin-containing protein, evaluated with Hs-14 MoAb, and ATP synthase (cAMP-dependent protein kinase II, PRKAR2A), evaluated with MoAb Hs-36. Asthenozoospermic men displayed a highly reduced expression of intra-acrosomal proteins, with a likely decrease in sperm quality, and thus a negative impact on successful reproduction. Asthenozoospermia seems to be a complex disorder involving intra-acrosomal proteins. |
format | Online Article Text |
id | pubmed-4736337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47363372016-02-04 Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies Capkova, Jana Kubatova, Alena Ded, Lukas Tepla, Olina Peknicova, Jana Asian J Androl Original Article Recent studies have shown that infertility affects estimated 15% of all couples. Male infertility is the primary or contributory cause in 60% of these cases. Consequently, the application of assisted reproduction is increasing. These methods could benefit from an extended evaluation of sperm quality. For this reason, we analyzed sperm proteins from 30 men with normal spermiograms and 30 men with asthenozoospermia. Ejaculates of both groups were tested by flow cytometry (FCM) and fluorescence with a set of well-characterized anti-human sperm Hs-monoclonal antibodies (MoAbs), which were generated in our laboratory. No statistically significant differences were found between normospermics and asthenospermics in the expression of the sperm surface protein clusterin, evaluated with Hs-3 MoAb, and semenogelin, evaluated with Hs-9 MoAb. However, FCM revealed quantitative differences in the acrosomal proteins between normozoospermic and asthenozoospermic men, namely, in glyceraldehyde-3-phosphate dehydrogenase, evaluated with Hs-8 MoAb, valosin-containing protein, evaluated with Hs-14 MoAb, and ATP synthase (cAMP-dependent protein kinase II, PRKAR2A), evaluated with MoAb Hs-36. Asthenozoospermic men displayed a highly reduced expression of intra-acrosomal proteins, with a likely decrease in sperm quality, and thus a negative impact on successful reproduction. Asthenozoospermia seems to be a complex disorder involving intra-acrosomal proteins. Medknow Publications & Media Pvt Ltd 2016 2015-04-28 /pmc/articles/PMC4736337/ /pubmed/25926605 http://dx.doi.org/10.4103/1008-682X.151400 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Capkova, Jana Kubatova, Alena Ded, Lukas Tepla, Olina Peknicova, Jana Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title | Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title_full | Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title_fullStr | Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title_full_unstemmed | Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title_short | Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
title_sort | evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736337/ https://www.ncbi.nlm.nih.gov/pubmed/25926605 http://dx.doi.org/10.4103/1008-682X.151400 |
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