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Proteomic analysis of seminal fluid from men exhibiting oxidative stress

BACKGROUND: Seminal plasma serves as a natural reservoir of antioxidants. It helps to remove excessive formation of reactive oxygen species (ROS) and consequently, reduce oxidative stress. Proteomic profiling of seminal plasma proteins is important to understand the molecular mechanisms underlying o...

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Autores principales: Sharma, Rakesh, Agarwal, Ashok, Mohanty, Gayatri, Du Plessis, Stefan S, Gopalan, Banu, Willard, Belinda, Yadav, Satya P, Sabanegh, Edmund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846593/
https://www.ncbi.nlm.nih.gov/pubmed/24004880
http://dx.doi.org/10.1186/1477-7827-11-85
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author Sharma, Rakesh
Agarwal, Ashok
Mohanty, Gayatri
Du Plessis, Stefan S
Gopalan, Banu
Willard, Belinda
Yadav, Satya P
Sabanegh, Edmund
author_facet Sharma, Rakesh
Agarwal, Ashok
Mohanty, Gayatri
Du Plessis, Stefan S
Gopalan, Banu
Willard, Belinda
Yadav, Satya P
Sabanegh, Edmund
author_sort Sharma, Rakesh
collection PubMed
description BACKGROUND: Seminal plasma serves as a natural reservoir of antioxidants. It helps to remove excessive formation of reactive oxygen species (ROS) and consequently, reduce oxidative stress. Proteomic profiling of seminal plasma proteins is important to understand the molecular mechanisms underlying oxidative stress and sperm dysfunction in infertile men. METHODS: This prospective study consisted of 52 subjects: 32 infertile men and 20 healthy donors. Once semen and oxidative stress parameters were assessed (ROS, antioxidant concentration and DNA damage), the subjects were categorized into ROS positive (ROS+) or ROS negative (ROS-). Seminal plasma from each group was pooled and subjected to proteomics analysis. In-solution digestion and protein identification with liquid chromatography tandem mass spectrometry (LC-MS/MS), followed by bioinformatics analyses was used to identify and characterize potential biomarker proteins. RESULTS: A total of 14 proteins were identified in this analysis with 7 of these common and unique proteins were identified in both the ROS+ and ROS- groups through MASCOT and SEQUEST analyses, respectively. Prolactin-induced protein was found to be more abundantly present in men with increased levels of ROS. Gene ontology annotations showed extracellular distribution of proteins with a major role in antioxidative activity and regulatory processes. CONCLUSIONS: We have identified proteins that help protect against oxidative stress and are uniquely present in the seminal plasma of the ROS- men. Men exhibiting high levels of ROS in their seminal ejaculate are likely to exhibit proteins that are either downregulated or oxidatively modified, and these could potentially contribute to male infertility.
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spelling pubmed-38465932013-12-03 Proteomic analysis of seminal fluid from men exhibiting oxidative stress Sharma, Rakesh Agarwal, Ashok Mohanty, Gayatri Du Plessis, Stefan S Gopalan, Banu Willard, Belinda Yadav, Satya P Sabanegh, Edmund Reprod Biol Endocrinol Research BACKGROUND: Seminal plasma serves as a natural reservoir of antioxidants. It helps to remove excessive formation of reactive oxygen species (ROS) and consequently, reduce oxidative stress. Proteomic profiling of seminal plasma proteins is important to understand the molecular mechanisms underlying oxidative stress and sperm dysfunction in infertile men. METHODS: This prospective study consisted of 52 subjects: 32 infertile men and 20 healthy donors. Once semen and oxidative stress parameters were assessed (ROS, antioxidant concentration and DNA damage), the subjects were categorized into ROS positive (ROS+) or ROS negative (ROS-). Seminal plasma from each group was pooled and subjected to proteomics analysis. In-solution digestion and protein identification with liquid chromatography tandem mass spectrometry (LC-MS/MS), followed by bioinformatics analyses was used to identify and characterize potential biomarker proteins. RESULTS: A total of 14 proteins were identified in this analysis with 7 of these common and unique proteins were identified in both the ROS+ and ROS- groups through MASCOT and SEQUEST analyses, respectively. Prolactin-induced protein was found to be more abundantly present in men with increased levels of ROS. Gene ontology annotations showed extracellular distribution of proteins with a major role in antioxidative activity and regulatory processes. CONCLUSIONS: We have identified proteins that help protect against oxidative stress and are uniquely present in the seminal plasma of the ROS- men. Men exhibiting high levels of ROS in their seminal ejaculate are likely to exhibit proteins that are either downregulated or oxidatively modified, and these could potentially contribute to male infertility. BioMed Central 2013-09-03 /pmc/articles/PMC3846593/ /pubmed/24004880 http://dx.doi.org/10.1186/1477-7827-11-85 Text en Copyright © 2013 Sharma et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Sharma, Rakesh
Agarwal, Ashok
Mohanty, Gayatri
Du Plessis, Stefan S
Gopalan, Banu
Willard, Belinda
Yadav, Satya P
Sabanegh, Edmund
Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title_full Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title_fullStr Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title_full_unstemmed Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title_short Proteomic analysis of seminal fluid from men exhibiting oxidative stress
title_sort proteomic analysis of seminal fluid from men exhibiting oxidative stress
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846593/
https://www.ncbi.nlm.nih.gov/pubmed/24004880
http://dx.doi.org/10.1186/1477-7827-11-85
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