Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients
Purpose: Seminal plasma provides a nutritive and protective milieu for spermatozoa. It contains factors/proteins required for sperm maturation, hyperactivation, capacitation and acrosome reaction. Alteration in the expression levels of seminal plasma proteins affect the fertilization process. The...
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doaj-8749db5b98334f4686ea725a3371fa072020-12-22T05:22:37ZengKorean Society for Sexual Medicine and AndrologyThe World Journal of Men's Health2287-42082287-46902021-01-01391909810.5534/wjmh.180118Proteomic Profiling of Seminal Plasma Proteins in Varicocele PatientsManesh Kumar Panner Selvam0https://orcid.org/0000-0002-9120-2278Ashok Agarwal1https://orcid.org/0000-0003-0585-1026Cleveland ClinicCleveland ClinicPurpose: Seminal plasma provides a nutritive and protective milieu for spermatozoa. It contains factors/proteins required for sperm maturation, hyperactivation, capacitation and acrosome reaction. Alteration in the expression levels of seminal plasma proteins affect the fertilization process. The main objective of this study is to compare the seminal plasma proteome of healthy fertile men (control group) with varicocele patients in order to identify the differentially expressed seminal plasma proteins. Materials and Methods: Pooled seminal plasma samples from control (n=5) and varicocele (unilateral: n=5 and bilateral: n=5) subjects were used for proteomic profiling and functional bioinformatic analysis. Key differentially expressed proteins (DEPs) associated with binding of zona pellucida (acrosin; ACR), protein folding (heat shock related 70 kDa protein 2; HSPA2), oxidative stress (peroxiredoxin 2; PRDX2), lipid peroxidation and DNA fragmentation (apolipoprotein A2; APOA2) were validated by Western blot. Statistical analysis was conducted using Mann–Whitney test. Results: A total of 412 and 486 proteins were detected in seminal plasma of control group and varicocele patients respectively. Twenty-eight proteins were identified as DEPs between varicocele and control group. Validation of DEPs revealed downregulation of HSPA2 (p=0.0037) as well as APOA2 (p=0.0373), and upregulation of PRDX2 (p=0.0474). Conclusions: The seminal plasma protein profile of varicocele patients differ from healthy fertile men. Aberrant expression of seminal plasma proteins serve as an indicator of sperm pathology in varicocele patients.infertilitymaleproteomicsseminal plasmavaricocele |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Manesh Kumar Panner Selvam Ashok Agarwal |
spellingShingle |
Manesh Kumar Panner Selvam Ashok Agarwal Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients The World Journal of Men's Health infertility male proteomics seminal plasma varicocele |
author_facet |
Manesh Kumar Panner Selvam Ashok Agarwal |
author_sort |
Manesh Kumar Panner Selvam |
title |
Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients |
title_short |
Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients |
title_full |
Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients |
title_fullStr |
Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients |
title_full_unstemmed |
Proteomic Profiling of Seminal Plasma Proteins in Varicocele Patients |
title_sort |
proteomic profiling of seminal plasma proteins in varicocele patients |
publisher |
Korean Society for Sexual Medicine and Andrology |
series |
The World Journal of Men's Health |
issn |
2287-4208 2287-4690 |
publishDate |
2021-01-01 |
description |
Purpose: Seminal plasma provides a nutritive and protective milieu for spermatozoa. It contains factors/proteins required
for sperm maturation, hyperactivation, capacitation and acrosome reaction. Alteration in the expression levels of seminal
plasma proteins affect the fertilization process. The main objective of this study is to compare the seminal plasma proteome
of healthy fertile men (control group) with varicocele patients in order to identify the differentially expressed seminal plasma
proteins.
Materials and Methods: Pooled seminal plasma samples from control (n=5) and varicocele (unilateral: n=5 and bilateral: n=5)
subjects were used for proteomic profiling and functional bioinformatic analysis. Key differentially expressed proteins (DEPs)
associated with binding of zona pellucida (acrosin; ACR), protein folding (heat shock related 70 kDa protein 2; HSPA2),
oxidative stress (peroxiredoxin 2; PRDX2), lipid peroxidation and DNA fragmentation (apolipoprotein A2; APOA2) were validated
by Western blot. Statistical analysis was conducted using Mann–Whitney test.
Results: A total of 412 and 486 proteins were detected in seminal plasma of control group and varicocele patients respectively.
Twenty-eight proteins were identified as DEPs between varicocele and control group. Validation of DEPs revealed downregulation
of HSPA2 (p=0.0037) as well as APOA2 (p=0.0373), and upregulation of PRDX2 (p=0.0474).
Conclusions: The seminal plasma protein profile of varicocele patients differ from healthy fertile men. Aberrant expression of
seminal plasma proteins serve as an indicator of sperm pathology in varicocele patients. |
topic |
infertility male proteomics seminal plasma varicocele |
work_keys_str_mv |
AT maneshkumarpannerselvam proteomicprofilingofseminalplasmaproteinsinvaricocelepatients AT ashokagarwal proteomicprofilingofseminalplasmaproteinsinvaricocelepatients |
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