| Literature DB >> 31848259 |
Jacob Netherton1, Rachel A Ogle1, Louise Hetherington1, Ana Izabel Silva Balbin Villaverde2, Hubert Hondermarck3, Mark A Baker4.
Abstract
Male infertility is widespread and estimated to affect 1 in 20 men. Although in some cases the etiology of the condition is well understood, for at least 50% of men, the underlying cause is yet to be classified. Male infertility, or subfertility, is often diagnosed by looking at total sperm produced, motility of the cells and overall morphology. Although counting spermatozoa and their associated motility is routine, morphology assessment is highly subjective, mainly because of the procedure being based on microscopic examination. A failure to diagnose male-infertility or sub-fertility has led to a situation where assisted conception is often used unnecessarily. As such, biomarkers of male infertility are needed to help establish a more consistent diagnosis. In the present study, we compared nuclear extracts from both high- and low-quality spermatozoa by LC-MS/MS based proteomic analysis. Our data shows that nuclear retention of specific proteins is a common facet among low-quality sperm cells. We demonstrate that the presence of Topoisomerase 2A in the sperm head is highly correlated to poor head morphology. Topoisomerase 2A is therefore a potential new biomarker for confirming male infertility in clinical practice.Entities:
Keywords: SWATH-MS; biomarker: prognostic; cell fractionation; male fertility; mass spectrometry; nucleus; spermatozooa; subcellular analysis
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Year: 2019 PMID: 31848259 PMCID: PMC7050105 DOI: 10.1074/mcp.RA119.001626
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911