Proteomic Landscape of Human Sperm in Patients with Different Spermatogenic Impairments

Author:

Becker Lea Simone1ORCID,Al Smadi Mohammad A.2ORCID,Raeschle Markus3ORCID,Rishik Shusruto4,Abdul-Khaliq Hashim5,Meese Eckart1,Abu-Halima Masood15ORCID

Affiliation:

1. Institute of Human Genetics, Saarland University, 66421 Homburg, Germany

2. Reproductive Endocrinology and IVF Unit, King Hussein Medical Centre, Amman 11733, Jordan

3. Department of Molecular Genetics, TU Kaiserslautern, 67653 Kaiserslautern, Germany

4. Chair for Clinical Bioinformatics, Saarland University, 66123 Saarbrücken, Germany

5. Department of Pediatric Cardiology, Saarland University Medical Center, 66421 Homburg, Germany

Abstract

Although the proteome of sperm has been characterized, there is still a lack of high-throughput studies on dysregulated proteins in sperm from subfertile men, with only a few studies on the sperm proteome in asthenozoospermic and oligoasthenozoospermic men. Using liquid chromatography–mass spectrometry (LC-MS/MS) along with bioinformatics analyses, we investigated the proteomic landscape of sperm collected from subfertile men (n = 22), i.e., asthenozoospermic men (n = 13), oligoasthenozoospermic men (n = 9) and normozoospermic controls (n = 31). We identified 4412 proteins in human sperm. Out of these, 1336 differentially abundant proteins were identified in 70% of the samples. In subfertile men, 32 proteins showed a lower abundance level and 34 showed a higher abundance level when compared with normozoospermic men. Compared to normozoospermic controls, 95 and 8 proteins showed a lower abundance level, and 86 and 1 proteins showed a higher abundance level in asthenozoospermic and oligoasthenozoospermic men, respectively. Sperm motility and count were negatively correlated with 13 and 35 and positively correlated with 37 and 20 differentially abundant proteins in asthenozoospermic and oligoasthenozoospermic men, respectively. The combination of the proteins APCS, APOE, and FLOT1 discriminates subfertile males from normozoospermic controls with an AUC value of 0.95. Combined APOE and FN1 proteins discriminate asthenozoospermic men form controls with an AUC of 1, and combined RUVBL1 and TFKC oligoasthenozoospermic men with an AUC of 0.93. Using a proteomic approach, we revealed the proteomic landscape of sperm collected from asthenozoospermic or oligoasthenozoospermic men. Identified abundance changes of several specific proteins are likely to impact sperm function leading to subfertility. The data also provide evidence for the usefulness of specific proteins or protein combinations to support future diagnosis of male subfertility.

Funder

Hedwig-Stalter foundation

Saarland University Research Prize

Publisher

MDPI AG

Subject

General Medicine

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