Clusterin expression and distribution in spermatozoa as predictor of male fertility

Author:

Hernández‐Herrador María1,Marilina García‐Aranda2345,Luisa Hortas María6,Carrillo‐Lucena Silvia1,Caracuel Zaira2,Castilla‐Alcalá José Antonio78,Martín‐García Desirée2345,Redondo Maximino23459

Affiliation:

1. Reproduction Unit Hospital Universitario Costa del Sol Marbella Spain

2. Research and Innovation Unit Hospital Universitario Costa del Sol Marbella Spain

3. Surgical Specialties, Biochemistry, Molecular Biology and Immunology Department, Faculty of Medicine Malaga University Malaga Spain

4. Instituto de Investigación Biomédica de Málaga (IBIMA)‐Plataforma Bionand Research Institute Malaga Spain

5. Research Network on Chronicity, Primary Care and Health Promotion (RICAPPS)

6. Clinical Laboratories Area Hospital Universitario Costa del Sol Marbella Spain

7. Reproduction Unit (Clinical Laboratory and Obstetrics and Gynecology Clinical Management Units) Hospital Universitario Virgen de las Nieves Granada Spain

8. Instituto de Investigación Biosanitaria (ibs.GRANADA) Research Institute Universidad de Granada Granada Spain

9. REDISSEC (Health Research on Chronic Patients Network)

Abstract

AbstractClusterin (CLU), one of the main glycoproteins in mammalian semen and the male reproductive tract, plays a role in spermatogenesis and sperm maturation. Given the poor reliability of classic seminal studies in determining male‐fertilizing capacity and the differences in CLU abundance between normal and abnormal spermatozoa, we investigated the potential value of mRNA‐CLU levels and protein distribution in spermatozoa as markers of sperm quality and predictors of male fertility. This multicenter study included 90 patients undergoing in vitro fertilization (IVF) treatment with their partners, and a control group of 36 fertile males with normal seminograms. We assessed the relationship between IVF treatment outcomes, seminogram variables, mRNA‐CLU levels by quantitative real‐time‐PCR and CLU distribution by immunostaining in spermatozoa. Our study reveals CLU staining in the acrosome (p = 0.002, OR 14.8, 95% CI: 2.7–79.3) and mRNA‐CLU levels (p = 0.005, OR 10.85, 95% CI: 2.0–57.4) as independent risk factors for pregnancy failure, irrespective of traditional seminogram variables. Additionally, our results suggest that CLU, and specially its secreted isoform, constitutes a component of the protein pool that human spermatozoa can produce during its maturation process, exhibiting a variable abundance and distribution in spermatozoa from fertile men compared to those in patients with altered seminograms and infertile patients with normal seminograms. Our study is the first to identify mRNA‐CLU levels and CLU immunostaining in the spermatozoa acrosome as independent risk factors for pregnancy failure, with distribution patterns correlating with sperm maturity and seminogram alterations.

Publisher

Wiley

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