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Male infertility and Perfluoroalkyl and poly-fluoroalkyl substances: Evidence for alterations in phosphorylation of proteins and fertility-related functional attributes in bull spermatozoa.
Kumaresan, Arumugam; Yadav, Pankaj; Sinha, Manish Kumar; Nag, Pradeep; John Peter, Ebenezer Samuel King; Mishra, Jay S; Kumar, Sathish.
Affiliation
  • Kumaresan A; Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
  • Yadav P; Theriogenology Laboratory, Southern Regional Station of ICAR National Dairy Research Institute, Bengaluru 560030, Karnataka, India.
  • Sinha MK; Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
  • Nag P; Theriogenology Laboratory, Southern Regional Station of ICAR National Dairy Research Institute, Bengaluru 560030, Karnataka, India.
  • John Peter ESK; Department of Animal Sciences, University of Missouri, Columbia 65211, USA.
  • Mishra JS; Theriogenology Laboratory, Southern Regional Station of ICAR National Dairy Research Institute, Bengaluru 560030, Karnataka, India.
  • Kumar S; Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI 53706, USA.
Biol Reprod ; 2024 Jun 07.
Article de En | MEDLINE | ID: mdl-38847481
ABSTRACT

BACKGROUND:

Perfluoroalkyl and poly-fluoroalkyl substances (PFAS) are pervasive environmental pollutants and emerging risk factors for reproductive health. Although epidemiological evidence supports the link between these substances and male infertility, their specific effects on male fertility remain poorly understood.

OBJECTIVES:

Investigate the effect of perfluorooctane sulfonic acid (PFOS), the most prevalent and prominent PFAS, on bull sperm protein phosphorylation, a post-translational modification process governing sperm functionality and fertility.

METHODS:

We exposed bull sperm to PFOS at 10 µM (average population level) and 100 µM (high-exposure level), and analyzed global proteome and phosphoproteome profile by TMT labeling and NanoLC-MS/MS. We also measured sperm fertility functions by flow cytometry.

RESULTS:

PFOS at 10 µM altered sperm proteins linked to spermatogenesis and chromatin condensation, while at 100 µM, PFOS affected proteins associated with motility and fertility. We detected 299 phosphopeptides from 116 proteins, with 45 exhibiting differential expression between control and PFOS groups. PFOS dysregulated phosphorylation of key proteins (ACRBP, PRKAR2A, RAB2B, SPAG8, TUBB4B, ZPBP, and C2CD6) involved in sperm capacitation, acrosome reaction, sperm-egg interaction, and fertilization. PFOS also affected phosphorylation of other proteins (AQP7, HSBP9, IL4I1, PRKAR1A, and CCT8L2) related to sperm stress resistance and cryotolerance. Notably, 4 proteins (PRM1, ACRBP, TSSK1B, and CFAP45) exhibited differential regulation at both the proteomic and phosphoproteomic levels. Flow cytometric analysis confirmed that PFOS increased protein phosphorylation in sperm as well as reduced sperm motility, viability, calcium, and membrane potential and increased mitochondrial ROS in a dose-dependent manner.

CONCLUSIONS:

This study shows that PFOS exposure adversely impacts phosphorylation of proteins critical for bull sperm function and fertilization. Moreover, the concentration of PFOS influences the severity of these effects. The comprehensive bull sperm phosphoproteomics data from this study can help us understand the molecular mechanisms of environmental exposure-related male infertility.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Biol Reprod Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Biol Reprod Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique