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Theriogenology · 2026

Seminal extracellular vesicles improve cryosurvival and fertility potential of kundhi buffalo sperm.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
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Malak Kashif Ali, Korejo Nazar Ali, Lund Arab Khan, Malak Atif Ali, Magsi Abdul Samad, Bux Rasool, Aqeel Muhammad

Аннотация

Buffaloes are important contributors to agricultural production in many developing countries, yet poor semen cryosurvival remains a major challenge for efficient artificial insemination and genetic improvement. In recent years, small extracellular vesicles (sEVs) have emerged as important mediators of intercellular communication and reproductive function; however, their potential as supplements for improving buffalo semen cryosurvival remains poorly understood. Therefore, this study evaluated the influence of adding a seminal plasma-derived small extracellular vesicle-enriched preparation to a Tris extender using post-thaw sperm traits, oxidative status, DNA integrity, HSP70 and PRM1 transcript abundance, and fertility of Kundhi buffalo bull semen. Seminal plasma-derived particles were isolated and characterized by nanoparticle tracking analysis, showing a mean diameter of 117.8 ± 2.47 nm, modal diameter of 89.4 ± 1.41 nm, and concentration of (3.21 ± 0.05) × 1011 particles/mL. Thirty-two ejaculates from four Kundhi buffalo bulls were pooled and extended with a Tris extender supplemented with 0, 25, 50, 100, or 200 μg/mL sEV-enriched preparation before cryopreservation. Post-thaw sperm quality, early apoptosis, DNA fragmentation, lipid peroxidation, antioxidant enzymes, and relative mRNA abundance of HSP70 and PRM1 were assessed. All evaluated post-thaw variables differed (P < 0.05) after supplementation, whereas 50 μg/mL revealed the strongest response. The EV-50 group showed higher total motility, progressive motility, viability, and HOST-positive spermatozoa, however reduced early apoptotic sperm, DNA fragmentation, and MDA concentration than the control group. EV-50 also enhanced SOD, catalase, total glutathione, HSP70 and PRM1 expression (1.91 ± 0.07-fold and 1.69 ± 0.05-fold, respectively). In fertility validation, pregnancy rate increased from 41.7% in the control group to 56.7% in the EV-50-treated semen group, with higher odds of pregnancy (OR = 1.83; P = 0.028). In conclusion, supplementation with 50 μg/mL of the sEV-enriched preparation improved post-thaw sperm quality, redox homeostasis, DNA integrity, HSP70 and PRM1 transcript abundance, and field fertility, supporting its potential as a cryopreservation supplement for enhancing the reproductive performance of Kundhi buffalo semen.