Ouabain-induced activation of phospholipase C zeta and its contributions to bovine sperm capacitation

Author(s):  
Veena Unnikrishnan ◽  
John P Kastelic ◽  
Jacob C Thundathil
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Rasoul Kowsar ◽  
Shahrzad Ronasi ◽  
Nima Sadeghi ◽  
Khaled Sadeghi ◽  
Akio Miyamoto

AbstractUpon insemination, sperm cells are exposed to components of the female reproductive tract (FRT) fluids, such as urea and epidermal growth factor (EGF). It has been shown that both urea and EGF use EGF receptor signaling and produce reactive oxygen species (ROS) that are required at certain levels for sperm capacitation and acrosome reaction. We therefore hypothesized that during bovine sperm capacitation, a high level of urea and EGF could interfere with sperm function through overproduction of ROS. High-level urea (40 mg/dl urea is equal to 18.8 mg/dl of blood urea nitrogen) significantly increased ROS production and TUNEL-positive sperm (sperm DNA fragmentation, sDF) percentage, but decreased HOS test score, progressive motility, acrosome reaction and capacitation. The EGF reversed the negative effects of urea on all sperm parameters, with the exception of ROS production and DNA fragmentation, which were higher in urea-EGF-incubated sperm than in control-sperm. The developmental competence of oocytes inseminated with urea-EGF-incubated sperm was significantly reduced compared to the control. A close association of ROS production or sDF with 0-pronuclear and sperm non-capacitation rates was found in the network analysis. In conclusion, EGF enhanced urea-reduced sperm motility; however, it failed to reduce urea-increased sperm ROS or sDF levels and to enhance subsequent oocyte competence. The data suggests that any study to improve sperm quality should be followed by a follow-up assessment of the fertilization outcome.


2008 ◽  
Vol 78 (Suppl_1) ◽  
pp. 187-187
Author(s):  
Nir Etkovitz ◽  
Tali Rotman ◽  
Sara Rubinstein ◽  
Haim Breitbart

Zygote ◽  
2020 ◽  
Vol 28 (6) ◽  
pp. 489-494
Author(s):  
Paula Rodríguez-Villamil ◽  
Daiane Mentz ◽  
Felipe Ledur Ongaratto ◽  
Luis Henrique Aguiar ◽  
Jose Luiz Rodrigues ◽  
...  

SummaryThe present study evaluated the effect of binder of sperm protein 1 (BSP1) and/or heparin on in vitro bovine capacitation and fertilization rates using epididymal and ejaculated bovine sperm. Frozen–thawed sperm were selected and used in the following treatments. Control group: Fert-TALP medium without heparin; heparin (HEP) group: Fert-TALP with heparin (10 UI/ml); BSP1 group: Fert-TALP medium with BSP1 (10 µg/ml for ejaculated sperm; 40 µg/ml for epididymal sperm); HEP + BSP1 group: Fert-TALP medium with heparin (5 UI/ml) and BSP1 (5 µg/ml for ejaculated sperm; 20 µg/ml for epididymal sperm) and determined in vitro capacitation rates in different interval times (0, 15, 30 and 60 min) using the chlortetracycline fluorescence (CTC) method. Also, we evaluated the development rates of oocytes fertilized with ejaculated or epididymal sperm into the same treatments. Capacitation was greater and faster when ejaculated sperm were treated for 60 min with heparin compared with other treatments. However, developmental rates were similar in all treatments. For epididymal sperm, the treatments with BSP1 presented higher capacitation and fertilization rates compared with heparin (P < 0.05). The effects of heparin + BSP1 on capacitation and developmental rates did not cause any increase in capacitation or blastocyst rates compared with other groups for ejaculated or epididymal sperm. In conclusion, this study confirmed that either BSP1 and heparin can be used as capacitator agents for bovine ejaculated sperm during IVF. However, BSP1 seems to be more efficient compared with heparin for epididymal sperm. Furthermore, BSP1 and heparin have no synergic effects on sperm capacitation.


2017 ◽  
Vol 29 (1) ◽  
pp. 193
Author(s):  
M. M. Elsokary ◽  
D. J. Miller

After mating, sperm move from the site of semen deposition towards the oviduct, where sperm are stored before fertilization. Much of the literature indicates that oviduct glycans bind sperm to retain them in the oviduct reservoir. We have discovered that a specific oviduct glycan on the epithelium (sulfated Lewis A trisaccharide; suLeA) binds bovine sperm and maintains sperm viability. But the way in which sperm are released from oviduct epithelial glycans to fertilize oocytes is enigmatic. In this study, we tested the hypothesis that oocytes signal the release of sperm from an oviduct glycan (suLeA) on a bead and that the released sperm could fertilize the oocytes. Sepharose beads with avidin on their surface were used to immobilize biotinylated suLeA. After coupling, the beads were washed. Frozen bovine semen was thawed, and sperm were washed and allowed to bind to suLeA-coated beads for 1 h in capacitating medium at 39°C. Mature bovine oocytes were then prewashed with the same medium (without heparin) and added to droplets with sperm bound to beads and incubated for 18 h at 5% CO2 at 38.5°C. Bound sperm (mean = 4 per bead) were enumerated before and after oocyte addition. A control using dead (fixed) oocytes was also used. Three independent replicates were tested using 125 oocytes for each treatment. Data were analysed by ANOVA. The addition of live oocytes released 68.1% of the sperm bound to beads, whereas only 18.8% of sperm were released by addition of dead oocytes (control; P < 0.05). If heparin for sperm capacitation (3.125 g mL−1 final concentration) was added concurrently with the addition of live oocytes to sperm bound to beads, the majority of bound sperm were released (87.7%), whereas dead oocytes (control) released fewer sperm (67.3% sperm, P < 0.05). Thus, both heparin and oocytes released sperm from beads independently but, together, they released the greatest number of sperm. Altogether, our results indicate that, in addition to heparin, mature oocytes induce sperm release from immobilized oviduct glycans for fertilization. This is the first demonstration that oocytes can signal sperm release from oviduct glycans in any mammal.


2019 ◽  
Vol 54 (12) ◽  
pp. 1612-1620 ◽  
Author(s):  
Valter Luiz Maciel ◽  
Maria Clara Caldas‐Bussiere ◽  
Diego Fernando Dubeibe Marín ◽  
Carla Sobrinho Paes de Carvalho ◽  
Celia Raquel Quirino ◽  
...  

Andrologia ◽  
2002 ◽  
Vol 34 (2) ◽  
pp. 91-97 ◽  
Author(s):  
C. M. O'Flaherty ◽  
N. B. Beorlegui ◽  
M. T. Beconi

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