Literature DB >> 11868811

Binding regulation of porcine spermatozoa to oviductal vesicles in vitro.

Mariève Bureau1, Janice L Bailey, Marc-André Sirard.   

Abstract

In vivo, en route to the site of fertilization, mammalian spermatozoa bind to oviduct epithelial cells (OECs). This binding may favor sperm survival and capacitation, but little is known about the regulation of detachment of sperm from the oviduct in vivo. Therefore, we studied sperm-oviduct interaction in vitro using vesicles formed from OECs in primary culture. Porcine oviducts were collected from gilts at the slaughterhouse. OECs were obtained by compressing the oviduct and culturing them in TCM-199 medium with 10% fetal calf serum for 48 hours. For the first experiment, to test the hypothesis that progesterone (P4) and estradiol (E2) affect sperm-OEC binding, OECs were pretreated for 48 hours with 100 ng/mL of P4 or E2. In the second experiment, porcine follicular fluid (pFF, 5%), caffeine (1 microM), calcium ionophore A23187 (1 microM), and DMSO (0.01%) were added to the incubation medium to provide insights on the mechanisms of sperm release from the oviduct. For both experiments, 50 x 10(6) sperm were coincubated with 50 microL of OEC vesicles in 1 mL of incubation medium for up to 24 hours at 37 degrees C and 5% CO2. After an initial 30 minutes of coincubation, the vesicles settled and a sample of the supernatant was removed to evaluate sperm release and acrosomal status; subsequent samples were removed after 2, 4, and 24 hours of coincubation. To evaluate the effect of the different treatments on sperm integrity, the acrosome status of the spermatozoa was determined using fluoresceinlabeled Pisum sativum agglutinin staining. Experiment 1 showed that P4 pretreatment of OECs interferes with sperm binding compared with pretreatment with E2 or controls (P < .05). In experiment 2, coincubation in the presence of A23187 increased sperm detachment compared with pretreatment with DMSO, pFF, caffeine, or controls (P < .05). For each experiment, the treatments did not affect the percentage of acrosome-reacted sperm compared with controls (P < .05).

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Year:  2002        PMID: 11868811

Source DB:  PubMed          Journal:  J Androl        ISSN: 0196-3635


  6 in total

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Authors:  P Coy; F A García-Vázquez; P E Visconti; M Avilés
Journal:  Reproduction       Date:  2012-10-01       Impact factor: 3.906

2.  Progesterone induces porcine sperm release from oviduct glycans in a proteasome-dependent manner.

Authors:  Momal Sharif; Karl Kerns; Peter Sutovsky; Nicolai Bovin; David J Miller
Journal:  Reproduction       Date:  2021-04       Impact factor: 3.906

3.  A transcriptomal analysis of bovine oviductal epithelial cells collected during the follicular phase versus the luteal phase of the estrous cycle.

Authors:  K L Cerny; E Garrett; A J Walton; L H Anderson; P J Bridges
Journal:  Reprod Biol Endocrinol       Date:  2015-08-05       Impact factor: 5.211

4.  Effects of Panax ginseng, zearalenol, and estradiol on sperm function.

Authors:  Sandra L Gray; Brett R Lackey; William R Boone
Journal:  J Ginseng Res       Date:  2015-08-24       Impact factor: 6.060

5.  Release of Porcine Sperm from Oviduct Cells is Stimulated by Progesterone and Requires CatSper.

Authors:  Sergio A Machado; Momal Sharif; Huijing Wang; Nicolai Bovin; David J Miller
Journal:  Sci Rep       Date:  2019-12-20       Impact factor: 4.379

Review 6.  Sperm migration, selection, survival, and fertilizing ability in the mammalian oviduct†.

Authors:  Coline Mahé; Aleksandra Maria Zlotkowska; Karine Reynaud; Guillaume Tsikis; Pascal Mermillod; Xavier Druart; Jennifer Schoen; Marie Saint-Dizier
Journal:  Biol Reprod       Date:  2021-08-03       Impact factor: 4.285

  6 in total

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