Literature DB >> 9363718

Greater numbers of human spermatozoa associate with endosalpingeal cells derived from the isthmus compared with those from the ampulla.

H S Baillie1, A A Pacey, M A Warren, I W Scudamore, C L Barratt.   

Abstract

A simple co-culture bioassay system was used to investigate whether or not the anatomical origin affected the ability of epithelial cells from the human uterine (Fallopian) tube to 'bind' spermatozoa. This study was also used to identify some of the factors which may be involved in the regulation of sperm-epithelial interactions in vitro by comparing different tissue culture models and assessing the effect of oestradiol concentration. Epithelial explants harvested from different regions of human uterine tubes were co-incubated with a known concentration of motile donor spermatozoa. All results were adjusted to reflect a standard sperm concentration of 5 x 10(6)/ml. More spermatozoa associated per field of isthmic compared to ampullary epithelium [isthmus 9.5 +/- 0.9, ampulla 7.1 +/- 0.7 (mean +/- SEM); n = 36, P < 0.05, ANOVA] and cells from post-menopausal patients had an apparently reduced ability to bind spermatozoa [isthmus 5.5 +/- 2.0, ampulla 4.3 +/- 1.4 (mean +/- SEM); n = 4]. Neither menstrual cycle stage nor addition of mid-cycle concentrations of 17beta-oestradiol (750 pmol/l) affected the number of spermatozoa which bound to epithelium from either tubal region. In addition, the number of spermatozoa which bound per field of polarized explants was greater (P < 0.05) than that bound to dissociated primary and passaged epithelial cell monolayers. This report is the first to provide evidence suggestive of a role for sperm-epithelial binding in the formation of an isthmic sperm reservoir in the human uterine tube. Results also indicate that oestrogen is not involved in the regulation of these interactions, and that cell polarity is an important factor for such associations in vitro.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9363718     DOI: 10.1093/humrep/12.9.1985

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  7 in total

Review 1.  Roles of the oviduct in mammalian fertilization.

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

2.  Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation.

Authors:  Tadasuke Oh-Oka; Dinesh Kumar Saxena; Ichiro Tanii; Kazuya Yoshinaga; Kiyotaka Toshimori
Journal:  Reprod Med Biol       Date:  2003-04-30

Review 3.  Sperm preparation: state-of-the-art--physiological aspects and application of advanced sperm preparation methods.

Authors:  Ralf Henkel
Journal:  Asian J Androl       Date:  2011-12-05       Impact factor: 3.285

Review 4.  Simulating nature in sperm selection for assisted reproduction.

Authors:  Erica T Y Leung; Cheuk-Lun Lee; Xinyi Tian; Kevin K W Lam; Raymond H W Li; Ernest H Y Ng; William S B Yeung; Philip C N Chiu
Journal:  Nat Rev Urol       Date:  2021-11-05       Impact factor: 14.432

5.  Prenatal Bisphenol A Exposure Alters Epithelial Cell Composition in the Rhesus Macaque Fetal Oviduct.

Authors:  Pei-Hsuan Hung; Laura S Van Winkle; Carmen J Williams; Patricia A Hunt; Catherine A VandeVoort
Journal:  Toxicol Sci       Date:  2019-02-01       Impact factor: 4.849

6.  Partial Sperm beta1 Integrin Subunit Deletion Proves its Involvement in Mouse Gamete Adhesion/Fusion.

Authors:  Virginie Barraud-Lange; Côme Ialy-Radio; Céline Chalas; Isabelle Holtzmann; Jean-Philippe Wolf; Sandrine Barbaux; Ahmed Ziyyat
Journal:  Int J Mol Sci       Date:  2020-11-11       Impact factor: 5.923

Review 7.  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

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.