Effect of estrogens on boar sperm capacitation in vitro

. 2010 Jul 13 ; 8 () : 87. [epub] 20100713

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid20626847

BACKGROUND: Mammalian sperm must undergo a series of controlled molecular processes in the female reproductive tract called capacitation before they are capable of penetrating and fertilizing the egg. Capacitation, as a complex biological process, is influenced by many molecular factors, among which steroidal hormone estrogens play their role. Estrogens, present in a high concentration in the female reproductive tract are generally considered as primarily female hormones. However, there is increasing evidence of their important impact on male reproductive parameters. The purpose of this study is to investigate the effect of three natural estrogens such as estrone (E1), 17beta-estradiol (E2) and estriol (E3) as well as the synthetical one, 17 alpha-ethynylestradiol (EE2) on boar sperm capacitation in vitro. METHODS: Boar sperm were capacitated in vitro in presence of estrogens. Capacitation progress in control and experimental samples was analyzed by flow cytometry with the anti-acrosin monoclonal antibody (ACR.2) at selected times of incubation. Sperm samples were analyzed at 120 min of capacitation by CTC (chlortetracycline) assay, immunocytochemistry and flow cytometry with anti-acrosin ACR.2 antibody. Furthermore, sperm samples and capacitating media were analyzed by immunocytochemistry, ELISA with the ACR.2 antibody, and the acrosin activity assay after induced acrosomal reaction (AR). RESULTS: Estrogens stimulate sperm capacitation of boar sperm collected from different individuals. The stimulatory effect depends on capacitation time and is highly influenced by differences in the response to estrogens such as E2 by individual animals. Individual estrogens have relatively same effect on capacitation progress. In the boar samples with high estrogen responsiveness, estrogens stimulate the capacitation progress in a concentration-dependent manner. Furthermore, estrogens significantly increase the number of acrosome-reacted sperm after zona pellucida- induced acrosomal reaction. CONCLUSIONS: We demonstrate here the stimulatory effect of four different estrogens on boar sperm capacitation in vitro. According to our results, there is significant difference in the response to tested estrogens at different capacitation time and among individual animals. In animals with a high response to estrogens, there is a concentration-dependent stimulation of capacitation and individual estrogens have relatively the same effect. Effects of individual estrogens, differences in the response to them by individual animals, their time and concentration-dependent outcomes further contribute to our knowledge about steroidal action in sperm.

Zobrazit více v PubMed

Austin CR. Observation on penetration of sperm into the mammalian egg. Aust J Sci Res. 1951;4:581–596. PubMed

Austin CR. Capacitation of spermatozoa. Int J Fertil. 1967;12:25–31. PubMed

Chang MC. Ferilizing capacity of spermatozoa deposited into the Fallopian tubes. Nature. 1951;168:997–998. doi: 10.1038/168697b0. PubMed DOI

Hunter RH, Hall JP. Capacitation of boar spermatozoa: synergism between uterine and tubal environments. J Exp Zool. 1974;188(2):203–213. doi: 10.1002/jez.1401880208. PubMed DOI

Brown SM, Hamner CE. Capacitation of sperm in the female reproductive tract of the rabbit during estrus and pseudopregnancy. Fertil Steril. 1971;22(2):92–97. PubMed

Yanagimachi R. In vitro capacitation of hamster spermatozoa by follicular fluid. J Reprod Fertil. 1969;18(2):275–286. doi: 10.1530/jrf.0.0180275. PubMed DOI

Niwa K, Imai H, Kim CI, Iritani A. Fertilization in vitro of hamster and mouse eggs in a chemically defined medium. J Reprod Fertil. 1980;58(1):109–114. doi: 10.1530/jrf.0.0580109. PubMed DOI

Eddy EM, Washburn TF, Bunch DO, Goulding EH, Gladen BC, Lubahn DB, Korach KS. Targeted disruption of the estrogen receptor gene in male mice causes alteration of spermatogenesis and infertility. Endocrinology. 1996;137(11):4796–4805. doi: 10.1210/en.137.11.4796. PubMed DOI

Acconcia F, Kumar R. Signaling regulation of genomic and nongenomic functions of estrogen receptors. Cancer Lett. 2006;8; 238(1):1–14. doi: 10.1016/j.canlet.2005.06.018. PubMed DOI

Aquila S, Sisci D, Gentile M, Middea E, Catalano S, Carpino A, Rago V, Andò S. Estrogen receptor (ER) alpha and ER beta are both expressed in human ejaculated spermatozoa: evidence of their direct interaction with phosphatidylinositol-3-OH kinase/Akt pathway. J Clin Endocrinol Metab. 2004;89(3):1443–1451. doi: 10.1210/jc.2003-031681. PubMed DOI

Naz RK, Sellamuthu R. Receptors in spermatozoa: are they real? J Androl. 2006;27(5):627–636. doi: 10.2164/jandrol.106.000620. PubMed DOI

Rago V, Aquila S, Panza R, Carpino A. Cytochrome P450arom, androgen and estrogen receptors in pig sperm. Reprod Biol Endocrinol. 2007;5:23. doi: 10.1186/1477-7827-5-23. PubMed DOI PMC

Luconi M, Francavilla F, Porazzi I, Macerola B, Forti G, Baldi E. Human spermatozoa as a model for studying membrane receptors mediating rapid nongenomic effects of progesterone and estrogens. Steroids. 2004;69(8-9):553–559. doi: 10.1016/j.steroids.2004.05.013. PubMed DOI

Gwatkin RB, Williams DT. Inhibition of Sperm Capacitation in vitro by Contraceptive Steroids. Nature. 1970;227(5254):182–183. doi: 10.1038/227182a0. PubMed DOI

Briggs MH. Steroid hormones and the fertilizing capacity of spermatozoa. Steroids. 1973;22(4):547–553. doi: 10.1016/0039-128X(73)90010-X. PubMed DOI

Bathla H, Guraya SS, Sangha GK. Role of estradiol in the capacitation and acrosome reaction of hamster epididymal spermatozoa in the isolated uterus of mice incubated in vitro. Indian J Physiol Pharmacol. 1999;43(2):211–217. PubMed

Hamner CE, Wilson LA Jr. Inhibition of capacitation in the rabbit. Fertil Steril. 1972;23(3):196–200. PubMed

Adeoya-Osiguwa SA, Markoulaki S, Pocock V, Milligan SR, Fraser LR. 17beta-Estradiol and environmental estrogens significantly affect mammalian sperm function. Hum Reprod. 2003;18(1):100–107. doi: 10.1093/humrep/deg037. PubMed DOI

Francavilla F, Romano R, Pandolfi C, Macerola B, Santucci R, Necozione S, Francavilla S. Evaluation of the effect of 17alphaOH-progesterone and 17beta-oestradiol on human sperm ability to fuse with oocytes: comparison and possible interference with the effect of progesterone. Int J Androl. 2003;26(6):342–347. doi: 10.1111/j.1365-2605.2003.00435.x. PubMed DOI

Wang WH, Abeydeera LR, Fraser LR, Niwa K. Functional analysis using chlortetracycline fluorescence and in vitro fertilization of frozen-thawed ejaculated boar spermatozoa incubated in a protein-free chemically defined medium. J Reprod Fertil. 1995;104(2):305–313. doi: 10.1530/jrf.0.1040305. PubMed DOI

Fraser LR, Abeydeera LR, Niwa K. Ca(2+)-regulating mechanisms that modulate bull sperm capacitation and acrosomal exocytosis as determined by chlortetracycline analysis. Mol Reprod Dev. 1995;40(2):233–241. doi: 10.1002/mrd.1080400213. PubMed DOI

Peknicová J, Moos J. Monoclonal antibodies against boar acrosomal antigens labelling undamaged acrosomes of spermatozoa in immunofluorescence test. Andrologia. 1990;22(5):427–435. PubMed

Peknicova J, Moos J, Mollova M, Srsen V, Capkova J. Changes in immunochemical localisation of acrosomal and sperm proteins in boar spermatozoa during capacitation and induced acrosome reaction. Anim Repr Sci. 1994;35:255–271. doi: 10.1016/0378-4320(94)90041-8. DOI

De Jonge C. Biological basis for human capacitation. Hum Reprod Update. 2005;11(3):205–214. doi: 10.1093/humupd/dmi010. PubMed DOI

Baldi E, Luconi M, Muratori M, Marchiani S, Tamburrino L, Forti G. Nongenomic activation of spermatozoa by steroid hormones: facts and fictions. Mol Cell Endocrinol. 2009;308(1-2):39–46. doi: 10.1016/j.mce.2009.02.006. PubMed DOI

Nawata H, Chong MT, Bronzert D, Lippman ME. Estradiol-independent growth of a subline of MCF-7 human breast cancer cells in culture. J Biol Chem. 1981;256(13):6895–902. PubMed

Blair RM, Fang H, Branham WS, Hass BS, Dial SL, Moland CL, Tong W, Shi L, Perkins R, Sheehan DM. The estrogen receptor relative binding affinities of 188 natural and xenochemicals: structural diversity of ligands. Toxicol Sci. 2000. pp. 138–153. PubMed DOI

Nishimura I, Ui-Tei K, Saigo K, Ishii H, Sakuma Y, Kato M. 17-Estradiol at Physiological Concentrations Augments Ca2+-Activated K+ Currents via Estrogen Receptor in the gonadotropin-Releasing Hormone Neuronal Cell Line GT1-7. Endocrinology. 2008;149(2):774–782. doi: 10.1210/en.2007-0759. PubMed DOI

Tarlatzis BC, Pazaitou K, Bili H, Bontis J, Papadimas J, Lagos S, Spanos E, Mantalenakis S. Growth hormone, oestradiol, progesterone and testosterone concentrations in follicular fluid after ovarian stimulation with various regimes for assisted reproduction. Hum Reprod. 1993;8(10):1612–1616. PubMed

Ouellette Y, Price CA, Carrière PD. Follicular fluid concentration of transforming growth factor-beta1 is negatively correlated with estradiol and follicle size at the early stage of development of the first-wave cohort of bovine ovarian follicles. Domest Anim Endocrinol. 2005;29(4):623–633. doi: 10.1016/j.domaniend.2005.04.008. PubMed DOI

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

17α-Ethynylestradiol alters testicular epigenetic profiles and histone-to-protamine exchange in mice

. 2024 Nov 04 ; 22 (1) : 135. [epub] 20241104

Missing Information from the Estrogen Receptor Puzzle: Where Are They Localized in Bull Reproductive Tissues and Spermatozoa?

. 2020 Jan 10 ; 9 (1) : . [epub] 20200110

Fluorescent analysis of boar sperm capacitation process in vitro

. 2019 Dec 19 ; 17 (1) : 109. [epub] 20191219

Compartmentalization of the proteasome-interacting proteins during sperm capacitation

. 2019 Aug 29 ; 9 (1) : 12583. [epub] 20190829

New Insight into Sperm Capacitation: A Novel Mechanism of 17β-Estradiol Signalling

. 2018 Dec 12 ; 19 (12) : . [epub] 20181212

Of Oestrogens and Sperm: A Review of the Roles of Oestrogens and Oestrogen Receptors in Male Reproduction

. 2017 Apr 25 ; 18 (5) : . [epub] 20170425

Evaluation of the expression of sperm proteins in normozoospermic and asthenozoospermic men using monoclonal antibodies

. 2016 Jan-Feb ; 18 (1) : 108-13.

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...