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General and comparative endocrinology2014; 200; 35-43; doi: 10.1016/j.ygcen.2014.02.016

Stallion spermatozoa: putative target of estrogens; presence of the estrogen receptors ESR1, ESR2 and identification of the estrogen-membrane receptor GPER.

Abstract: Among mammals, the stallion produces the largest amount of testicular estrogens. These steroid hormones are produced mainly by Leydig and Sertoli cells in the testis and also in the epididymis. Their role in horse testicular physiology and their ability to act on spermatozoa are still unknown. In order to determine if spermatozoa are targets for estrogens, the presence of estrogen receptors in mature ejaculated spermatozoa has been investigated. The presence of a single isoform of ESR1 (66kDa) and ESR2 (61kDa) was found by Western-blot analysis in samples from seven stallions. Confocal analysis mainly showed a flagellar localization for both receptors. Immuno-TEM experiments revealed that they are mostly located near the membranes, which are classically associated with rapid, non-genomic, effects. Moreover, we evidenced the expression of the seven transmembrane estradiol binding receptor GPER in colt testis. The protein was also localized at the connecting piece in mature spermatozoa. In conclusion, our results suggest that horse spermatozoa are a target for estrogens, which could act on several receptors either during the epididymal transit and/or in the female genital tract.
Publication Date: 2014-03-04 PubMed ID: 24607572DOI: 10.1016/j.ygcen.2014.02.016Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the presence of estrogen receptors in horse spermatozoa and suggests that these can be targets for estrogens, which could potentially influence the sperm during its journey through the epididymis or within the female genital tract.

Understanding Horse Testicular Physiology

  • The study hinges on understanding how the body of a stallion, a male horse, produces and uses estrogens, a type of steroid hormone. Among mammals, stallions produce the largest amount of these hormones. They’re created mainly in Leydig and Sertoli cells located in the testis and in the epididymis, a tube where sperm cells are stored and mature.
  • Until now, the role of estrogens in horse testicular physiology has been unclear, as is their potential capacity to act on spermatozoa. The researchers set out to find out if the sperm cells are targets for estrogens by investigating the presence of estrogen receptors on mature, ejaculated spermatozoa.

Presence of Estrogen Receptors

  • The researchers found the existence of a single isoform of two estrogen receptors, ESR1 (66kDa) and ESR2 (61kDa), by applying a technique known as Western-blot analysis on samples gathered from seven stallions.
  • Using a different technique called confocal analysis, they discovered that these receptors are primarily located in the flagellar region of the sperm cells, which is the part that enables the movement of the cell.
  • Immuno-TEM experiments, another kind of analysis, further revealed that the receptors were found mostly near the membranes, locations typically associated with rapid, non-genomic effects.

Discovery of GPER in Colt Testis

  • Besides discovering ESR1 and ESR2, the researchers also found the expression of the seven transmembrane estradiol binding receptor GPER in the testis of a young horse, or colt.
  • Like the other receptors, this protein too was localized at the connecting piece in mature spermatozoa.

Conclusion

  • The findings of this research propose that stallion spermatozoa could be a target for estrogens. The observation that the receptors are located at the membrane and connecting piece of the spermatozoa suggests that the estrogens could potentially act on these receptors during the sperm’s transit through the epididymis or within the female reproductive system.

Cite This Article

APA
Arkoun B, Gautier C, Delalande C, Barrier-Battut I, Guénon I, Goux D, Bouraïma-Lelong H. (2014). Stallion spermatozoa: putative target of estrogens; presence of the estrogen receptors ESR1, ESR2 and identification of the estrogen-membrane receptor GPER. Gen Comp Endocrinol, 200, 35-43. https://doi.org/10.1016/j.ygcen.2014.02.016

Publication

ISSN: 1095-6840
NlmUniqueID: 0370735
Country: United States
Language: English
Volume: 200
Pages: 35-43
PII: S0016-6480(14)00059-8

Researcher Affiliations

Arkoun, Brahim
  • Normandie Univ, F-14032 Caen, France; UNICAEN, EA2608, OeReCa, F-14032 Caen, France; USC-INRA 2006, F-14032 Caen, France.
Gautier, Camille
  • Normandie Univ, F-14032 Caen, France; UNICAEN, EA2608, OeReCa, F-14032 Caen, France; USC-INRA 2006, F-14032 Caen, France.
Delalande, Christelle
  • Normandie Univ, F-14032 Caen, France; UNICAEN, EA2608, OeReCa, F-14032 Caen, France; USC-INRA 2006, F-14032 Caen, France.
Barrier-Battut, Isabelle
  • Jumenterie du Pin, Institut Français du Cheval et de l'Equitation, 61310 Exmes, France.
Guénon, Isabelle
  • Normandie Univ, F-14032 Caen, France; UNICAEN, EA2608, OeReCa, F-14032 Caen, France; USC-INRA 2006, F-14032 Caen, France.
Goux, Didier
  • Normandie Univ, F-14032 Caen, France; UNICAEN, CMABIO, F-14032 Caen, France.
Bouraïma-Lelong, Hélène
  • Normandie Univ, F-14032 Caen, France; UNICAEN, EA2608, OeReCa, F-14032 Caen, France; USC-INRA 2006, F-14032 Caen, France. Electronic address: helene.bouraima@unicaen.fr.

MeSH Terms

  • Animals
  • Blotting, Western
  • Cell Membrane / metabolism
  • Ejaculation
  • Estrogens / metabolism
  • Female
  • Flow Cytometry
  • Gene Expression Regulation
  • Horses / metabolism
  • Immunohistochemistry
  • Male
  • Protein Transport
  • Receptors, Estrogen / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Spermatozoa / cytology
  • Spermatozoa / metabolism
  • Spermatozoa / ultrastructure
  • Subcellular Fractions / metabolism

Citations

This article has been cited 8 times.
  1. Chimento A, De Luca A, Nocito MC, Avena P, La Padula D, Zavaglia L, Pezzi V. Role of GPER-Mediated Signaling in Testicular Functions and Tumorigenesis.. Cells 2020 Sep 17;9(9).
    doi: 10.3390/cells9092115pubmed: 32957524google scholar: lookup
  2. Zhang D, Wang Y, Lin H, Sun Y, Wang M, Jia Y, Yu X, Jiang H, Xu W, Sun JP, Xu Z. Function and therapeutic potential of G protein-coupled receptors in epididymis.. Br J Pharmacol 2020 Dec;177(24):5489-5508.
    doi: 10.1111/bph.15252pubmed: 32901914google scholar: lookup
  3. Tang D, Bao J, Bai G, Hao M, Jin R, Liu F. The AGT Haplotype of the ESR2 Gene Containing the Polymorphisms rs2077647A, rs4986938G, and rs1256049T Increases the Susceptibility of Unexplained Recurrent Spontaneous Abortion in Women in the Chinese Hui Population.. Med Sci Monit 2020 May 2;26:e921102.
    doi: 10.12659/MSM.921102pubmed: 32359133google scholar: lookup
  4. Antalikova J, Secova P, Horovska L, Krejcirova R, Simonik O, Jankovicova J, Bartokova M, Tumova L, Manaskova-Postlerova P. Missing Information from the Estrogen Receptor Puzzle: Where Are They Localized in Bull Reproductive Tissues and Spermatozoa?. Cells 2020 Jan 10;9(1).
    doi: 10.3390/cells9010183pubmed: 31936899google scholar: lookup
  5. Skibinska I, Andrusiewicz M, Soin M, Jendraszak M, Urbaniak P, Jedrzejczak P, Kotwicka M. Increased expression of PELP1 in human sperm is correlated with decreased semen quality.. Asian J Androl 2018 Sep-Oct;20(5):425-431.
    doi: 10.4103/aja.aja_11_18pubmed: 29676290google scholar: lookup
  6. Cooke PS, Nanjappa MK, Ko C, Prins GS, Hess RA. Estrogens in Male Physiology.. Physiol Rev 2017 Jul 1;97(3):995-1043.
    doi: 10.1152/physrev.00018.2016pubmed: 28539434google scholar: lookup
  7. Hess RA. Small tubules, surprising discoveries: from efferent ductules in the turkey to the discovery that estrogen receptor alpha is essential for fertility in the male.. Anim Reprod 2015 Jan-Mar;12(1):7-23.
    pubmed: 28191043
  8. Kotwicka M, Skibinska I, Jendraszak M, Jedrzejczak P. 17β-estradiol modifies human spermatozoa mitochondrial function in vitro.. Reprod Biol Endocrinol 2016 Aug 26;14(1):50.
    doi: 10.1186/s12958-016-0186-5pubmed: 27565707google scholar: lookup