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Biology of reproduction2018; 99(6); 1194-1204; doi: 10.1093/biolre/ioy149

Source and localization of ovulation-inducing factor/nerve growth factor in male reproductive tissues among mammalian species.

Abstract: The objectives of the study were to compare the presence and localization of ovulation-inducing factor (OIF)/nerve growth factor (NGF) in male reproductive organs and determine the abundance in ejaculates of species representative of both spontaneous and induced ovulators. We hypothesized that the protein is a widely conserved component of semen among mammals, but is most abundant in camelids. Immunohistochemical analysis was performed on tissues from the male reproductive system of llamas, rats, cattle, bison, elk, and white-tailed deer (n = 2 males/species), and the abundance of OIF/NGF in the seminal plasma of camelids (llamas and alpacas), cattle, horses, and pigs (n = 69, 53, 24, and 16 ejaculates, respectively) were quantified by radioimmunoassay. Based on immunoreactivity in both the glandular epithelium and glandular lumen, the prostate gland was the main source of seminal OIF/NGF in llamas, the vesicular gland and ampullae in bovids (cattle and bison), and the ampullae and prostate in cervids (elk and white-tailed deer). Camelid and bovine seminal plasma induced dendritic growth in the PC12 differentiation bioassay, but no effect was observed with equine or porcine seminal plasma. The concentration of OIF/NGF was 10 times higher in camelid than bovine seminal plasma (1.2 ± 0.21 vs. 0.10 ± 0.03; P < 0.05); OIF/NGF was not detected in equine or porcine ejaculates by radioimmunoassay. Based on tissue localization, abundance, and bioactivity, we conclude that OIF/NGF is a common protein within the male accessory glands among species, and its abundance in camelids, bovids, and cervids suggests an important role in the mechanisms of ovulation in both induced and spontaneous ovulators.
Publication Date: 2018-07-10 PubMed ID: 29982342DOI: 10.1093/biolre/ioy149Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article is aimed at comparing the presence and localization of the ovulation-inducing factor (OIF)/nerve growth factor (NGF) in the male reproductive organs among different species. The results indicated that this protein is common among mammals, but it is most abundant in camelids.

Research Overview

  • The study compared the presence and localization of ovulation-inducing factor (OIF) or nerve growth factor (NGF) in the male reproductive organs across different species.
  • The research included species that exhibit both spontaneous and induced ovulation, to ascertain the role of OIF/NGF in the ovulation process.
  • The species involved were llamas, rats, cattle, bison, elk, white-tailed deer, alpacas, horses, and pigs.

Methodology

  • Immunohistochemical analysis was used on tissue from the male reproductive system of two male individuals of each species.
  • The abundance of OIF/NGF in the seminal plasma of camelids (llamas and alpacas), cattle, horses, and pigs was quantified using a radioimmunoassay method.

Findings

  • The study found that the prostate gland was the main producer of seminal OIF/NGF in llamas, the vesicular gland and ampullae in bovids (cattle and bison), and the ampullae and prostate in cervids (elk and white-tailed deer).
  • The seminal plasma of camelids and bovine induced dendritic growth in a PC12 differentiation bioassay, which evaluates the potential of these compounds to stimulate cell differentiation.
  • However, equine and porcine seminal plasma did not demonstrate any effect on this bioassay.
  • The concentration of OIF/NGF in camelid seminal plasma was ten times higher than in bovine seminal plasma.
  • OIF/NGF was not detected in equine or porcine ejaculates in the radioimmunoassay trials.

Conclusion

  • The study concluded that OIF/NGF is a commonly found protein within the male accessory glands across different species.
  • Its notable abundance in camelids, bovids, and cervids indicates its role in the mechanisms of ovulation, irrespective of whether the ovulation is spontaneous or induced.

Cite This Article

APA
Bogle OA, Carrasco RA, Ratto MH, Singh J, Adams GP. (2018). Source and localization of ovulation-inducing factor/nerve growth factor in male reproductive tissues among mammalian species. Biol Reprod, 99(6), 1194-1204. https://doi.org/10.1093/biolre/ioy149

Publication

ISSN: 1529-7268
NlmUniqueID: 0207224
Country: United States
Language: English
Volume: 99
Issue: 6
Pages: 1194-1204

Researcher Affiliations

Bogle, Orleigh A
  • Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Carrasco, Rodrigo A
  • Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Ratto, Marcelo H
  • Department of Animal Science, Universidad Austral de Chile, Valdivia, Chile.
Singh, Jaswant
  • Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Adams, Gregg P
  • Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

MeSH Terms

  • Animals
  • Antibodies
  • Genitalia, Male / metabolism
  • Male
  • Mammals / physiology
  • Nerve Growth Factor / metabolism
  • Semen / chemistry
  • Semen / metabolism
  • Species Specificity

Citations

This article has been cited 6 times.
  1. Paiva L, Silva M, Carrasco R, Ratto V, Goicochea J, Ratto M. Seminal plasma nerve growth factor signaling on the reproductive physiology of female llamas.. Anim Reprod 2022;19(4):e20220116.
    doi: 10.1590/1984-3143-AR2022-0116pubmed: 36819481google scholar: lookup
  2. Rimayanti R, Azizah N, Srianto P, Madyawati SP, Sardjito T, Mustofa I. Serum Nerve Growth Factor Levels as a Predictor of Bull Candidate Semen Quality of Madura Cattle.. Vet Med Int 2022;2022:7128384.
    doi: 10.1155/2022/7128384pubmed: 35449725google scholar: lookup
  3. Maranesi M, Boiti C, Zerani M. Nerve Growth Factor (NGF) and Animal Reproduction.. Adv Exp Med Biol 2021;1331:277-287.
    doi: 10.1007/978-3-030-74046-7_19pubmed: 34453306google scholar: lookup
  4. Lough-Stevens M, Ghione CR, Urness M, Hobbs A, Sweeney CM, Dean MD. Male-derived copulatory plugs enhance implantation success in female Mus musculus.. Biol Reprod 2021 Mar 11;104(3):684-694.
    doi: 10.1093/biolre/ioaa228pubmed: 33355341google scholar: lookup
  5. Valderrama X, Ulloa-Leal C, Silva ME, Goicochea J, Apichela S, Argañaraz M, Sari L, Paiva L, Ratto VF, Ratto MH. β-NGF Stimulates Steroidogenic Enzyme and VEGFA Gene Expression, and Progesterone Secretion via ERK 1/2 Pathway in Primary Culture of Llama Granulosa Cells.. Front Vet Sci 2020;7:586265.
    doi: 10.3389/fvets.2020.586265pubmed: 33195615google scholar: lookup
  6. Maranesi M, Palermo FA, Bufalari A, Mercati F, Paoloni D, Cocci P, Moretti G, Crotti S, Zerani M, Dall'Aglio C. Seasonal Expression of NGF and Its Cognate Receptors in the Ovaries of Grey Squirrels (Sciurus carolinensis).. Animals (Basel) 2020 Sep 2;10(9).
    doi: 10.3390/ani10091558pubmed: 32887345google scholar: lookup