Steroidogenic Enzyme and Steroid Receptor Expression in the Equine Accessory Sex Glands

• Published in: Animals (Basel) Vol. 11; no. 8; p. 2322
• Main Authors: Ellerbrock, Robyn E., Podico, Giorgia, Scoggin, Kirsten E., Ball, Barry A., Carossino, Mariano, Canisso, Igor F.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 06-08-2021; MDPI
• Subjects: ampulla; Androgen receptors; Androgens; Animals; Aromatase; Biotechnology; bulbourethral gland; Dehydrogenases; Domestic animals; Enzymes; Estrogen receptors; Estrogens; Fertility; fetus; Fetuses; Gene expression; Glands; Hormones; Horses; Hydroxylase; Hydroxysteroids; Immunohistochemistry; Localization; Monoclonal antibodies; mRNA; Polyclonal antibodies; Polymerase chain reaction; Prostate; Reproductive status; Secretions; Semen; Sex glands; stallion; Steroid hormone receptors; Steroid hormones; Steroidogenesis; Steroids; Testes; vesicular gland; United States > US
• ISSN: 2076-2615; 2076-2615
• DOI: 10.3390/ani11082322

The expression pattern and distribution of sex steroid receptors and steroidogenic enzymes during development of the equine accessory sex glands has not previously been described. We hypothesized that equine steroidogenic enzyme and sex steroid receptor expression is dependent on reproductive status. Accessory sex glands were harvested from mature stallions, pre-pubertal colts, geldings, and fetuses. Expression of mRNA for estrogen receptor 1 (ESR1), estrogen receptor 2 (ESR2), androgen receptor (AR), 3β-Hydroxysteroid dehydrogenase/Δ5-4 isomerase (3βHSD), P450,17α hydroxylase, 17–20 lyase (CYP17), and aromatase (CYP19) were quantified by RT-PCR, and protein localization of AR, ER-α, ER-β, and 3βHSD were investigated by immunohistochemistry. Expression of AR, ESR2, CYP17, or CYP19 in the ampulla was not different across reproductive statuses (p > 0.1), while expression of ESR1 was higher in the ampulla of geldings and fetuses than those of stallions or colts (p < 0.05). AR, ESR1 and ESR2 expression were decreased in stallion vesicular glands compared to the fetus or gelding, while AR, ESR1, and CYP17 expression were decreased in the bulbourethral glands compared to other glands. ESR1 expression was increased in the prostate compared to the bulbourethral glands, and no differences were seen with CYP19 or 3β-HSD. In conclusion, sex steroid receptors are expressed in all equine male accessory sex glands in all stages of life, while the steroidogenic enzymes were weakly and variably expressed.