Evidence of sexual dimorphism in placental vitamin D metabolism: Testosterone inhibits calcitriol-dependent cathelicidin expression. Issue 163 (October 2016)

• Record Type: Journal Article
• Authors: Olmos-Ortiz, Andrea; García-Quiroz, Janice; López-Marure, Rebeca; González-Curiel, Irma; Rivas-Santiago, Bruno; Olivares, Aleida; Avila, Euclides; Barrera, David; Halhali, Ali; Caldiño, Felipe; Larrea, Fernando; Díaz, Lorenza
• Is Part Of: Journal of steroid biochemistry and molecular biology. Issue 163(2016)
• Page Start: 173
• Page End: 182
• Publication Date: 2016-10
• Subjects: 25OHD3 25-hydroxyvitamin D3 -- AR Androgen Receptor -- cAMP cyclic AMP -- CRE cAMP response elements -- CREB cAMP response element binding protein -- DHT 5α-dihydrotestosterone -- E2 17β-estradiol -- hCTD human Cathelicidin -- VD vitamin D -- VDR vitamin D receptor; LL-37 -- Cord blood -- Male -- cAMP -- Androgen; Steroid hormones -- Periodicals; Biochemistry -- Periodicals; Hormones -- Periodicals; Molecular Biology -- Periodicals; Hormones stéroïdes -- Périodiques; Steroid hormones; Periodicals; 572.579
• DOI: 10.1016/j.jsbmb.2016.05.017
• Languages: English
• ISSNs: 0960-0760

Abstract

Graphical abstract: Highlights: Testosterone stimulates CYP24A1and inhibits CYP27B1 placental gene expression. Testosterone phosphorylates CREB in a cAMP independent and AR dependent manner. The placental VD-dependent expression of hCTD is reduced by androgen exposure. Male placental cotyledons express less CYP27B1 and hCTD mRNA compared to females. Male newborns had lower serum umbilical cord hCTD concentration compared to females. Abstract: Male fetus and neonates show increased immune vulnerability compared to females, which results in a higher risk of perinatal infections. These differences could partially be due to sex steroids differential modulation of vitamin D metabolism; since calcitriol, the most active vitamin D metabolite, regulates immune responses and transcriptionally induces the antimicrobial peptide cathelicidin in the human placenta. Calcitriol availability depends on CYP27B1 and CYP24A1 expression, the cytochromes involved in its synthesis and degradation, respectively. However, the effects of testosterone upon these enzymes and the final biological outcome upon the calcitriol-dependent immune-target cathelicidin in the placenta have not been studied. In this study we show that testosterone significantly inhibited CYP27B1 while stimulated CYP24A1 gene expression in cultured trophoblasts. These effects were accompanied by CREB activation through cAMP–independent and androgen receptor-dependent mechanisms. Male placental cotyledons showed reduced basal CYP27B1 and cathelicidin gene expression compared to females ( P < 0.05). Testosterone concentration was higher in the cord blood of male neonates ( P = 0.007), whereas cathelicidin levels were lesser compared to females ( P = 0.002). Altogether our results suggest that male placentas produce less cathelicidin due to decreased calcitriol bioavailability. We propose that the observed sex-dependent differences in placental vitamin D metabolism contribute in fetal responses to infections and could partially explain why the increased male fetuses immune vulnerability. Moreover, gestational hyperandrogenemia could adversely affect placental vitamin D metabolism independently of fetal sex.