Mammary gland-specific regulation of GNRH and GNRH-receptor gene expression is likely part of a local autoregulatory system in female vizcachas (Rodentia: Chinchillidae)

•GNRH and GNRHR are transcribed in mammary glands of vizcachas throughout pregnancy and lactation.•GNRH and GNRHR are expressed in the secretory epithelia of alveoli and ducts.•GNRH is released to the alveolus lumen as a component of milk during lactation.•Variations in pituitary prolactin levels in...

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Veröffentlicht in:General and comparative endocrinology 2020-09, Vol.296, p.113518, Article 113518
Hauptverfasser: Corso, María Clara, Cortasa, Santiago Andrés, Schmidt, Alejandro Raúl, Proietto, Sofía, Inserra, Pablo Ignacio Felipe, Fernández, Marina Olga, Di Giorgio, Noelia, Lux-Lantos, Victoria, Vitullo, Alfredo Daniel, Dorfman, Verónica Berta, Halperin, Julia
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Sprache:eng
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Zusammenfassung:•GNRH and GNRHR are transcribed in mammary glands of vizcachas throughout pregnancy and lactation.•GNRH and GNRHR are expressed in the secretory epithelia of alveoli and ducts.•GNRH is released to the alveolus lumen as a component of milk during lactation.•Variations in pituitary prolactin levels induce changes in the content of mammary GNRH.•GNRH induces its own transcription and that of EGR1 suggesting a positive feedback mechanism in mammary glands. In addition to key mammotrophic hormones such as the pituitary prolactin (PRL) and the ovarian steroids progesterone and estradiol, there are local factors that modulate the tissue dynamics of the mammary glands during pregnancy and lactation. By immunohistochemistry and RT-PCR, we found local transcription and translation of gonadotropin-releasing hormone (GNRH), GNRH receptor (GNRHR), PRL and PRL receptor (PRLR) in mammary glands of adult vizcachas during pregnancy and lactation. Both GNRH and GNRHR showed a lag between protein expression and gene transcription throughout the gestational period: while the highest transcription levels of these genes were recorded at early-pregnancy, the epithelial immunoexpressions of both showed their maximum during lactation. RIA results corroborated the presence of GNRH in mammary glands at all the analyzed stages and confirmed the maximum amount of this peptide in the lactating group. Significant amounts of GNRH were detected in milk samples as well. Conversely, PRL and PRLR shared similar protein and gene expression profiles, all exhibiting maximum values during lactation. GNRH peptide content in mammary glands of females with sulpiride-induced hyperprolactinemia (HP) was significantly lower than that of control females (CT). Although PRL mRNA levels remained unchanged, there was a marked increase in theα-lactalbumin (LALBA) transcription in mammary glands of HP- vs CT-females. These results suggest that after targeting mammary glands, PRL stimulates the expression of milk protein genes, but also, tempers the local expression of GNRH. Mammary gland-explantssupplemented with a GNRH analogue (GN-explants) had no differences in terms of PRLR orLALBA transcription levels compared to CT-explants, so the mammary PRLR signaling would not appear to be modulated by GNRH. Yet, mRNA expression levels of both GNRH and the GNRHR-downstream factor, EGR1, were significantly higher in GN-explants compared to that of CT which would point to a GNRH-positive feedback mechanism. In summar
ISSN:0016-6480
1095-6840
DOI:10.1016/j.ygcen.2020.113518