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Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity

The pituitary hormone prolactin (PRL), originally described for its role in lactation, has been implemented in over 300 functions and is produced by multiple cell types outside of the pituitary. Monocyte/macrophages in particular show robust expression of extra-pituitary prolactin (ePRL). While ePRL...

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Autores principales: Barrett, Richard, Narasimhulu, Chandrakala Aluganti, Parthasarathy, Sampath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792634/
https://www.ncbi.nlm.nih.gov/pubmed/29386559
http://dx.doi.org/10.1038/s41598-018-20378-1
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author Barrett, Richard
Narasimhulu, Chandrakala Aluganti
Parthasarathy, Sampath
author_facet Barrett, Richard
Narasimhulu, Chandrakala Aluganti
Parthasarathy, Sampath
author_sort Barrett, Richard
collection PubMed
description The pituitary hormone prolactin (PRL), originally described for its role in lactation, has been implemented in over 300 functions and is produced by multiple cell types outside of the pituitary. Monocyte/macrophages in particular show robust expression of extra-pituitary prolactin (ePRL). While ePRL protein is identical to pituitary PRL and translated from the same gene, tissues outside the pituitary engage an alternative promoter to regulate expression. Many of the factors regulating this expression, however, remain unknown. Here we show that the adrenergic hormones epinephrine and norepinephrine induce PRL expression in the human monocytic cell line THP-1 at physiological concentrations. Furthermore, our experiments show the polarization state of differentiated macrophages can influence their response in vitro, with inflammatory M(1) macrophages—common in obese adipose—showing the highest levels of PRL expression compared to other macrophage types. Adrenergic hormones have a clearly defined role in adipocyte lipid metabolism, stimulating lipolysis through hormone sensitive lipase (HSL) induction. Meanwhile, PRL has been shown to stimulate lipogenesis. This highlights ePRL production as a possible factor in obesity. The overall balance of these two signals could play a critical role in determining overall lipid turnover/accumulation in adipose depots where large numbers of adipose tissue macrophages (ATMs) reside.
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spelling pubmed-57926342018-02-12 Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity Barrett, Richard Narasimhulu, Chandrakala Aluganti Parthasarathy, Sampath Sci Rep Article The pituitary hormone prolactin (PRL), originally described for its role in lactation, has been implemented in over 300 functions and is produced by multiple cell types outside of the pituitary. Monocyte/macrophages in particular show robust expression of extra-pituitary prolactin (ePRL). While ePRL protein is identical to pituitary PRL and translated from the same gene, tissues outside the pituitary engage an alternative promoter to regulate expression. Many of the factors regulating this expression, however, remain unknown. Here we show that the adrenergic hormones epinephrine and norepinephrine induce PRL expression in the human monocytic cell line THP-1 at physiological concentrations. Furthermore, our experiments show the polarization state of differentiated macrophages can influence their response in vitro, with inflammatory M(1) macrophages—common in obese adipose—showing the highest levels of PRL expression compared to other macrophage types. Adrenergic hormones have a clearly defined role in adipocyte lipid metabolism, stimulating lipolysis through hormone sensitive lipase (HSL) induction. Meanwhile, PRL has been shown to stimulate lipogenesis. This highlights ePRL production as a possible factor in obesity. The overall balance of these two signals could play a critical role in determining overall lipid turnover/accumulation in adipose depots where large numbers of adipose tissue macrophages (ATMs) reside. Nature Publishing Group UK 2018-01-31 /pmc/articles/PMC5792634/ /pubmed/29386559 http://dx.doi.org/10.1038/s41598-018-20378-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barrett, Richard
Narasimhulu, Chandrakala Aluganti
Parthasarathy, Sampath
Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title_full Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title_fullStr Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title_full_unstemmed Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title_short Adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
title_sort adrenergic hormones induce extrapituitary prolactin gene expression in leukocytes-potential implications in obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792634/
https://www.ncbi.nlm.nih.gov/pubmed/29386559
http://dx.doi.org/10.1038/s41598-018-20378-1
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