Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells

Emerging evidence suggests that sex steroids are important for human skin health. In particular, estrogen improves skin thickness, elasticity and moisture of older women. The major source of circulating estrogen is the ovary; however, local estrogen synthesis and secretion have important roles in,...

Full description

Bibliographic Details
Main Authors: Masatada Watanabe, Shuji Ohno, Hiroshi Wachi
Format: Article
Language:English
Published: Bioscientifica 2017-02-01
Series:Endocrine Connections
Subjects:
Online Access:http://www.endocrineconnections.com/content/6/2/82.full
_version_ 1811284458252271616
author Masatada Watanabe
Shuji Ohno
Hiroshi Wachi
author_facet Masatada Watanabe
Shuji Ohno
Hiroshi Wachi
author_sort Masatada Watanabe
collection DOAJ
description Emerging evidence suggests that sex steroids are important for human skin health. In particular, estrogen improves skin thickness, elasticity and moisture of older women. The major source of circulating estrogen is the ovary; however, local estrogen synthesis and secretion have important roles in, for example, bone metabolism and breast cancer development. We hypothesized that infiltrated peripheral monocytes are one of the sources of estrogen in skin tissues. We also hypothesized that, during atopic dermatitis under stress, a decline in the hypothalamus–pituitary–adrenal axis (HPA) and facilitation of the (hypothalamus)–sympathetic–adrenomedullary system (SAM) attenuates estrogen secretion from monocytes. Based on this hypothesis, we tested aromatase expression in the human peripheral monocyte-derived cell line THP-1 in response to the synthetic glucocorticoid dexamethasone (Dex), the synthetic β-agonist isoproterenol (Iso) and the β-antagonist propranolol (Pro). Dex mimics glucocorticoid secreted during excitation of the HPA, and Iso mimics catecholamine secreted during excitation of the SAM. We found that aromatase activity and the CYP19A1 gene transcript were both upregulated in THP-1 cells in the presence of Dex. Addition of Iso induced their downregulation and further addition of Pro rescued aromatase expression. These results may suggest that attenuation of estrogen secretion from peripheral monocytes could be a part of the pathology of stress-caused deterioration of atopic dermatitis. Further examination using an in vitro human skin model including THP-1 cells might be a valuable tool for investigating the therapeutic efficacy and mechanism of estrogen treatment for skin health.
first_indexed 2024-04-13T02:28:55Z
format Article
id doaj.art-e808246f68df4173ba8f4f266a1a41fb
institution Directory Open Access Journal
issn 2049-3614
2049-3614
language English
last_indexed 2024-04-13T02:28:55Z
publishDate 2017-02-01
publisher Bioscientifica
record_format Article
series Endocrine Connections
spelling doaj.art-e808246f68df4173ba8f4f266a1a41fb2022-12-22T03:06:40ZengBioscientificaEndocrine Connections2049-36142049-36142017-02-0162828810.1530/EC-16-0099Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cellsMasatada Watanabe0Shuji Ohno1Hiroshi Wachi2Laboratory of Tissue Regeneration, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Shinagawa, Tokyo, JapanDivision of Research for Pharmacy Students Education, Hoshi University, Shinagawa, Tokyo, JapanLaboratory of Tissue Regeneration, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Shinagawa, Tokyo, JapanEmerging evidence suggests that sex steroids are important for human skin health. In particular, estrogen improves skin thickness, elasticity and moisture of older women. The major source of circulating estrogen is the ovary; however, local estrogen synthesis and secretion have important roles in, for example, bone metabolism and breast cancer development. We hypothesized that infiltrated peripheral monocytes are one of the sources of estrogen in skin tissues. We also hypothesized that, during atopic dermatitis under stress, a decline in the hypothalamus–pituitary–adrenal axis (HPA) and facilitation of the (hypothalamus)–sympathetic–adrenomedullary system (SAM) attenuates estrogen secretion from monocytes. Based on this hypothesis, we tested aromatase expression in the human peripheral monocyte-derived cell line THP-1 in response to the synthetic glucocorticoid dexamethasone (Dex), the synthetic β-agonist isoproterenol (Iso) and the β-antagonist propranolol (Pro). Dex mimics glucocorticoid secreted during excitation of the HPA, and Iso mimics catecholamine secreted during excitation of the SAM. We found that aromatase activity and the CYP19A1 gene transcript were both upregulated in THP-1 cells in the presence of Dex. Addition of Iso induced their downregulation and further addition of Pro rescued aromatase expression. These results may suggest that attenuation of estrogen secretion from peripheral monocytes could be a part of the pathology of stress-caused deterioration of atopic dermatitis. Further examination using an in vitro human skin model including THP-1 cells might be a valuable tool for investigating the therapeutic efficacy and mechanism of estrogen treatment for skin health.http://www.endocrineconnections.com/content/6/2/82.fullβ-agonistaromataseatopic dermatitismonocyteestrogen
spellingShingle Masatada Watanabe
Shuji Ohno
Hiroshi Wachi
Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
Endocrine Connections
β-agonist
aromatase
atopic dermatitis
monocyte
estrogen
title Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
title_full Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
title_fullStr Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
title_full_unstemmed Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
title_short Effect of β-agonist on the dexamethasone-induced expression of aromatase by the human monocyte cells
title_sort effect of β agonist on the dexamethasone induced expression of aromatase by the human monocyte cells
topic β-agonist
aromatase
atopic dermatitis
monocyte
estrogen
url http://www.endocrineconnections.com/content/6/2/82.full
work_keys_str_mv AT masatadawatanabe effectofbagonistonthedexamethasoneinducedexpressionofaromatasebythehumanmonocytecells
AT shujiohno effectofbagonistonthedexamethasoneinducedexpressionofaromatasebythehumanmonocytecells
AT hiroshiwachi effectofbagonistonthedexamethasoneinducedexpressionofaromatasebythehumanmonocytecells