Item Type: | Article |
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Title: | Transforming growth factor β1 inhibits aldosterone and cortisol production in the human adrenocortical cell line NCI-H295R through inhibition of CYP11B1 and CYP11B2 expression |
Creators Name: | Liakos, P., Lenz, D., Bernhardt, R., Feige, J.J. and Defaye, G. |
Abstract: | Transforming growth factor {beta}1 (TGF{beta}1) has been shown to exert strong inhibitory effects on adrenocortical cell steroidogenesis. However, the molecular targets of TGF{beta}1 in adrenocortical cells appear to differ between species. Here, we report the first characterization of the regulatory effects of TGF{beta}1 on the steroidogenic functions of the human adrenocortical tumor cell line NCI-H295R. After treatment with 2 ng/ml TGF{beta}1 for 24 h, basal production of corticosterone, cortisol and androstenedione was dramatically decreased. When TGF{beta}1 was added simultaneously with forskolin, the production of cortisol and 11-hydroxyandrostenedione was decreased by 85% whereas that of deoxycortisol was increased. When TGF{beta}1 was added simultaneously with angiotensin II, aldosterone production was reduced by 80%. We observed that TGF{beta}1 strongly inhibits forskolin-induced steroid 11{beta}-hydroxylase activity and CYP11B1 mRNA levels, as well as angiotensin II-induced aldosterone synthase activity and CYP11B2 mRNA levels. CYP11B1 and CYP11B2 gene products thus appear as the major steroidogenic enzymes down-regulated by TGF{beta}1 in the human adrenocortical tumor cell line NCI-H295R. |
Keywords: | Adrenal Cortex, Adrenocorticotropic Hormone, Aldosterone, Aldosterone Synthase, Analysis of Variance, Androstenedione, Angiotensin II, Chemical Depression, Corticosterone, Cortodoxone, Cultured Tumor Cells, Forskolin, Hydrocortisone, Messenger RNA, Teroid 11-Beta-Hydroxylase, Transforming Growth Factor Beta |
Source: | Journal of Endocrinology |
ISSN: | 0022-0795 |
Publisher: | Society for Endocrinology |
Volume: | 176 |
Number: | 1 |
Page Range: | 69-82 |
Date: | 1 January 2003 |
Official Publication: | https://doi.org/10.1677/joe.0.1760069 |
PubMed: | View item in PubMed |
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