Effect of 2,2 ',4,4 '-tetrahydroxybenzophenone (BP2) on steroidogenesis in testicular Leydig cells

Authors
Kim, YeawonRyu, Jae ChunChoi, Hueng-SikLee, Keesook
Issue Date
2011-10-09
Publisher
ELSEVIER IRELAND LTD
Citation
TOXICOLOGY, v.288, no.1-3, pp.18 - 26
Abstract
Endocrine disruptors (EDs) affect the function of animal reproductive systems. Recently, 2,2',4,4'-tetrahydroxybenzophenone (BP2), which is a component of UV protection products, was found to be an ED that interferes with the thyroid hormone (TH) axis. However, BP2 activity in the testis has not been well addressed. In this study, we have examined the effects of BP2 on steroidogenesis in testicular Leydig cells in connection with thyroid hormone signaling, which is known to play an important role in testicular development and function. Our study showed that 8P2 affected the expression of steroidogenic enzyme genes in testicular Leydig cells, which is differentially regulated by thyroid hormone/thyroid hormone receptor (TR) signaling. In MA-10 Leydig cell line, TR/T3 signaling increased the expression of P450c17 and P450scc, while it decreased the expression of StAR and 3 beta-HSD. Interestingly, BP2 affected the expression of steroidogenic enzyme genes in a manner opposite to that of T3 signaling. BP2 downregulated the TR alpha/T3-activation of P450c17 and P450scc expression while enhancing the TR alpha/T3-repression of StAR and 3 beta-HSD expression. Transient transfection analyses with promoter-reporter constructs revealed that BP2 altered the expression of steroidogenic enzyme genes by affecting the cAMP and Nur77-activated promoter activity of P450c17, StAR, and 3 beta-HSD. Animal experiments with mice revealed that BP2 decreased the production of testosterone in the testis by affecting the expression of some steroidogenic enzyme genes in vivo. Together, these findings elucidate a molecular mechanism of BP2 action underlying testicular steroidogenesis and also suggest that BP2 acts, in part, as a thyroid antagonist that affects steroidogenesis in the testis. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
Keywords
THYROID-HORMONE RECEPTORS; IN-VITRO; BENZOPHENONE-2 BP2; NUCLEAR RECEPTORS; UV FILTERS; EXPRESSION; RAT; MECHANISMS; HYPOTHYROIDISM; TRANSCRIPTION; THYROID-HORMONE RECEPTORS; IN-VITRO; BENZOPHENONE-2 BP2; NUCLEAR RECEPTORS; UV FILTERS; EXPRESSION; RAT; MECHANISMS; HYPOTHYROIDISM; TRANSCRIPTION; BP2; Endocrine disruptors (EDs); Thyroid hormone receptor/T3 signaling; Testis; Gene regulation
ISSN
0300-483X
URI
https://pubs.kist.re.kr/handle/201004/129896
DOI
10.1016/j.tox.2011.06.013
Appears in Collections:
KIST Article > 2011
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