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异常促性腺激素释放激素受体(GnRHR)表达及其对肾上腺醛固酮分泌腺瘤(APA)中CYP11B2表达和醛固酮生成的调节作用。

Aberrant gonadotropin-releasing hormone receptor (GnRHR) expression and its regulation of CYP11B2 expression and aldosterone production in adrenal aldosterone-producing adenoma (APA).

作者信息

Nakamura Yasuhiro, Hattangady Namita G, Ye Ping, Satoh Fumitoshi, Morimoto Ryo, Ito-Saito Takako, Sugawara Akira, Ohba Koji, Takahashi Kazuhiro, Rainey William E, Sasano Hironobu

机构信息

Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.

Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, United States; Department of Physiology, Georgia Regents University, Augusta, GA, United States.

出版信息

Mol Cell Endocrinol. 2014 Mar 25;384(1-2):102-8. doi: 10.1016/j.mce.2014.01.016. Epub 2014 Jan 25.

Abstract

Aberrant expression of gonadotropin-releasing hormone receptor (GnRHR) has been reported in human adrenal tissues including aldosterone-producing adenoma (APA). However, the details of its expression and functional role in adrenals are still not clear. In this study, quantitative RT-PCR analysis revealed the mean level of GnRHR mRNA was significantly higher in APAs than in human normal adrenal (NA) (P=0.004). GnRHR protein expression was detected in human NA and neoplastic adrenal tissues. In H295R cells transfected with GnRHR, treatment with GnRH resulted in a concentration-dependent increase in CYP11B2 reporter activity. Chronic activation of GnRHR with GnRH (100nM), in a cell line with doxycycline-inducible GnRHR (H295R-TR/GnRHR), increased CYP11B2 expression and aldosterone production. These agonistic effects were inhibited by blockers for the calcium signaling pathway, KN93 and calmidazolium. These results suggest GnRH, through heterotopic expression of its receptor, may be a potential regulator of CYP11B2 expression levels in some cases of APA.

摘要

据报道,促性腺激素释放激素受体(GnRHR)在包括醛固酮瘤(APA)在内的人类肾上腺组织中存在异常表达。然而,其在肾上腺中的表达细节和功能作用仍不清楚。在本研究中,定量逆转录聚合酶链反应(RT-PCR)分析显示,APA中GnRHR信使核糖核酸(mRNA)的平均水平显著高于正常人类肾上腺(NA)(P = 0.004)。在人类NA和肾上腺肿瘤组织中检测到了GnRHR蛋白表达。在用GnRHR转染的H295R细胞中,用促性腺激素释放激素(GnRH)处理导致细胞色素P450 11B2(CYP11B2)报告基因活性呈浓度依赖性增加。在具有强力霉素诱导型GnRHR的细胞系(H295R-TR/GnRHR)中,用GnRH(100纳摩尔)长期激活GnRHR可增加CYP11B2表达和醛固酮生成。钙信号通路阻滞剂KN93和氯米达唑可抑制这些激动效应。这些结果表明,GnRH通过其受体的异位表达,在某些APA病例中可能是CYP11B2表达水平的潜在调节因子。

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