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

机译:肾上腺醛固酮生成腺瘤(APA)中异常促性腺激素释放激素受体(GnRHR)的表达及其对CYP11B2表达和醛固酮生成的调节

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摘要

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 (100 nM), 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.
机译:促性腺激素释放激素受体(GnRHR)的异常表达已在人的肾上腺组织(包括生产醛固酮的腺瘤(APA))中报道。但是,其在肾上腺中的表达和功能作用的细节仍不清楚。在这项研究中,定量RT-PCR分析显示,APA中GnRHR mRNA的平均水平显着高于人正常肾上腺(NA)(P = 0.004)。在人NA和赘生性肾上腺组织中检测到GnRHR蛋白表达。在用GnRHR转染的H295R细胞中,用GnRH处理导致CYP11B2报告基因活性呈浓度依赖性增加。在具有强力霉素诱导的GnRHR(H295R-TR / GnRHR)的细胞系中,用GnRH(100 nM)长期激活GnRHR,增加CYP11B2的表达和醛固酮的产生。这些激动作用被钙信号传导通路,KN93和卡地咪唑的阻滞剂抑制。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剂。

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