Department of Endocrinology, Chinese PLA General Hospital, Beijing, China.
J Endocrinol Invest. 2011 Oct;34(9):671-5. doi: 10.3275/7413.
Aldosterone synthase (CYP11B2) is responsible for the final step in aldosterone synthesis and is importantly regulated by angiotensin-II (Ang II) through diverse pathways. However, under pathological conditions, such as in hyperaldosteronism, the regulation becomes disordered. The transcription factor steroidogenic factor-1 (SF-1) is important in regulating the endocrine system and is overexpressed in aldosterone-producing adenoma (APA), a common cause of hyperaldosteronism. Overexpression of SF-1 has been extensively studied, but little in-depth information is available regarding the effects of inhibitory SF-1 on CYP11B2 and Ang II. In this paper, we have investigated the roles of down-regulated SF-1 in basal and Ang II-induced CYP11B2 expression using SF-1-specific short hairpin RNA. Inhibitory SF-1 was found to decrease the sensitivity of CYP11B2 and aldosterone to Ang II stimulation, whereas a down-regulation of SF-1 enhanced basal CYP11B2 expression and aldosterone production in H295R cells. Considering these differential effects of SF-1 on aldosterone production, these results might provide a new insight into the understanding of hyperaldosteronism.
醛固酮合酶(CYP11B2)负责醛固酮合成的最后一步,并且重要的是通过多种途径受血管紧张素-II(Ang II)调节。然而,在病理条件下,如在醛固酮增多症中,这种调节变得紊乱。转录因子类固醇生成因子-1(SF-1)在调节内分泌系统中很重要,并且在醛固酮产生腺瘤(APA)中过度表达,APA 是醛固酮增多症的常见原因。SF-1 的过表达已经被广泛研究,但是关于抑制 SF-1 对 CYP11B2 和 Ang II 的影响的深入信息很少。在本文中,我们使用 SF-1 特异性短发夹 RNA 研究了下调的 SF-1 在基础和 Ang II 诱导的 CYP11B2 表达中的作用。发现抑制性 SF-1 降低了 CYP11B2 和醛固酮对 Ang II 刺激的敏感性,而 SF-1 的下调增强了 H295R 细胞中基础 CYP11B2 的表达和醛固酮的产生。考虑到 SF-1 对醛固酮产生的这些差异作用,这些结果可能为理解醛固酮增多症提供新的见解。