Spyroglou Ariadni, Manolopoulou Jenny, Wagner Sibylle, Bidlingmaier Martin, Reincke Martin, Beuschlein Felix
Department of Medicine, Endocrine Research, University Hospital Innenstadt, Ludwig Maximilians University, Munich, Germany.
J Mol Endocrinol. 2009 May;42(5):407-13. doi: 10.1677/JME-08-0167. Epub 2009 Feb 12.
Aldosterone is synthesized acutely from the zona glomerulosa cells upon stimulation by the renin-angiotensin-aldosterone system. Several enzymes are involved in this steroidogenic process including the steroidogenic acute regulatory protein (StAR), P450 side chain cleavage enzyme (Cyp11a1), and aldosterone synthase (Cyp11b2) which has been demonstrated to be transcriptionally regulated by the nuclear transcription factors NGF1-B and Nurr1. We investigated the short time transcriptional regulation of these genes in wild-type mice at 10 min intervals for 1 h following application of 0.2 nmol angiotensin II (ANGII) or sodium chloride in comparison sham injections. Using real-time PCR a fast upregulation of adrenal Cyp11b2 expression (53+/-5% increase over baseline) could be observed 10 min after sham injection which was accompanied by a transient increase in aldosterone secretion while StAR and Cyp11a1 upregulation was delayed and more sustained. ANGII caused an increase of StAR and Cyp11a1 expression similar to that observed after sham injection while Cyp11b2 upregulation was more pronounced (10 min, 236+/-39%) and reflected ANGII induced stimulation of aldosterone output. Sodium challenge was followed by a sustained reduction of all three genes examined (Cyp11b2, 20 min, -63+/-6%) which was accompanied by a significant suppression of aldosterone secretion detectable after 60 min. While increases in NGF1-B mRNA levels were similar between the treatment groups, Nurr1 expression levels were induced only upon ANGII administration. These data suggest that acute regulation of aldosterone synthesis is accompanied by fast transcriptional modulation of steroidogenic enzymes and transcription factors that are likely to be involved in aldosterone secretion.
醛固酮是在肾素 - 血管紧张素 - 醛固酮系统的刺激下,由球状带细胞急性合成的。几种酶参与了这个类固醇生成过程,包括类固醇生成急性调节蛋白(StAR)、P450侧链裂解酶(Cyp11a1)和醛固酮合酶(Cyp11b2),后者已被证明受核转录因子NGF1 - B和Nurr1的转录调控。我们研究了在野生型小鼠中,与假注射相比,在注射0.2 nmol血管紧张素II(ANGII)或氯化钠后1小时内,每隔10分钟这些基因的短期转录调控情况。使用实时PCR,在假注射后10分钟可观察到肾上腺Cyp11b2表达快速上调(比基线增加53±5%),同时醛固酮分泌短暂增加,而StAR和Cyp11a1的上调延迟且更持久。ANGII导致StAR和Cyp11a1表达增加,与假注射后观察到的情况相似,而Cyp11b2的上调更明显(10分钟时为236±39%),反映了ANGII诱导的醛固酮产量增加。钠刺激后,所检测的所有三个基因(Cyp11b2,20分钟时为-63±6%)持续减少,60分钟后可检测到醛固酮分泌显著受到抑制。虽然各治疗组之间NGF1 - B mRNA水平的增加相似,但仅在给予ANGII后诱导Nurr1表达水平。这些数据表明,醛固酮合成的急性调节伴随着类固醇生成酶和转录因子的快速转录调节,这些因子可能参与醛固酮分泌。