Romero Damian G, Zhou Ming Yi, Yanes Licy L, Plonczynski Maria W, Washington Tanganika R, Gomez-Sanchez Celso E, Gomez-Sanchez Elise P
Division of Endocrinology, G V (Sonny) Montgomery VA Medical Center, and Department of Medicine, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA.
J Endocrinol. 2007 Aug;194(2):429-40. doi: 10.1677/JOE-07-0153.
Regulators of G-protein signaling (RGS proteins) interact with Galpha subunits of heterotrimeric G-proteins, accelerating the rate of GTP hydrolysis and finalizing the intracellular signaling triggered by the G-protein-coupled receptor (GPCR)-ligand interaction. Angiotensin II (Ang II) interacts with its GPCR in adrenal zona glomerulosa cells and triggers a cascade of intracellular signals that regulates steroidogenesis and proliferation. On screening for adrenal zona glomerulosa-specific genes, we found that RGS4 was exclusively localized in the zona glomerulosa of the rat adrenal cortex. We studied RGS4 expression and regulation in the rat adrenal gland, including the signaling pathways involved, as well as the role of RGS4 in steroidogenesis in human adrenocortical H295R cells. We reported that RGS4 mRNA expression in the rat adrenal gland was restricted to the adrenal zonal glomerulosa and upregulated by low-salt diet and Ang II infusion in rat adrenal glands in vivo. In H295R cells, Ang II caused a rapid and transient increase in RGS4 mRNA levels mediated by the calcium/calmodulin/calmodulin-dependent protein kinase and protein kinase C pathways. RGS4 overexpression by retroviral infection in H295R cells decreased Ang II-stimulated aldosterone secretion. In reporter assays, RGS4 decreased Ang II-mediated aldosterone synthase upregulation. In summary, RGS4 is an adrenal gland zona glomerulosa-specific gene that is upregulated by aldosterone secretagogues, in vivo and in vitro, and functions as a negative feedback of Ang II-triggered intracellular signaling. Alterations in RGS4 expression levels or functions may be involved in deregulations of Ang II signaling and abnormal aldosterone secretion.
G蛋白信号调节因子(RGS蛋白)与异源三聚体G蛋白的Gα亚基相互作用,加快GTP水解速率,并终止由G蛋白偶联受体(GPCR)-配体相互作用触发的细胞内信号传导。血管紧张素II(Ang II)与其在肾上腺球状带细胞中的GPCR相互作用,并触发一系列调节类固醇生成和增殖的细胞内信号。在筛选肾上腺球状带特异性基因时,我们发现RGS4仅定位在大鼠肾上腺皮质的球状带。我们研究了RGS4在大鼠肾上腺中的表达和调节,包括涉及的信号通路,以及RGS4在人肾上腺皮质H295R细胞类固醇生成中的作用。我们报道,大鼠肾上腺中RGS4 mRNA的表达仅限于肾上腺球状带,并且在体内通过低盐饮食和向大鼠肾上腺中注射Ang II而上调。在H295R细胞中,Ang II通过钙/钙调蛋白/钙调蛋白依赖性蛋白激酶和蛋白激酶C途径介导RGS4 mRNA水平的快速短暂升高。通过逆转录病毒感染在H295R细胞中过表达RGS4可降低Ang II刺激的醛固酮分泌。在报告基因分析中,RGS4降低了Ang II介导的醛固酮合酶上调。总之,RGS4是一种肾上腺球状带特异性基因,在体内和体外均受醛固酮分泌刺激物上调,并作为Ang II触发的细胞内信号的负反馈。RGS4表达水平或功能的改变可能与Ang II信号传导失调和醛固酮分泌异常有关。