Department of Internal Medicine, Rotterdam, The Netherlands.
Endocrinology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
J Endocrinol. 2020 Apr;245(1):101-113. doi: 10.1530/JOE-19-0311.
Pituitary-directed medical treatment for Cushing's disease (CD) is currently represented by membrane receptor targeting drugs (somatostatin analogs and dopamine agonists). Somatostatin and dopamine receptors are regulated by β-arrestins, which have been shown to be differentially regulated by glucocorticoids in non-neuroendocrine cells. In this study we investigated the effects of glucocorticoids on β-arrestin expression in corticotroph tumor cells. First, AtT20 cells, a mouse model of CD, were exposed to dexamethasone (Dex) at different time points and β-arrestin expression was evaluated at mRNA and protein levels. Futhermore, β-arrestin mRNA expression was evaluated in 17 human corticotroph adenoma samples and correlated to patients' pre-operative cortisol levels. We observed that Dex treatment induced a time-dependent increase in β-arrestin 1 mRNA expression and a decrease in β-arrestin 2. The same modulation pattern was observed at protein level. Dex-mediated modulation of β-arrestins was abolished by co-treatment with mifepristone, and Dex withdrawal restored β-arrestin expression to basal levels after 72 h. The evaluation of β-arrestin mRNA in corticotroph adenomas from CD patients with variable disease activity showed a significant positive correlation between β-arrestin 1 mRNA and urinary cortisol levels. The effect of glucocorticoids on β-arrestin levels was confirmed by the analysis of two samples from a single patient, which underwent adenomectomy twice, with different pre-operative cortisol levels. In conclusion, glucocorticoids induce an inverse modulation of the two β-arrestin isofoms in corticotroph tumor cells. Since β-arrestins regulate membrane receptor functions, this finding may help to better understand the variable response to pituitary-targeting drugs in patients with Cushing's disease.
库欣病(CD)的垂体定向药物治疗目前代表为膜受体靶向药物(生长抑素类似物和多巴胺激动剂)。生长抑素和多巴胺受体受β-arrestin 调节,在非神经内分泌细胞中,糖皮质激素已被证明对其有差异调节作用。在这项研究中,我们研究了糖皮质激素对促肾上腺皮质激素肿瘤细胞中β-arrestin 表达的影响。首先,将 AtT20 细胞(CD 的小鼠模型)暴露于不同时间点的地塞米松(Dex),并在 mRNA 和蛋白质水平上评估β-arrestin 表达。此外,还评估了 17 个人类促肾上腺皮质激素腺瘤样本中的β-arrestin mRNA 表达,并将其与患者术前皮质醇水平相关联。我们观察到,Dex 处理诱导β-arrestin 1 mRNA 表达的时间依赖性增加和β-arrestin 2 的减少。在蛋白质水平上观察到相同的调节模式。Dex 介导的β-arrestin 调节作用通过与米非司酮共同处理而被废除,并且 Dex 撤回后在 72 小时后将β-arrestin 表达恢复到基础水平。对 CD 患者具有不同疾病活性的促肾上腺皮质激素腺瘤中β-arrestin mRNA 的评估显示,β-arrestin 1 mRNA 与尿皮质醇水平之间存在显著正相关。对单个患者的两个样本的分析证实了糖皮质激素对β-arrestin 水平的影响,该患者接受了两次腺瘤切除术,术前皮质醇水平不同。总之,糖皮质激素诱导促肾上腺皮质激素肿瘤细胞中两种β-arrestin 同种型的反向调节。由于β-arrestin 调节膜受体功能,这一发现可能有助于更好地理解库欣病患者对垂体靶向药物的可变反应。