Chen Yung-Chia, Huang Shih-Horng, Wang Seu-Mei
Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, and Far Eastern Memorial Hospital, Department of Surgery and Division of General Surgery, Taipei 100, Taiwan.
Int J Biochem Cell Biol. 2008;40(12):2815-25. doi: 10.1016/j.biocel.2008.05.016. Epub 2008 Jun 5.
Adenosine promotes adrenal steroidogenesis in vitro and in vivo. However, the underlying signaling mechanisms of this event and the function of the adenosine receptor subtypes in adrenal cells remain to be elucidated. Expression of A1, A2A, A2B, and A3 adenosine receptor mRNA in rat adrenal cells was shown by reverse transcription-polymerase chain reaction. Adenosine increased corticosterone production in a time- and dose-dependent manner, and this adenosine effect was mediated by the A2 adenosine receptors, since the antagonists specific for the A2A and A2B adenosine receptors, and specific silencing the A2A adenosine receptor expression with small interfering RNA significantly blocked the adenosine-induced steroidogenesis. Using pharmacological approaches, we further demonstrated that Janus kinase 2 was the downstream molecule next to the A2A and A2B adenosine receptors. Inhibition of Janus kinase 2 prevented the adenosine-induced steroidogenesis and phosphorylation of mitogen-activated protein kinase kinase 1/2 and extracellular signal-regulated kinase 1/2, demonstrating that Janus kinase 2 was the upstream effector of the mitogen-activated protein kinase kinase pathway. Pretreatment with A2 adenosine receptor, Janus kinase 2, or mitogen-activated protein kinase kinase inhibitors significantly decreased the adenosine-induced phosphorylation of 3',5'-cyclic adenosine monophosphate responsive element binding protein. In conclusion, these data show that adenosine-stimulated steroidogenesis is mediated via the A2A and A2B adenosine receptors, activation of which triggers the Janus kinase 2-mitogen-activated protein kinase kinase-extracellular signal-regulated kinase cascade and 3',5'-cyclic adenosine monophosphate responsive element binding protein phosphorylation. Based on its stimulatory effect on glucocorticoid production, adenosine is a potential candidate as anti-inflammatory agent.
腺苷在体外和体内均能促进肾上腺类固醇生成。然而,这一过程的潜在信号传导机制以及肾上腺细胞中腺苷受体亚型的功能仍有待阐明。通过逆转录-聚合酶链反应显示了大鼠肾上腺细胞中A1、A2A、A2B和A3腺苷受体mRNA的表达。腺苷以时间和剂量依赖性方式增加皮质酮的产生,并且这种腺苷效应是由A2腺苷受体介导的,因为A2A和A2B腺苷受体的特异性拮抗剂以及用小干扰RNA特异性沉默A2A腺苷受体表达可显著阻断腺苷诱导的类固醇生成。使用药理学方法,我们进一步证明Janus激酶2是A2A和A2B腺苷受体下游的分子。抑制Janus激酶2可阻止腺苷诱导的类固醇生成以及丝裂原活化蛋白激酶激酶1/2和细胞外信号调节激酶1/2的磷酸化,表明Janus激酶2是丝裂原活化蛋白激酶激酶途径的上游效应器。用A2腺苷受体、Janus激酶2或丝裂原活化蛋白激酶激酶抑制剂预处理可显著降低腺苷诱导的3',5'-环磷酸腺苷反应元件结合蛋白的磷酸化。总之,这些数据表明,腺苷刺激的类固醇生成是通过A2A和A2B腺苷受体介导的,其激活触发Janus激酶2-丝裂原活化蛋白激酶激酶-细胞外信号调节激酶级联反应以及3',5'-环磷酸腺苷反应元件结合蛋白磷酸化。基于其对糖皮质激素产生的刺激作用,腺苷是一种潜在的抗炎剂候选物。