Eason M G, Liggett S B
Department of Medicine (Pulmonary), University of Cincinnati College of Medicine, OH 45267.
Biochem Biophys Res Commun. 1993 May 28;193(1):318-23. doi: 10.1006/bbrc.1993.1626.
Recently it has become clear that alpha 2-adrenergic receptors (alpha 2AR) functionally couple to Gs as well as Gi, thus inducing a complex modulation of adenylyl cyclase activity. It is unknown whether alpha 2AR-Gs coupling undergoes agonist-promoted desensitization. Therefore, in CHO cells expressing the three cloned human alpha 2AR subtypes (alpha 2C10, alpha 2C4, and alpha 2C2), we assessed the ability of alpha 2AR-mediated stimulation of adenylyl cyclase activity to undergo short-term agonist-promoted desensitization. To isolate alpha 2AR-Gs coupling, cells were pretreated with pertussis toxin, which ablates Gi coupling. Following agonist exposure, both alpha 2C10- and alpha 2C2-mediated stimulation of adenylyl cyclase activity underwent marked desensitization. In distinct contrast, alpha 2C4-mediated stimulation of adenylyl cyclase activity underwent no agonist-promoted desensitization. Thus, alpha 2AR-Gs coupling undergoes agonist-promoted desensitization and does so in a subtype-selective manner.
最近已明确,α2 - 肾上腺素能受体(α2AR)在功能上可与Gs以及Gi偶联,从而对腺苷酸环化酶活性产生复杂的调节作用。目前尚不清楚α2AR - Gs偶联是否会发生激动剂促进的脱敏作用。因此,在表达三种克隆的人α2AR亚型(α2C10、α2C4和α2C2)的CHO细胞中,我们评估了α2AR介导的腺苷酸环化酶活性刺激发生短期激动剂促进的脱敏作用的能力。为了分离α2AR - Gs偶联,细胞先用百日咳毒素预处理,以消除Gi偶联。在激动剂暴露后,α2C10和α2C2介导的腺苷酸环化酶活性刺激均发生了明显的脱敏作用。与之形成鲜明对比的是,α2C4介导的腺苷酸环化酶活性刺激未发生激动剂促进的脱敏作用。因此,α2AR - Gs偶联会发生激动剂促进的脱敏作用,并且是以亚型选择性的方式进行的。