Rozenfeld Raphael, Devi Lakshmi A
Department of Pharmacology and Biological Chemistry, Mt. Sinai School of Medicine, One Gustave L. Levy Pl., New York, NY 10029, USA.
FASEB J. 2007 Aug;21(10):2455-65. doi: 10.1096/fj.06-7793com. Epub 2007 Mar 23.
Opiates are analgesics of choice in the treatment of chronic pain, but their long-term use leads to the development of physiological tolerance. Thus, understanding the mechanisms modulating the response of their receptor, the mu opioid receptor (muOR), is of great clinical relevance. Here we show that heterodimerization of muOR with delta opioid receptors (deltaOR) leads to a constitutive recruitment of beta-arrestin2 to the receptor complex resulting in changes in the spatio-temporal regulation of ERK1/2 signaling. The involvement of beta-arrestin2 is further supported by studies using beta-arrestin2 siRNA in cells endogenously expressing the heterodimers. The association of beta-arrestin2 with the heterodimer can be altered by treatment with a combination of muOR agonist (DAMGO) and deltaOR antagonist (Tipp(psi)), and this leads to a shift in the pattern of ERK1/2 phosphorylation to the pattern observed with muOR alone. These data indicate that, in the naive state, muOR-deltaOR heterodimers are in a conformation conducive to beta-arrestin-mediated signaling. Destabilization of this conformation by cotreatment with muOR and deltaOR ligands leads to a switch to a non-beta-arrestin-mediated signaling. Taken together, these results show for the first time that muOR-deltaOR heterodimers, by differentially recruiting beta-arrestin, modulate the spatio-temporal dynamics of opioid receptor signaling.
阿片类药物是治疗慢性疼痛的首选镇痛药,但其长期使用会导致生理耐受性的产生。因此,了解调节其受体——μ阿片受体(muOR)反应的机制具有重要的临床意义。在此我们表明,muOR与δ阿片受体(deltaOR)的异源二聚化导致β-抑制蛋白2组成性募集到受体复合物中,从而导致ERK1/2信号的时空调节发生变化。在细胞中内源性表达异源二聚体时使用β-抑制蛋白2的小干扰RNA(siRNA)进行的研究进一步支持了β-抑制蛋白2的参与。用muOR激动剂(DAMGO)和deltaOR拮抗剂(Tipp(psi))联合处理可改变β-抑制蛋白2与异源二聚体的结合,这导致ERK1/2磷酸化模式转变为单独使用muOR时观察到的模式。这些数据表明,在初始状态下,muOR-deltaOR异源二聚体处于有利于β-抑制蛋白介导信号传导的构象。用muOR和deltaOR配体联合处理使这种构象不稳定,导致转变为非β-抑制蛋白介导的信号传导。综上所述这些结果首次表明,muOR-deltaOR异源二聚体通过差异募集β-抑制蛋白,调节阿片受体信号传导的时空动态。