Goupil Eugénie, Wisehart Veronica, Khoury Etienne, Zimmerman Brandon, Jaffal Sahar, Hébert Terence E, Laporte Stéphane A
Polypeptide Hormone Laboratory, Division of Endocrinology, Department of Medicine, McGill University Health Centre Research Institute, McGill University, Montreal, QC, Canada H3A 2B2.
Mol Endocrinol. 2012 Jul;26(7):1189-202. doi: 10.1210/me.2011-1245. Epub 2012 May 25.
The G protein-coupled prostaglandin F2α (PGF2α) receptor [F prostanoid (FP) receptor] has been implicated in many physiological events including cardiovascular, respiratory, immune, reproductive, and endocrine responses. Binding of PGF2α to FP receptor elicits inositol production and protein kinase C-dependent MAPK activation through Gα(q) coupling. Here we report that AL-8810, previously characterized as an orthosteric antagonist of PGF2α-dependent, Gα(q)-mediated signaling, potently activates ERK1/2 in a protein kinase C-independent manner. Rather, AL-8810 promoted ERK1/2 activation via an epidermal growth factor receptor transactivation mechanism in both human embryonic kidney 293 cells and in the MG-63 osteoblast-like cells, which express endogenous FP receptors. Neither AL-8810- nor PGF2α-mediated stimulation of FP receptor promoted association with β-arrestins, suggesting that MAPK activation induced by these ligands is independent of β-arrestin's signaling scaffold functions. Interestingly, the spatiotemporal activation of ERK1/2 promoted by AL-8810 and PGF2α showed almost completely opposite responses in the nucleus and the cytosol. Finally, using [(3)H]thymidine incorporation, we noted differential regulation of PGF2α- and AL-8810-induced cell proliferation in MG-63 cells. This study reveals, for the first time, the signaling biased nature of FP receptor orthosteric ligands toward MAPK signaling. Our findings on the specific patterns of ERK1/2 activation promoted by FP receptor ligands may help dissect the distinct roles of MAPK in FP receptor-dependent physiological responses.
G蛋白偶联前列腺素F2α(PGF2α)受体[F前列腺素(FP)受体]参与了许多生理活动,包括心血管、呼吸、免疫、生殖和内分泌反应。PGF2α与FP受体结合通过Gα(q)偶联引发肌醇生成和蛋白激酶C依赖性的MAPK激活。在此我们报告,AL-8810先前被表征为PGF2α依赖性、Gα(q)介导信号传导的正构拮抗剂,却能以不依赖蛋白激酶C的方式有效激活ERK1/2。相反,在表达内源性FP受体的人胚肾293细胞和MG-63成骨样细胞中,AL-8810通过表皮生长因子受体转活化机制促进ERK1/2激活。AL-8810和PGF2α对FP受体的刺激均未促进与β-抑制蛋白的结合,这表明这些配体诱导的MAPK激活独立于β-抑制蛋白的信号支架功能。有趣的是,AL-8810和PGF2α促进的ERK1/2在细胞核和细胞质中的时空激活显示出几乎完全相反的反应。最后,使用[³H]胸腺嘧啶掺入法,我们注意到PGF2α和AL-8810诱导的MG-63细胞增殖存在差异调节。本研究首次揭示了FP受体正构配体对MAPK信号传导的信号偏向性本质。我们关于FP受体配体促进ERK1/2激活的特定模式的发现可能有助于剖析MAPK在FP受体依赖性生理反应中的不同作用。