Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224-6825, USA.
J Pharmacol Exp Ther. 2012 Oct;343(1):157-66. doi: 10.1124/jpet.112.195206. Epub 2012 Jul 9.
Inhibition of cell proliferation by fenoterol and fenoterol derivatives in 1321N1 astrocytoma cells is consistent with β(2)-adrenergic receptor (β(2)-AR) stimulation. However, the events that result in fenoterol-mediated control of cell proliferation in other cell types are not clear. Here, we compare the effect of the β(2)-AR agonists (R,R')-fenoterol (Fen) and (R,R')-4-methoxy-1-naphthylfenoterol (MNF) on signaling and cell proliferation in HepG2 hepatocarcinoma cells by using Western blotting and [(3)H]thymidine incorporation assays. Despite the expression of β(2)-AR, no cAMP accumulation was observed when cells were stimulated with isoproterenol or Fen, although the treatment elicited both mitogen-activated protein kinase and phosphatidylinositol 3-kinase/Akt activation. Unexpectedly, isoproterenol and Fen promoted HepG2 cell growth, but MNF reduced proliferation together with increased apoptosis. The mitogenic responses of Fen were attenuated by 3-(isopropylamino)-1-[(7-methyl-4-indanyl)oxy]butan-2-ol (ICI 118,551), a β(2)-AR antagonist, whereas those of MNF were unaffected. Because of the coexpression of β(2)-AR and cannabinoid receptors (CBRs) and their impact on HepG2 cell proliferation, these Gα(i)/Gα(o)-linked receptors may be implicated in MNF signaling. Cell treatment with (R)-(+)-[2,3-dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl]-1-napthalenylmethanone (WIN 55,212-2), a synthetic agonist of CB(1)R and CB(2)R, led to growth inhibition, whereas inverse agonists of these receptors blocked MNF mitogenic responses without affecting Fen signaling. MNF responses were sensitive to pertussis toxin. The β(2)-AR-deficient U87MG cells were refractory to Fen, but responsive to the antiproliferative actions of MNF and WIN 55,212-2. The data indicate that the presence of the naphthyl moiety in MNF results in functional coupling to the CBR pathway, providing one of the first examples of a dually acting β(2)-AR-CBR ligand.
芬特罗及其衍生物对 1321N1 星形细胞瘤的细胞增殖抑制作用与β(2)-肾上腺素能受体(β(2)-AR)的刺激一致。然而,其他细胞类型中芬特罗介导的细胞增殖控制的结果尚不清楚。在这里,我们通过 Western blot 和 [(3)H]胸苷掺入实验比较了β(2)-AR 激动剂(R,R')-芬特罗(Fen)和(R,R')-4-甲氧基-1-萘基芬特罗(MNF)对 HepG2 肝癌细胞信号转导和细胞增殖的影响。尽管细胞表达β(2)-AR,但当用异丙肾上腺素或芬特罗刺激时,没有观察到 cAMP 积累,尽管该处理引发了丝裂原激活蛋白激酶和磷酸肌醇 3-激酶/ Akt 的激活。出乎意料的是,异丙肾上腺素和 Fen 促进了 HepG2 细胞的生长,但 MNF 降低了增殖,同时增加了细胞凋亡。ICI 118,551(一种β(2)-AR 拮抗剂)减弱了 Fen 的有丝分裂反应,而 MNF 的反应不受影响。由于β(2)-AR 和大麻素受体(CBRs)的共表达及其对 HepG2 细胞增殖的影响,这些 Gα(i)/Gα(o)-连接的受体可能与 MNF 信号转导有关。用(R)-(+)-[2,3-二氢-5-甲基-3-(4-吗啉基甲基)吡咯并[1,2,3-de]-1,4-苯并恶嗪-6-基]-1-萘基甲酮(WIN 55,212-2)处理细胞,一种 CB(1)R 和 CB(2)R 的合成激动剂,导致生长抑制,而这些受体的反向激动剂阻断了 MNF 的有丝分裂反应,而不影响 Fen 的信号转导。MNF 反应对百日咳毒素敏感。β(2)-AR 缺陷的 U87MG 细胞对 Fen 无反应,但对 MNF 和 WIN 55,212-2 的抗增殖作用有反应。数据表明,MNF 中萘基部分的存在导致与 CBR 途径的功能偶联,提供了第一个双重作用的β(2)-AR-CBR 配体之一。