Suzuki H, Takei M, Nakahata T, Fukamachi H
Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Gunma, Japan.
Biochem Biophys Res Commun. 1998 Jan 26;242(3):697-702. doi: 10.1006/bbrc.1997.8040.
Adenosine is a potent bronchoconstricting agent that is released by activated mast cells and hypoxic lung tissue. However, both inhibition and stimulation of mediator release from human lung mast cells by adenosine have been described, and this discrepancy seems to be due to contaminating cells or the effects of enzymatic treatment. We, therefore, investigated the effects of adenosine and its receptor-specific analogues on human cultured mast cells (HCMC). Adenosine inhibited Fc epsilon RI-mediated tryptase release from HCMC in a dose-dependent manner, and this inhibitory effect was completely blocked by the A2a receptor antagonist ZM241385. The specific agonist of A2a adenosine receptors CGS21680 inhibited the release of tryptase more potently than A1 and A3 agonists, and A2a receptor mRNA was detected by RT-PCR, suggesting the involvement of A2a receptors in the inhibitory effects of adenosine. In addition, adenosine increased intracellular cAMP level in a dose-dependent manner and inhibited protein tyrosine phosphorylation including that of ERK-2. These results suggest that adenosine acts via A2 receptors to inhibit Fc epsilon RI-mediated mediator release from human mast cells.
腺苷是一种由活化的肥大细胞和缺氧肺组织释放的强效支气管收缩剂。然而,腺苷对人肺肥大细胞介质释放的抑制和刺激作用均有报道,这种差异似乎是由于污染细胞或酶处理的影响所致。因此,我们研究了腺苷及其受体特异性类似物对人培养肥大细胞(HCMC)的影响。腺苷以剂量依赖性方式抑制HCMC中FcεRI介导的类胰蛋白酶释放,且这种抑制作用被A2a受体拮抗剂ZM241385完全阻断。A2a腺苷受体的特异性激动剂CGS21680比A1和A3激动剂更有效地抑制类胰蛋白酶的释放,并且通过RT-PCR检测到A2a受体mRNA,提示A2a受体参与了腺苷的抑制作用。此外,腺苷以剂量依赖性方式增加细胞内cAMP水平,并抑制包括ERK-2在内的蛋白质酪氨酸磷酸化。这些结果表明,腺苷通过A2受体发挥作用,抑制人肥大细胞中FcεRI介导的介质释放。