Department of Pharmacotherapy, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, Japan.
PharmaCenter Bonn, Pharmaceutical Institute, Pharmaceutical Chemistry I, University of Bonn, An der Immenburg 4, D-53121 Bonn, Germany.
Immun Inflamm Dis. 2018 Mar;6(1):97-105. doi: 10.1002/iid3.200. Epub 2017 Nov 1.
Mast cells play an important role in allergic responses.
We herein demonstrated the mechanisms of inhibitory effect of adenine on IgE/antigen-induced degranulation and TNF-α release in mast cells.
We found that these effects were dependent on the amino group of adenine because purine only weakly inhibited degranulation. Adenine also inhibited Ca ionophore- and thapsigargin-induced degranulation, however, this inhibitory effect was weaker than that of the antigen. Therefore, the inhibitory effects of adenine on degranulation may be mediated before as well as after the Ca raise under the antigen stimulus. Adenine inhibited antigen-induced Syk and the subsequent induction of AKT and ERK activation under FcϵRI-mediated signal. Adenine also attenuated antigen-induced increase in Ca . Furthermore, adenine inhibited IgE/antigen-induced IKKα/β activation, which is involved in degranulation. Finally, adenine protected mice against anaphylactic allergic responses in vivo.
The present study revealed a key role of adenine in the attenuation of allergic responses through the inhibition of Syk-mediated signal transduction and IKK-mediated degranulation.
肥大细胞在过敏反应中发挥重要作用。
本研究旨在探讨腺嘌呤抑制 IgE/抗原诱导的肥大细胞脱颗粒和 TNF-α释放的作用机制。
我们发现这些作用依赖于腺嘌呤的氨基,因为嘌呤对脱颗粒的抑制作用较弱。腺嘌呤还抑制离子载体和毒胡萝卜素诱导的脱颗粒,但这种抑制作用弱于抗原。因此,腺嘌呤对脱颗粒的抑制作用可能在抗原刺激下钙升高之前和之后通过介导。腺嘌呤抑制抗原诱导的 Syk 及其随后诱导的 AKT 和 ERK 激活,这是 FcεRI 介导的信号转导的下游事件。腺嘌呤还减弱了抗原诱导的 Ca 增加。此外,腺嘌呤抑制 IgE/抗原诱导的 IKKα/β激活,这涉及脱颗粒。最后,腺嘌呤在体内保护小鼠免受过敏性过敏反应。
本研究揭示了腺嘌呤通过抑制 Syk 介导的信号转导和 IKK 介导的脱颗粒在减轻过敏反应中的关键作用。