Lin Kai-Chun, Huang Duen-Yi, Huang De-Wei, Tzeng Shiang-Jong, Lin Wan-Wan
Department of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan.
J Mol Med (Berl). 2016 Feb;94(2):183-94. doi: 10.1007/s00109-015-1339-2. Epub 2015 Sep 16.
AMPK was shown to negatively regulate FcεRI activation, and FcεR-mediated Fyn activation can counteract the LKB1/AMPK axis in mast cells. However, the relationship between the major Src family kinase Lyn and AMPK remains poorly defined. Here, we investigate the molecular mechanism for AMPK inhibition by FcεRI-Lyn signaling in rat RBL-2H3 cells. We found that FcεRI activation could rapidly inhibit AMPK activation through increased AMPK phosphorylation at the inhibitory Ser485/491 residues without a change at the activating Th172 residue, and this was accompanied by a reduction of ACC phosphorylation. Using specific inhibitors and gene silencing, we found that such AMPK inhibition involved a signaling cascade through Lyn-Syk-Akt. When AMPK was activated by AICAR, A769662 and metformin, FcεRI-mediated Syk, ERK, JNK and p38 activation, and TNFα release were all inhibited. Consistently, AMPK inhibition by compound C increased FcεRI-mediated Lyn activation. Moreover, AMPK activation dominantly impaired IgE-induced recruitment of signal proteins to the FcεRI by blocking the formation of FcεRIβ-Lyn-Syk, FcεRIγ-Lyn-Syk, and AMPK-FcεRIβ complexes. In vitro kinase assay further revealed the ability of AMPKα2 to phosphorylate FcεRIβ in the complex. In vivo, AMPK activation by metformin could readily reduce vascular permeability and ear swelling in a mouse model of passive cutaneous anaphylaxis mediated by IgE. In summary, our findings demonstrate that IgE-mediated FcεRI activation results in AMPK inhibition through activation of Lyn-Syk-Akt pathway, and as such FcεRI receptor can efficiently propagate Lyn-mediated allergic signaling and response. These results provide important insights into the use of AMPK activators for the treatment of allergic diseases.
AMPK is inhibited by FcεRI via Lyn-Syk-Akt signaling in RBL-2H3 cells. AMPK inhibition supports FcεRI-mediated Lyn signaling and allergic response. Metformin has inhibitory effect on passive cutaneous anaphylaxis.
已表明AMPK对FcεRI激活起负调控作用,且FcεR介导的Fyn激活可在肥大细胞中抵消LKB1/AMPK轴的作用。然而,主要的Src家族激酶Lyn与AMPK之间的关系仍不清楚。在此,我们研究大鼠RBL - 2H3细胞中FcεRI - Lyn信号传导抑制AMPK的分子机制。我们发现FcεRI激活可通过增加AMPK在抑制性Ser485/491残基处的磷酸化而迅速抑制AMPK激活,而在激活的Th172残基处无变化,同时伴有ACC磷酸化的减少。使用特异性抑制剂和基因沉默,我们发现这种AMPK抑制涉及通过Lyn - Syk - Akt的信号级联反应。当AMPK被AICAR、A769662和二甲双胍激活时,FcεRI介导的Syk、ERK、JNK和p38激活以及TNFα释放均受到抑制。同样,化合物C抑制AMPK会增加FcεRI介导的Lyn激活。此外,AMPK激活主要通过阻断FcεRIβ - Lyn - Syk、FcεRIγ - Lyn - Syk和AMPK - FcεRIβ复合物的形成,损害IgE诱导的信号蛋白向FcεRI的募集。体外激酶分析进一步揭示了AMPKα2在复合物中磷酸化FcεRIβ的能力。在体内,二甲双胍激活AMPK可在由IgE介导的被动皮肤过敏反应小鼠模型中轻易降低血管通透性和耳部肿胀。总之,我们的数据表明IgE介导的FcεRI激活通过激活Lyn - Syk - Akt途径导致AMPK抑制,因此FcεRI受体可有效传播Lyn介导的过敏信号和反应。这些结果为使用AMPK激活剂治疗过敏性疾病提供了重要见解。
在RBL - 2H3细胞中,AMPK被FcεRI通过Lyn - Syk - Akt信号传导抑制。AMPK抑制支持FcεRI介导的Lyn信号传导和过敏反应。二甲双胍对被动皮肤过敏反应有抑制作用。