Oka Saori, Wakui Junichi, Ikeda Shinobu, Yanagimoto Shin, Kishimoto Seishi, Gokoh Maiko, Nasui Miwako, Sugiura Takayuki
Faculty of Pharmaceutical Sciences, Teikyo University, Sagamihara, Kanagawa 199-0195, Japan.
J Immunol. 2006 Dec 15;177(12):8796-805. doi: 10.4049/jimmunol.177.12.8796.
The possible involvement of 2-arachidonoylglycerol (2-AG), an endogenous ligand for the cannabinoid receptors (CB1 and CB2), in contact dermatitis in mouse ear was investigated. We found that the level of 2-AG was markedly elevated in the ear following a challenge with oxazolone in sensitized mice. Of note, the swelling following the challenge was suppressed by either the administration of SR144528, a CB2 receptor antagonist, immediately after sensitization, or the administration of SR144528 upon the challenge. The effect of AM251, a CB1 receptor antagonist, was marginal in either case. It seems apparent, therefore, that the CB2 receptor and its endogenous ligand 2-AG are closely involved in both the sensitization phase and the elicitation phase of oxazolone-induced contact dermatitis. In line with this, we found that Langerhans cells (MHC class II(+)) contain a substantial amount of CB2 receptor mRNA, whereas keratinocytes (MHC class II(-)) do not. We also obtained evidence that the expression of mRNAs for proinflammatory cytokines following a challenge with oxazolone was markedly suppressed by treatment with SR144528. We next examined whether the CB2 receptor and 2-AG participate in chronic contact dermatitis accompanied by the infiltration of tissues by eosinophils. The amount of 2-AG in mouse ear dramatically increased following repeated challenge with oxazolone. Importantly, treatment with SR144528 attenuated both the recruitment of eosinophils and ear swelling in chronic contact dermatitis induced by repeated challenge with oxazolone. These results strongly suggest that the CB2 receptor and 2-AG play important stimulative roles in the sensitization, elicitation, and exacerbation of allergic inflammation.
研究了大麻素受体(CB1和CB2)的内源性配体2-花生四烯酸甘油酯(2-AG)在小鼠耳部接触性皮炎中的可能作用。我们发现,在致敏小鼠中用恶唑酮激发后,耳部2-AG水平显著升高。值得注意的是,在致敏后立即给予CB2受体拮抗剂SR144528,或在激发时给予SR144528,均可抑制激发后的肿胀。在这两种情况下,CB1受体拮抗剂AM251的作用都很微弱。因此,很明显,CB2受体及其内源性配体2-AG在恶唑酮诱导的接触性皮炎的致敏阶段和激发阶段都密切相关。与此一致的是,我们发现朗格汉斯细胞(MHC II类(+))含有大量CB2受体mRNA,而角质形成细胞(MHC II类(-))则没有。我们还获得证据表明,用SR144528处理可显著抑制恶唑酮激发后促炎细胞因子mRNA的表达。接下来,我们研究了CB2受体和2-AG是否参与伴有嗜酸性粒细胞浸润组织的慢性接触性皮炎。在用恶唑酮反复激发后,小鼠耳部2-AG的量显著增加。重要的是,用SR144528处理可减轻恶唑酮反复激发诱导的慢性接触性皮炎中嗜酸性粒细胞的募集和耳部肿胀。这些结果强烈表明,CB2受体和2-AG在过敏性炎症的致敏、激发和加重中起重要的刺激作用。