Gunji Yoshitaka, Matsumura Takayoshi, Karasawa Tadayoshi, Komada Takanori, Baatarjav Chintogtokh, Komori Satoko, Aizawa Hidetoshi, Mizushina Yoshiko, Tsuda Hidetoshi, Miyake Kensuke, Maruyama Takashi, Ohmori Tsukasa, Karasuyama Hajime, Takahashi Masafumi
Division of Inflammation Research, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.
Division of Cardiovascular and Genetic Research, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan.
Cell Death Discov. 2025 Jul 27;11(1):346. doi: 10.1038/s41420-025-02630-6.
Atopic dermatitis (AD) is a chronic inflammatory skin disorder caused by immune dysregulation that involves the release of various pro-inflammatory cytokines. Patients with AD frequently exhibit basophil infiltration in the affected skin. Although the role of the NLRP3 inflammasome in innate immune cells has been extensively studied, the contribution of the basophil inflammasome to the pathophysiology of AD remains to be elucidated. In this study, we demonstrated that IL-33 primes the NLRP3 inflammasome in basophils, leading to the production and release of mature IL-1β. Mechanistically, we showed that IL-33 stimulation induced pro-IL-1β and NLRP3 expression via the NF-κB and p38 MAPK pathways and that basophils released mature IL-1β through the canonical inflammasome activation pathway, which requires NLRP3, ASC, caspase-1, and gasdermin D (GSDMD). In an oxazolone (OXA)-induced AD mouse model, we found that basophils acted as key initiators of inflammation by producing IL-1β in the lesion, and that basophil depletion, genetic ablation of Nlrp3 or Il1b, or basophil-specific genetic ablation of Nlrp3 ameliorated ear swelling and neutrophil infiltration. Collectively, these findings establish basophils as a significant early source of NLRP3 inflammasome-driven IL-1β, contributing to the pathogenesis of AD. Targeting the IL-33/ST2L axis or NLRP3 inflammasome activation in basophils may offer a promising therapeutic strategy for managing AD.
特应性皮炎(AD)是一种由免疫失调引起的慢性炎症性皮肤病,涉及多种促炎细胞因子的释放。AD患者在受累皮肤中常表现出嗜碱性粒细胞浸润。尽管NLRP3炎性小体在先天免疫细胞中的作用已得到广泛研究,但嗜碱性粒细胞炎性小体对AD病理生理学的贡献仍有待阐明。在本研究中,我们证明IL-33可启动嗜碱性粒细胞中的NLRP3炎性小体,导致成熟IL-1β的产生和释放。从机制上讲,我们表明IL-33刺激通过NF-κB和p38 MAPK途径诱导前体IL-1β和NLRP3表达,并且嗜碱性粒细胞通过经典的炎性小体激活途径释放成熟IL-1β,该途径需要NLRP3、ASC、半胱天冬酶-1和gasdermin D(GSDMD)。在恶唑酮(OXA)诱导的AD小鼠模型中,我们发现嗜碱性粒细胞通过在病变中产生IL-1β而成为炎症的关键启动者,并且嗜碱性粒细胞耗竭、Nlrp3或Il1b的基因敲除,或嗜碱性粒细胞特异性Nlrp3基因敲除可改善耳部肿胀和中性粒细胞浸润。总的来说,这些发现确立了嗜碱性粒细胞是NLRP3炎性小体驱动的IL-1β的重要早期来源,对AD的发病机制有贡献。靶向嗜碱性粒细胞中的IL-33/ST2L轴或NLRP3炎性小体激活可能为AD的治疗提供一种有前景的策略。