Department of Immune Regulation, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Bunkyo-ku, Tokyo, Japan.
Int Immunol. 2018 Aug 30;30(9):391-396. doi: 10.1093/intimm/dxy026.
Basophils and mast cells share some features, including basophilic granules in the cytoplasm, cell surface expression of the high-affinity IgE receptor and release of chemical mediators such as histamine. Because of this similarity and their minority status, basophils had often been erroneously considered as minor relatives or blood-circulating precursors of tissue-resident mast cells, and therefore long been neglected or underestimated in immunological studies. Taking advantage of newly developed tools, such as basophil-depleting antibodies and engineered mice deficient for only basophils, recent studies have identified previously unappreciated roles for basophils, distinct from those played by mast cells, in allergic responses, protective immunity against parasitic infections and regulation of other immune cells. In this review, we focus on two topics that we presented and discussed in the 46th Annual Meeting of the Japanese Society for Immunology held in Sendai in December 2017. The first topic is the function of basophils as antigen-presenting cells for driving Th2 cell differentiation. We demonstrated that basophils produce few or no MHC class II (MHC-II) proteins by themselves although they can acquire peptide-MHC-II complexes from dendritic cells through trogocytosis, and present them and provide IL-4 to naive CD4 T cells, promoting Th2 cell differentiation. The second topic is the basophil-specific effector molecules involved in allergic responses. Among mouse mast cell proteases (mMCPs), mMCP-8 and mMCP-11 are expressed almost exclusively by basophils. Analyses in vitro and in vivo revealed that both proteases can induce leukocyte migration through distinct mechanisms, contributing to the development of basophil-dependent allergic inflammation.
嗜碱性粒细胞和肥大细胞具有一些共同特征,包括细胞质中的嗜碱性颗粒、高亲和力 IgE 受体的细胞表面表达和化学介质如组胺的释放。由于这种相似性和它们的少数状态,嗜碱性粒细胞常常被错误地认为是组织驻留肥大细胞的次要亲属或血液循环前体,因此在免疫学研究中长期被忽视或低估。利用新开发的工具,如嗜碱性粒细胞耗竭抗体和仅缺乏嗜碱性粒细胞的工程小鼠,最近的研究已经确定了嗜碱性粒细胞在过敏反应、保护性免疫寄生虫感染和调节其他免疫细胞中以前未被认识到的作用,与肥大细胞不同。在这篇综述中,我们重点介绍了我们在 2017 年 12 月于仙台举行的第 46 届日本免疫学学会年会上展示和讨论的两个主题。第一个主题是嗜碱性粒细胞作为抗原呈递细胞驱动 Th2 细胞分化的功能。我们证明,尽管嗜碱性粒细胞可以通过胞饮作用从树突状细胞获取肽-MHC-II 复合物,但它们本身很少或不产生 MHC Ⅱ类(MHC-II)蛋白,并将其呈递给幼稚 CD4 T 细胞,并提供 IL-4,从而促进 Th2 细胞分化。第二个主题是参与过敏反应的嗜碱性粒细胞特异性效应分子。在鼠肥大细胞蛋白酶(mMCPs)中,mMCP-8 和 mMCP-11 几乎仅由嗜碱性粒细胞表达。体外和体内分析表明,这两种蛋白酶都可以通过不同的机制诱导白细胞迁移,有助于嗜碱性粒细胞依赖性过敏炎症的发展。