Baba Yoshihiro, Matsumoto Masanori, Kurosaki Tomohiro
Laboratory for Lymphocyte Differentiation, WPI Immunology Frontier Research Center (IFReC), Osaka University, Suita, Osaka 565-0871, Japan Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa 230-0045, Japan
Laboratory for Lymphocyte Differentiation, WPI Immunology Frontier Research Center (IFReC), Osaka University, Suita, Osaka 565-0871, Japan Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Kanagawa 230-0045, Japan.
Int Immunol. 2015 Oct;27(10):487-93. doi: 10.1093/intimm/dxv027. Epub 2015 May 8.
The fundamental concepts surrounding B cells with inhibitory function (regulatory B cells) are now being established. In the context of autoimmune and inflammatory animal models, B cells play an immunomodulatory role via IL-10 production and contribute to limitation of the pathogenesis. Recent studies have notably identified the human counterparts of these cells, which have been suggested to be relevant to the pathophysiology of disease. Clear criteria to identify these cell subsets and the key molecular mechanisms underlying their physiological features are required for understanding the big picture of regulatory B cells. Plasmablasts have recently been identified as a major IL-10-producing regulatory B-cell subset and Ca(2+) signaling has furthermore been found to contribute to B-cell IL-10 expression. In this review, the signaling components controlling IL-10-dependent B-cell regulatory function and the development of IL-10-competent/-producing B cells and plasmablasts are discussed.
围绕具有抑制功能的B细胞(调节性B细胞)的基本概念正在逐步确立。在自身免疫和炎症动物模型的背景下,B细胞通过产生白细胞介素-10发挥免疫调节作用,并有助于限制发病机制。最近的研究特别鉴定出了这些细胞在人类中的对应物,有人认为它们与疾病的病理生理学相关。要全面了解调节性B细胞,需要明确识别这些细胞亚群的标准以及其生理特征背后的关键分子机制。浆母细胞最近被确定为主要产生白细胞介素-10的调节性B细胞亚群,此外还发现钙信号有助于B细胞白细胞介素-10的表达。在这篇综述中,我们讨论了控制白细胞介素-10依赖性B细胞调节功能的信号成分以及具有产生白细胞介素-10能力的B细胞和浆母细胞的发育。