Institute of Immunology, University Hospital Ulm, 89081 Ulm, Germany.
Department of Molecular Immunology, Faculty of Biology, Albert-Ludwigs University of Freiburg, 79104 Freiburg, Germany; Max-Planck-Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany; Center for Biological Signaling Studies (BIOSS), Albert-Ludwigs University of Freiburg, 79104 Freiburg, Germany.
Trends Immunol. 2016 May;37(5):310-320. doi: 10.1016/j.it.2016.03.004. Epub 2016 Apr 1.
Expression of a functional B cell antigen receptor (BCR) plays a central role in regulating B cell development, maturation, and effector functions. Although IgM is solely expressed in immature B cell stages, the presence of both IgM- and IgD-BCR isotypes on mature naïve B cells raises the question of whether IgD has a unique role in B cell activation and function. While earlier studies suggested a broad functional redundancy between IgM and IgD, recent data point to an important immune regulatory role of IgD. Herein, we review these findings and discuss how the structural flexibility, mode of antigen binding, and co-receptor interactions, enable the IgD-BCR to act as a 'rheostat', regulating the activation and function of mature naïve B cells.
功能性 B 细胞抗原受体 (BCR) 的表达在调节 B 细胞的发育、成熟和效应功能方面起着核心作用。尽管 IgM 仅在未成熟 B 细胞阶段表达,但成熟的初始 B 细胞上同时存在 IgM 和 IgD-BCR 两种同种型,这就提出了 IgD 是否在 B 细胞激活和功能中具有独特作用的问题。虽然早期的研究表明 IgM 和 IgD 之间存在广泛的功能冗余,但最近的数据表明 IgD 具有重要的免疫调节作用。本文综述了这些发现,并讨论了 IgD-BCR 如何通过结构灵活性、抗原结合模式和共受体相互作用,充当“变阻器”,调节成熟初始 B 细胞的激活和功能。