Davey Angel, Liu Wanli, Sohn Hae Won, Brzostowski Joseph, Pierce Susan K
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, NIH, Rockville, Maryland 20852.
Methods Enzymol. 2012;506:265-290. doi: 10.1016/B978-0-12-391856-7.00038-X.
Antibody responses are initiated by the binding of antigens to clonally distributed cell surface B cell receptors (BCRs) that trigger signaling cascades resulting in B cell activation. Using conventional biochemical approaches, the components of the downstream BCR signaling pathways have been described in considerable detail. However, far less is known about the early molecular events by which the binding of antigens to the BCRs initiates BCR signaling. With the recent advent of high resolution, high speed, live cell, and single molecule imaging technologies, these events are just beginning to be elucidated. Understanding the molecular mechanisms underlying the initiation of BCR signaling may provide new targets for therapeutics to block dysregulated BCR signaling in systemic autoimmune diseases and in B cell tumors and to aid in the design of protein subunit vaccines. In this chapter, we describe the general procedures for using these new imaging techniques to investigate the early events in the initiation of BCR signaling.
抗体反应是由抗原与克隆分布的细胞表面B细胞受体(BCR)结合引发的,BCR触发信号级联反应,导致B细胞活化。使用传统的生化方法,下游BCR信号通路的组成部分已得到相当详细的描述。然而,对于抗原与BCR结合引发BCR信号的早期分子事件,我们所知甚少。随着高分辨率、高速、活细胞和单分子成像技术的最新出现,这些事件才刚刚开始被阐明。了解BCR信号起始的分子机制可能为治疗提供新的靶点,以阻断系统性自身免疫性疾病和B细胞肿瘤中失调的BCR信号,并有助于设计蛋白质亚基疫苗。在本章中,我们描述了使用这些新成像技术研究BCR信号起始早期事件的一般程序。