Lymphocyte Interaction Laboratory, Cancer Research UK London Research Institute, Lincoln's Inn Fields Laboratories, London WC2A 3LY, United Kingdom.
Cold Spring Harb Perspect Biol. 2011 Feb 1;3(2):a002360. doi: 10.1101/cshperspect.a002360.
B cells contribute to protective adaptive immune responses through generation of antibodies and long-lived memory cells, following engagement of the B-cell receptor (BCR) with specific antigen. Recent imaging investigations have offered novel insights into the ensuing molecular and cellular events underlying B-cell activation. Following engagement with antigen, BCR microclusters form and act as sites of active signaling through the recruitment of intracellular signaling molecules and adaptors. Signaling through these "microsignalosomes" is propagated and enhanced through B-cell spreading in a CD19-dependent manner. Subsequently, the mature immunological synapse is formed, and functions as a platform for antigen internalization, enabling the antigen presentation to helper T cells required for maximal B-cell activation. In this review, we discuss the emerging and critical role for the cytoskeleton in the coordination and regulation of these molecular events during B-cell activation.
B 细胞通过生成抗体和长寿记忆细胞来贡献保护性适应性免疫应答,这是在 B 细胞受体(BCR)与特定抗原结合后发生的。最近的成像研究为 B 细胞活化所涉及的后续分子和细胞事件提供了新的见解。与抗原结合后,BCR 微簇形成,并通过募集细胞内信号分子和衔接蛋白作为活性信号的位点发挥作用。这些“微信号体”的信号通过 B 细胞以依赖 CD19 的方式扩散来进行传递和增强。随后,成熟的免疫突触形成,并作为抗原内化的平台,使抗原能够呈递给辅助 T 细胞,这是 B 细胞最大活化所必需的。在这篇综述中,我们讨论了细胞骨架在 B 细胞活化过程中协调和调节这些分子事件中的新兴和关键作用。