Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada; email:
Life Sciences Institute, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.
Annu Rev Immunol. 2019 Apr 26;37:97-123. doi: 10.1146/annurev-immunol-042718-041704.
The B cell antigen receptor (BCR) plays a central role in the self/nonself selection of B lymphocytes and in their activation by cognate antigen during the clonal selection process. It was long thought that most cell surface receptors, including the BCR, were freely diffusing and randomly distributed. Since the advent of superresolution techniques, it has become clear that the plasma membrane is compartmentalized and highly organized at the nanometer scale. Hence, a complete understanding of the precise conformation and activation mechanism of the BCR must take into account the organization of the B cell plasma membrane. We review here the recent literature on the nanoscale organization of the lymphocyte membrane and discuss how this new information influences our view of the conformational changes that the BCR undergoes during activation.
B 细胞抗原受体 (BCR) 在 B 淋巴细胞的自身/非自身选择以及在克隆选择过程中通过同源抗原的激活中起着核心作用。长期以来,人们一直认为包括 BCR 在内的大多数细胞表面受体都是自由扩散和随机分布的。自从超分辨率技术问世以来,很明显,质膜在纳米尺度上是分隔的和高度组织化的。因此,要完全了解 BCR 的精确构象和激活机制,就必须考虑 B 细胞质膜的组织。在这里,我们回顾了关于淋巴细胞膜纳米尺度组织的最新文献,并讨论了这些新信息如何影响我们对 BCR 在激活过程中经历的构象变化的看法。