Hikida Masaki, Casola Stefano, Takahashi Noriko, Kaji Tomohiro, Takemori Toshitada, Rajewsky Klaus, Kurosaki Tomohiro
Laboratory for Lymphocyte Differentiation, Research Center for Allergy and Immunology, RIKEN, Yokohama, Kanagawa 230-0045, Japan.
J Exp Med. 2009 Mar 16;206(3):681-9. doi: 10.1084/jem.20082100. Epub 2009 Mar 9.
Resting antigen-experienced memory B cells are thought to be responsible for the more rapid and robust antibody responses after antigen reencounter, which are the hallmark of memory humoral responses. The molecular basis for the development and survival of memory B cells remains largely unknown. We report that phospholipase C (PLC) gamma2 is required for efficient formation of germinal center (GC) and memory B cells. Moreover, memory B cell homeostasis is severely hampered by inducible loss of PLC-gamma2. Accordingly, mice with a conditional deletion of PLC-gamma2 in post-GC B cells had an almost complete abrogation of the secondary antibody response. Collectively, our data suggest that PLC-gamma2 conveys a survival signal to GC and memory B cells and that this signal is required for a productive secondary immune response.
静息的抗原接触过的记忆B细胞被认为是抗原再次接触后更快速、更强烈的抗体反应的原因,而这种反应是记忆性体液反应的标志。记忆B细胞发育和存活的分子基础在很大程度上仍然未知。我们报告,磷脂酶C(PLC)γ2是生发中心(GC)和记忆B细胞高效形成所必需的。此外,PLC-γ2的诱导性缺失严重阻碍了记忆B细胞的稳态。因此,GC后B细胞中PLC-γ2条件性缺失的小鼠几乎完全废除了二次抗体反应。总体而言,我们的数据表明,PLC-γ2向GC和记忆B细胞传递存活信号,并且该信号是有效的二次免疫反应所必需的。