Department of Immunology, Monash University, Melbourne, VIC 3004, Australia; Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia.
Immunity. 2013 Sep 19;39(3):573-83. doi: 10.1016/j.immuni.2013.05.019. Epub 2013 Sep 5.
Activation-induced cell death (AICD) plays a critical role in immune homeostasis and tolerance. In T-cell-dependent humoral responses, AICD of B cells is initiated by Fas ligand (FasL) on T cells, stimulating the Fas receptor on B cells. In contrast, T-cell-independent B cell responses involve innate-type B lymphocytes, such as marginal zone (MZ) B cells, and little is known about the mechanisms that control AICD during innate B cell responses to Toll-like receptor (TLR) activation. Here, we show that MZ B cells undergo AICD in response to TLR4 activation in vivo. The transmembrane activator, calcium modulator, and cyclophilin ligand interactor (TACI) receptor and TLR4 cooperate to upregulate expression of both FasL and Fas on MZ B cells and also to repress inhibitors of Fas-induced apoptosis signaling. These findings demonstrate an unappreciated role for TACI and its ligands in the regulation of AICD during T-cell-independent B cell responses.
活化诱导的细胞死亡 (AICD) 在免疫稳态和耐受中起着关键作用。在 T 细胞依赖性体液反应中,T 细胞上的 Fas 配体 (FasL) 启动 B 细胞的 AICD,刺激 B 细胞上的 Fas 受体。相比之下,T 细胞非依赖性 B 细胞反应涉及先天型 B 淋巴细胞,如边缘区 (MZ) B 细胞,而对于控制先天 B 细胞对 Toll 样受体 (TLR) 激活的 AICD 的机制知之甚少。在这里,我们表明 MZ B 细胞在体内 TLR4 激活时发生 AICD。跨膜激活剂、钙调节剂和环孢素配体相互作用物 (TACI) 受体和 TLR4 合作上调 MZ B 细胞上 FasL 和 Fas 的表达,同时抑制 Fas 诱导的凋亡信号的抑制剂。这些发现表明 TACI 及其配体在 T 细胞非依赖性 B 细胞反应中调节 AICD 中的作用未被充分认识。