Department of Immunology and 2 Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710.
J Exp Med. 2014 Jan 13;211(1):57-69. doi: 10.1084/jem.20130648. Epub 2013 Dec 16.
Balanced transmembrane signals maintain a competent peripheral B cell pool limited in self-reactive B cells that may produce pathogenic autoantibodies. To identify molecules regulating peripheral B cell survival and tolerance to self-antigens (Ags), a gene modifier screen was performed with B cells from CD22-deficient C57BL/6 (CD22(-/-[B6])) mice that undergo activation-induced cell death (AICD) and fail to up-regulate c-Myc expression after B cell Ag receptor ligation. Likewise, lysozyme auto-Ag-specific B cells in Ig(Tg) hen egg lysozyme (HEL) transgenic mice inhabit the spleen but undergo AICD after auto-Ag encounter. This gene modifier screen identified EndoU, a single-stranded RNA-binding protein of ancient origin, as a major regulator of B cell survival in both models. EndoU gene disruption prevents AICD and normalizes c-Myc expression. These findings reveal that EndoU is a critical regulator of an unexpected and novel RNA-dependent pathway controlling peripheral B cell survival and Ag responsiveness that may contribute to peripheral B cell tolerance.
平衡的跨膜信号维持着一个有能力的外周 B 细胞池,该池中的自身反应性 B 细胞受到限制,这些 B 细胞可能产生致病性自身抗体。为了鉴定调节外周 B 细胞存活和对自身抗原(Ags)耐受的分子,对来自 CD22 缺陷的 C57BL/6(CD22(-/-[B6])) 小鼠的 B 细胞进行了基因修饰筛选,这些小鼠经历激活诱导的细胞死亡(AICD),并且在 B 细胞抗原受体交联后不能上调 c-Myc 表达。同样,Ig(Tg)母鸡卵溶菌酶(HEL)转基因小鼠中的溶菌酶自身抗原特异性 B 细胞栖息在脾脏中,但在自身抗原遇到后会发生 AICD。该基因修饰筛选鉴定出 EndoU 是一种古老起源的单链 RNA 结合蛋白,是这两种模型中 B 细胞存活的主要调节剂。EndoU 基因缺失可防止 AICD 并使 c-Myc 表达正常化。这些发现表明,EndoU 是一个出乎意料的新型 RNA 依赖性途径的关键调节因子,该途径控制外周 B 细胞的存活和 Ag 反应性,可能有助于外周 B 细胞耐受。