Mills Robyn E, Lam Viola C, Tan Allison, Cresalia Nicole, Oksenberg Nir, Zikherman Julie, Anderson Mark, Weiss Arthur, Hermiston Michelle L
Department of Pediatrics, University of California San Francisco, San Francisco, CA 94143; Biomedical Sciences Graduate Program, University of California San Francisco, San Francisco, CA 94143;
Department of Pediatrics, University of California San Francisco, San Francisco, CA 94143;
J Immunol. 2015 Apr 15;194(8):3675-86. doi: 10.4049/jimmunol.1500026. Epub 2015 Mar 13.
The autoimmune disease systemic lupus erythematosus has a complex environmental and multifactorial genetic basis. Genome-wide association studies have recently identified numerous disease-associated polymorphisms, but it remains unclear in which cells and during which step of pathogenesis specific polymorphisms interact to cause disease. Using a mouse model in which the same activating mutation (CD45E613R) causes distinct genetic background-dependent disease phenotypes, we performed a screen for genetic modifiers of autoreactivity between anti-nuclear Ab (ANA)-resistant CD45E613R.B6 and ANA-permissive CD45E613R.BALB/c mice. Within a novel autoreactivity-associated locus on chromosome 9, we identify a putative modifier, TLR9. Validating a role for TLR9 in modifying autoreactivity in the context of the CD45E613R mutation, manipulation of TLR9 gene dosage eliminates ANA in CD45E613R.BALB/c mice, but confoundingly permits ANA in CD45E613R.B6 mice. We demonstrate that sensitivity to ANA is modulated by strength of TLR9 signal, because stronger TLR9(B6) signals, but not weaker TLR9(BALB/c) signals, negatively regulate CD45E613R B cell development during competitive reconstitution at the central tolerance checkpoint. Our results identify a novel autoreactivity-associated locus and validate Tlr9 as a candidate gene within the locus. We further demonstrate a novel role for TLR9 signal strength in central tolerance, providing insight into the interplay of disease-associated polymorphisms at a discrete step of systemic lupus erythematosus pathogenesis.
自身免疫性疾病系统性红斑狼疮具有复杂的环境和多因素遗传基础。全基因组关联研究最近已鉴定出众多与疾病相关的多态性,但仍不清楚特定多态性在哪些细胞以及发病机制的哪个步骤相互作用而导致疾病。利用一种小鼠模型,其中相同的激活突变(CD45E613R)会导致不同的遗传背景依赖性疾病表型,我们针对抗核抗体(ANA)抗性的CD45E613R.B6和ANA允许性的CD45E613R.BALB/c小鼠之间的自身反应性遗传修饰因子进行了筛选。在9号染色体上一个新的与自身反应性相关的基因座内,我们鉴定出一个假定的修饰因子TLR9。在CD45E613R突变的背景下验证TLR9在修饰自身反应性中的作用时,对TLR9基因剂量的操作消除了CD45E613R.BALB/c小鼠中的ANA,但令人困惑的是,却使CD45E613R.B6小鼠中出现了ANA。我们证明对ANA的敏感性受TLR9信号强度的调节,因为更强的TLR9(B6)信号而非较弱的TLR9(BALB/c)信号在中枢耐受检查点的竞争性重建过程中对CD45E613R B细胞发育起负调节作用。我们的结果鉴定出一个新的与自身反应性相关的基因座,并验证Tlr9为该基因座内的一个候选基因。我们进一步证明了TLR9信号强度在中枢耐受中的新作用,为系统性红斑狼疮发病机制的一个离散步骤中疾病相关多态性的相互作用提供了见解。