Institute for Chemical Safety Sciences, The Hamner Institutes for Health Sciences, NC 27709, USA.
Toxicol Appl Pharmacol. 2013 Apr 1;268(1):17-26. doi: 10.1016/j.taap.2013.01.015. Epub 2013 Jan 26.
Many environmental contaminants can disrupt the adaptive immune response. Exposure to the ubiquitous aryl hydrocarbon receptor (AhR) ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and other agonists suppresses the antibody response. The underlying pathway mechanism by which TCDD alters B cell function is not well understood. The present study investigated the mechanism of AhR-mediated pathways and mode of suppression by which TCDD perturbs terminal differentiation of B cells to plasma cells and thereby impairs antibody production. An integrated approach combining computational pathway modeling and in vitro assays with primary mouse B cells activated by lipopolysaccharide was employed. We demonstrated that suppression of the IgM response by TCDD occurs in an all-or-none (binary) rather than graded mode: i.e., it reduces the number of IgM-secreting cells in a concentration-dependent manner without affecting the IgM content in individual plasma cells. The mathematical model of the gene regulatory circuit underpinning B cell differentiation revealed that two previously identified AhR-regulated pathways, inhibition of signaling protein AP-1 and activation of transcription factor Bach2, could account for the all-or-none mode of suppression. Both pathways disrupt the operation of a bistable-switch circuit that contains transcription factors Bcl6, Prdm1, Pax5, and Bach2 and regulates B cell fate. The model further predicted that by transcriptionally activating Bach2, TCDD might delay B cell differentiation and increase the likelihood of isotype switching, thereby altering the antibody repertoire. In conclusion, the present study revealed the mode and specific pathway mechanisms by which the environmental immunosuppressant TCDD suppresses B cell differentiation.
许多环境污染物可破坏适应性免疫应答。接触无处不在的芳香烃受体 (AhR) 配体 2,3,7,8-四氯二苯并对二恶英 (TCDD) 和其他激动剂会抑制抗体应答。TCDD 改变 B 细胞功能的潜在途径机制尚不清楚。本研究调查了 AhR 介导的途径机制,以及 TCDD 通过何种方式干扰 B 细胞向浆细胞的终末分化,从而损害抗体产生。采用了一种综合方法,结合计算途径建模和体外测定,以及用脂多糖激活的原代小鼠 B 细胞。我们证明 TCDD 对 IgM 应答的抑制呈全有或全无(二进制)而非分级模式:即,它以浓度依赖性方式减少 IgM 分泌细胞的数量,而不影响单个浆细胞中的 IgM 含量。支持 B 细胞分化的基因调控回路的数学模型表明,先前鉴定的两种 AhR 调节途径,即抑制信号蛋白 AP-1 和激活转录因子 Bach2,可以解释全有或全无的抑制模式。这两种途径都破坏了包含转录因子 Bcl6、Prdm1、Pax5 和 Bach2 并调节 B 细胞命运的双稳态开关电路的运行。该模型进一步预测,通过转录激活 Bach2,TCDD 可能会延迟 B 细胞分化并增加同种型转换的可能性,从而改变抗体库。总之,本研究揭示了环境免疫抑制剂 TCDD 抑制 B 细胞分化的模式和特定途径机制。