Department of Pharmacology & Toxicology, Institute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, USA.
Department of Pharmacology & Toxicology, Institute for Integrative Toxicology, Michigan State University, East Lansing, MI, 48824, USA.
Food Chem Toxicol. 2020 Nov;145:111595. doi: 10.1016/j.fct.2020.111595. Epub 2020 Jul 20.
Nrf2 is a transcription factor that regulates cytoprotective cellular responses to oxidative and electrophilic stress. Nrf2 is potently activated by the synthetic food additive, tert-butylhydroquinone (tBHQ), which is widely used as a preservative in oils and processed foods. Previously published studies have established that tBHQ has numerous effects on T cell function. The purpose of this study was to determine the effect of tBHQ on B cell function and the role of Nrf2 in these effects. Specifically, we investigated T cell-independent B cell activation, differentiation, and IgM antibody production. Murine wild-type and Nrf2-null splenocytes were isolated, treated with tBHQ (0.25-2.5 μm), and activated by lipopolysaccharide (LPS), a T cell-independent B cell activator. Our findings indicate that tBHQ significantly enhanced IgM production in activated wild-type, but not Nrf2-null, B cells, suggesting this effect is Nrf2-dependent. In contrast, tBHQ significantly decreased the induction of CD69, CD25, CD22, and CD138 in both wild-type and Nrf2-null splenocytes. These findings indicate that the tBHQ-mediated increase in IgM is Nrf2-dependent, whereas the inhibition of CD69, CD25, CD22 and CD138 is Nrf2-independent. Overall, this study demonstrates that in addition to its effects on T cells, tBHQ also has potent effects on T cell-independent B cell function.
Nrf2 是一种转录因子,可调节细胞对氧化和亲电应激的保护反应。Nrf2 被合成食品添加剂叔丁基对苯二酚(tBHQ)强烈激活,tBHQ 广泛用作油和加工食品的防腐剂。先前的研究已经确定 tBHQ 对 T 细胞功能有多种影响。本研究旨在确定 tBHQ 对 B 细胞功能的影响以及 Nrf2 在这些影响中的作用。具体来说,我们研究了 T 细胞非依赖性 B 细胞激活、分化和 IgM 抗体产生。分离了野生型和 Nrf2 敲除型小鼠脾细胞,用 tBHQ(0.25-2.5 μm)处理,并通过脂多糖(LPS)激活,LPS 是一种 T 细胞非依赖性 B 细胞激活剂。我们的研究结果表明,tBHQ 显著增强了激活的野生型 B 细胞中 IgM 的产生,但在 Nrf2 敲除型 B 细胞中没有,这表明这种作用依赖于 Nrf2。相比之下,tBHQ 显著降低了野生型和 Nrf2 敲除型脾细胞中 CD69、CD25、CD22 和 CD138 的诱导。这些发现表明,tBHQ 介导的 IgM 增加依赖于 Nrf2,而 CD69、CD25、CD22 和 CD138 的抑制则不依赖于 Nrf2。总体而言,这项研究表明,除了对 T 细胞的影响外,tBHQ 还对 T 细胞非依赖性 B 细胞功能具有强大的影响。