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Iron-dependent histone 3 lysine 9 demethylation controls B cell proliferation and humoral immune responses

机译:铁依赖性组蛋白3赖氨酸9脱甲基控制B细胞增殖和体液免疫反应

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摘要

Trace elements play important roles in human health, but little is known about their functions in humoral immunity. Here, we show an important role for iron in inducing cyclin E and B cell proliferation. We find that iron-deficient individuals exhibit a significantly reduced antibody response to the measles vaccine when compared to iron-normal controls. Mice with iron deficiency also exhibit attenuated T-dependent or T-independent antigen-specific antibody responses. We show that iron is essential for B cell proliferation; both iron deficiency and α-ketoglutarate inhibition could suppress cyclin E1 induction and S phase entry of B cells upon activation. Finally, we demonstrate that three demethylases, KDM2B, KDM3B and KDM4C, are responsible for histone 3 lysine 9 (H3K9) demethylation at the cyclin E1 promoter, cyclin E1 induction and B cell proliferation. Thus, our data reveal a crucial role of H3K9 demethylation in B cell proliferation, and the importance of iron in humoral immunity.
机译:微量元素在人类健康中起着重要的作用,但是人们对它们在体液免疫中的功能知之甚少。在这里,我们显示了铁在诱导细胞周期蛋白E和B细胞增殖中的重要作用。我们发现,与铁正常对照相比,铁缺乏的个体对麻疹疫苗的抗体反应显着降低。铁缺乏症的小鼠也表现出减弱的T依赖性或T依赖性抗原特异性抗体反应。我们证明铁对于B细胞的增殖至关重要。铁缺乏和α-酮戊二酸的抑制均可以抑制细胞周期蛋白E1的诱导和激活后B细胞的S期进入。最后,我们证明了三个脱甲基酶KDM2B,KDM3B和KDM4C负责在细胞周期蛋白E1启动子,细胞周期蛋白E1诱导和B细胞增殖中的组蛋白3赖氨酸9(H3K9)去甲基化。因此,我们的数据揭示了H3K9去甲基化在B细胞增殖中的关键作用,以及铁在体液免疫中的重要性。

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