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Expression of non-secreted IL-4 is associated with HDAC inhibitor-induced cell death histone acetylation and c-Jun regulation in human gamma/delta T-cells

机译:非分泌IL-4的表达与人类γ/δT细胞中HDAC抑制剂诱导的细胞死亡组蛋白乙酰化和c-Jun调节有关

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摘要

Previously, the expression of a non-secreted IL-4 variant (IL-4δ13) has been described in association with apoptosis and age-dependent Th2 T-cell polarization. Signaling pathways involved in this process have so far not been studied. Here we report the induction of IL-4δ13 expression in human γδ T-cells upon treatment with a sublethal dose of histone deacetylase (HDACi) inhibitor valproic acid (VPA). Induction of IL-4δ13 was associated with increased cytoplasmic IL-4Rα and decreased IL-4 expression, while mRNA for mature IL-4 was concomitantly down-regulated. Importantly, only the simultaneous combination of apoptosis and necroptosis inhibitors prevented IL-4δ13 expression and completely abrogated VPA-induced global histone H3K9 acetylation mark. Further, our work reveals a novel involvement of transcription factor c-Jun in the signaling network of IL-4, HDAC1, caspase-3 and mixed lineage kinase domain-like protein (MLKL). This study provides novel insights into the effects of epigenetic modulator VPA on human γδ T-cell differentiation.
机译:以前,已经描述了非分泌性IL-4变体(IL-4δ13)的表达与细胞凋亡和年龄依赖性Th2 T细胞极化有关。迄今为止,尚未研究此过程中涉及的信号传导途径。在这里,我们报道了用亚致死剂量的组蛋白脱乙酰基酶(HDACi)抑制剂丙戊酸(VPA)治疗后,人γδT细胞中IL-4δ13表达的诱导。 IL-4δ13的诱导与细胞质IL-4Rα的增加和IL-4表达的降低有关,而成熟IL-4的mRNA则随之下调。重要的是,只有细胞凋亡和坏死病抑制剂的同时使用才能阻止IL-4δ13表达,并完全消除VPA诱导的整体组蛋白H3K9乙酰化标记。此外,我们的工作揭示了转录因子c-Jun在IL-4,HDAC1,caspase-3和混合谱系激酶结构域样蛋白(MLKL)的信号网络中的新参与。该研究为表观遗传调节剂VPA对人γδT细胞分化的影响提供了新颖的见解。

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