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脱嘌呤/脱嘧啶核酸内切酶 1/氧化还原因子-1(Ape1/Ref-1)对于 IL-21 诱导的通过 ERK1/2 途径的信号转导是必需的。

Apurinic/apyrimidinic endonuclease1/redox factor-1 (Ape1/Ref-1) is essential for IL-21-induced signal transduction through ERK1/2 pathway.

机构信息

Department of Immunology, Yamagata University Faculty of Medicine, Yamagata, Japan.

出版信息

Biochem Biophys Res Commun. 2012 Apr 13;420(3):628-34. doi: 10.1016/j.bbrc.2012.03.051. Epub 2012 Mar 17.

Abstract

IL-21 is a pleiotropic cytokine that regulates T-cell and B-cell differentiation, NK-cell activation, and dendritic cell functions. IL-21 activates the JAK-STAT, ERK, and PI3K pathways. We report here that Ape1/Ref-1 has an essential role in IL-21-induced cell growth signal transduction. Overexpression of Ape1/Ref-1 enhances IL-21-induced cell proliferation, but it is suppressed by overexpressing an N-terminal deletion mutant of Ape1/Ref-1 that lacks the redox domain. Furthermore, knockdown of the Ape1/Ref-1 mRNA dramatically compromises IL-21-induced ERK1/2 activation and cell proliferation with increasing cell death. These impaired activities are recovered by the re-expression of Ape1/Ref-1 in the knockdown cells. Our findings are the first demonstration that Ape1/Ref-1 is an indispensable molecule for the IL-21-mediated signal transduction through ERK1/2 activation.

摘要

白细胞介素 21(IL-21)是一种多效细胞因子,可调节 T 细胞和 B 细胞分化、NK 细胞激活和树突状细胞功能。IL-21 激活 JAK-STAT、ERK 和 PI3K 通路。我们在此报告,Ape1/Ref-1 在 IL-21 诱导的细胞生长信号转导中具有重要作用。Ape1/Ref-1 的过表达增强了 IL-21 诱导的细胞增殖,但被表达缺乏氧化还原结构域的 N 端缺失突变体的 Ape1/Ref-1 抑制。此外,Ape1/Ref-1 mRNA 的敲低显著损害了 IL-21 诱导的 ERK1/2 激活和细胞增殖,同时增加细胞死亡。在敲低细胞中重新表达 Ape1/Ref-1 可恢复这些受损的活性。我们的研究结果首次表明,Ape1/Ref-1 是通过 ERK1/2 激活介导的 IL-21 信号转导所必需的分子。

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