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干扰素可诱导静息期CD4 T细胞中的APOBEC3G磷酸化

Interferon Induces The Phosphorylation of APOBEC3G In Resting CD4 T Cells

中文摘要英文摘要

目的:揭示干扰素对静息期CD4 T细胞中APOBEC3G (A3G) 磷酸化的诱导作用。方法:从人外周血中分离原代CD4 T细胞,构建pcDNA3.1-A3G-HA真核表达质粒并将其转染至静息期CD4 T细胞;将转染后的细胞分为对照组和IFN-α处理组,利用免疫共沉淀的方法检测在干扰素作用下的静息期CD4 T细胞中A3G蛋白的磷酸化情况。结果:在人类静息期CD4 T细胞中,IFN-α可诱导A3G 发生显著的磷酸化。结论:干扰素可诱导静息期CD4 T细胞中的A3G发生磷酸化,预示着IFN-α可通过某些信号通路对A3G进行翻译后修饰,其分子机理有待于深入研究。

OBJECTIVE: To reveal the phosphorylation effect of interferon on APOBEC3G (A3G) in resting CD4 T cells. METHODS: A3G gene with HA-tag was amplified and cloned into eukaryotic expression vector pcDNA3.1 to construct plasmid pcDNA3.1-A3G-HA, and then, isolated CD4 T cells from human peripheral blood. The recombinant plasmid was transfected into resting CD4 T cells by nucleofector and the transfected cells were equally divided into two groups (control group and experimental groups). Then, the experimental group was treated by IFN-α. The phosphorylation of A3G in resting CD4 T cells was detected after co-immunoprecipitation (co-IP). RESULTS: Interferon can induce significant phosphorylation of A3g in resting CD4 T cells. CONCLUSIONS: Interferon induces the phosphorylation of A3G in resting CD4 T cells. This phenomenoncan indicates that IFN-α may be responsible for post-translation modification of A3G through some signal pathways and its molecular mechanism remains to be clarified.

罗海华、刘超、张辉、张旭、陈灿灿、尹悦

基础医学分子生物学生物化学

干扰素POBEC3GHIV-1磷酸化

InterferonAPOBEC3GHIV-1Phosphorylation

罗海华,刘超,张辉,张旭,陈灿灿,尹悦.干扰素可诱导静息期CD4 T细胞中的APOBEC3G磷酸化[EB/OL].(2013-04-02)[2025-08-16].http://www.paper.edu.cn/releasepaper/content/201304-94.点此复制

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