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淋巴细胞中广泛存在的含肌苷mRNA受ADAR1调节以响应炎症。

Widespread inosine-containing mRNA in lymphocytes regulated by ADAR1 in response to inflammation.

作者信息

Yang Jing-Hua, Luo Xiaoxing, Nie Yongzhan, Su Yingjun, Zhao Qingchuan, Kabir Koroush, Zhang Dexin, Rabinovici Reuven

机构信息

Department of Surgery, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Immunology. 2003 May;109(1):15-23. doi: 10.1046/j.1365-2567.2003.01598.x.

Abstract

Adenosine-to-inosine (A-to-I) RNA editing is a post-transcriptional modification of pre-mRNA catalysed by an RNA-specific adenosine deaminase (ADAR). A-to-I RNA editing has been previously reported in the pre-mRNAs of brain glutamate and serotonin receptors and in lung tissue during inflammation. Here we report that systemic inflammation markedly induces inosine-containing mRNA to approximately 5% of adenosine in total mRNA. Induction was the result of up-regulation of A-to-I RNA editing as both dsRNA editing activity and ADAR1 expression were increased in the spleen, thymus and peripheral lymphocytes from endotoxin-treated mice. Up-regulation of ADAR1 was confirmed in vitro in T lymphocytes and macrophages stimulated with a variety of inflammatory mediators including tumour necrosis factor-alpha and interferon-gamma. A late induction of RNA editing was detected in concanavalin A-activated splenocytes stimulated with interleukin-2 in vitro. Taken together, these data suggest that a large number of inosine-containing mRNAs are produced during acute inflammation via up-regulation of ADAR1-mediated RNA editing. These events may affect the inflammatory and immune response through modulation of protein production.

摘要

腺苷到次黄苷(A-to-I)RNA编辑是一种由RNA特异性腺苷脱氨酶(ADAR)催化的前体mRNA的转录后修饰。此前已报道在脑谷氨酸和5-羟色胺受体的前体mRNA以及炎症期间的肺组织中存在A-to-I RNA编辑。在此我们报道,全身炎症显著诱导含次黄苷的mRNA在总mRNA中占腺苷的比例达到约5%。这种诱导是A-to-I RNA编辑上调的结果,因为在内毒素处理小鼠的脾脏、胸腺和外周淋巴细胞中,双链RNA编辑活性和ADAR1表达均增加。在用包括肿瘤坏死因子-α和干扰素-γ在内的多种炎症介质刺激的T淋巴细胞和巨噬细胞中,体外证实了ADAR1的上调。在体外,用白细胞介素-2刺激伴刀豆球蛋白A激活的脾细胞时,检测到RNA编辑的晚期诱导。综上所述,这些数据表明在急性炎症期间,通过ADAR1介导的RNA编辑上调产生了大量含次黄苷的mRNA。这些事件可能通过调节蛋白质产生来影响炎症和免疫反应。

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