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白细胞介素-4对小鼠巨噬细胞组成型β干扰素合成的抑制作用。

Inhibition by interleukin-4 of constitutive beta interferon synthesis in mouse macrophages.

作者信息

Nickolaus P, Zawatzky R

机构信息

Applied Tumor Virology Program, German Cancer Research Center, Heidelberg.

出版信息

J Virol. 1994 Oct;68(10):6763-6. doi: 10.1128/JVI.68.10.6763-6766.1994.

Abstract

We have found that interleukin-4 (IL-4) abrogated constitutive beta interferon (IFN-beta) synthesis in mouse macrophages. Analysis of endogenous IFN mRNA by reverse transcription-PCR clearly documented the presence of IFN-beta but not of IFN-alpha transcripts in RNA from bone marrow-derived macrophages (BMM). Culture of bone marrow cells for 7 days in the presence of macrophage colony-stimulating factor plus IL-4 or treatment of mature BMM with IL-4 for 3 to 4 days resulted in pronounced inhibition of IFN-beta transcript levels. As a consequence, BMM became highly permissive to viral infection and induction of the IFN-responsive 2',5'-oligoadenylate synthetase was inhibited. In view of the evidence for low-level constitutive secretion of IFN in vivo, it is possible that IL-4 influences the host's antiviral defense system.

摘要

我们发现,白细胞介素-4(IL-4)可消除小鼠巨噬细胞中组成型β干扰素(IFN-β)的合成。通过逆转录聚合酶链反应(RT-PCR)对内源性IFN mRNA进行分析,清楚地证明了来自骨髓来源巨噬细胞(BMM)的RNA中存在IFN-β转录本,但不存在IFN-α转录本。在巨噬细胞集落刺激因子加IL-4存在的情况下,将骨髓细胞培养7天,或用IL-4处理成熟BMM 3至4天,都会导致IFN-β转录水平明显受到抑制。结果,BMM对病毒感染变得高度敏感,并且对IFN反应性2',5'-寡腺苷酸合成酶的诱导也受到抑制。鉴于体内存在低水平组成型IFN分泌的证据,IL-4有可能影响宿主的抗病毒防御系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1876/237099/1ab03a8cddcd/jvirol00019-0640-a.jpg

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