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α-干扰素、β-干扰素和γ-干扰素可提高腹膜巨噬细胞中核糖体RNA前体的水平,但对巨噬细胞系和成纤维细胞则无此作用。

Interferon-alpha, -beta, and -gamma augment the levels of rRNA precursors in peritoneal macrophages but not in macrophage cell lines and fibroblasts.

作者信息

Radzioch D, Clayton M, Varesio L

出版信息

J Immunol. 1987 Aug 1;139(3):805-12.

PMID:2439593
Abstract

We have studied the ribosomal RNA content in murine peritoneal macrophages activated to cytotoxicity with interferon-alpha (IFN-alpha), interferon-beta (IFN-beta), and interferon-gamma (IFN-gamma). Total RNA was purified from IFN-alpha, -beta, or -gamma activated macrophages, and Northern blot analysis was performed by using subcloned fragments specific for precursor rRNA (pre-rRNA) as probes. All types of interferon (alpha, beta, gamma) at the doses normalized for induction of cytotoxic activity caused accumulation of 45S, 41S, and 36S pre-rRNA. In contrast, the levels of 32S pre-RNA and 28S, 5.8S, and 18S mature rRNA were not affected by IFN treatment. Therefore, the accumulation of pre-rRNA in macrophages activated to cytotoxicity by IFN was not paralleled by changes in total content of mature rRNA. No accumulation of pre-rRNA upon IFN treatment was found in a murine fibroblast cell line (L929 cells) or in a macrophage cell line (GG2EE) immortalized from bone marrow of C3H/HeJ mice. Neither of those cell lines become cytotoxic in response to IFN. Overall, our data support the concept that IFN acts selectively on the mechanism controlling the levels of some pre-rRNA and that the mechanism of IFN action involves the post-transcriptional control of ribosomal gene expression.

摘要

我们研究了用α干扰素(IFN-α)、β干扰素(IFN-β)和γ干扰素(IFN-γ)激活至细胞毒性的小鼠腹腔巨噬细胞中的核糖体RNA含量。从经IFN-α、-β或-γ激活的巨噬细胞中纯化总RNA,并使用针对前体rRNA(pre-rRNA)的亚克隆片段作为探针进行Northern印迹分析。所有类型的干扰素(α、β、γ)在标准化为诱导细胞毒性活性的剂量下,都会导致45S、41S和36S pre-rRNA的积累。相比之下,32S pre-RNA以及28S、5.8S和18S成熟rRNA的水平不受IFN处理的影响。因此,经IFN激活至细胞毒性的巨噬细胞中pre-rRNA的积累与成熟rRNA总含量的变化并不平行。在小鼠成纤维细胞系(L929细胞)或从C3H/HeJ小鼠骨髓永生化的巨噬细胞系(GG2EE)中,未发现IFN处理后pre-rRNA的积累。这两种细胞系均不会因IFN而产生细胞毒性。总体而言,我们的数据支持以下概念:IFN选择性作用于控制某些pre-rRNA水平的机制,且IFN的作用机制涉及核糖体基因表达的转录后控制。

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