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肿瘤坏死因子可诱导人成纤维细胞合成两种蛋白质。

Tumor necrosis factor induces synthesis of two proteins in human fibroblasts.

作者信息

Kirstein M, Baglioni C

出版信息

J Biol Chem. 1986 Jul 25;261(21):9565-7.

PMID:3733684
Abstract

Human fibroblasts were insensitive to tumor necrosis factor (TNF) alone but were killed when treated with TNF together with the inhibitor of protein synthesis cycloheximide. However, incubation with TNF before addition of cycloheximide protected these cells from cytotoxicity. This suggested that TNF induced some protective mechanism(s) and that protein synthesis was required for this induction. By labeling fibroblasts with [35S]methionine, we observed that TNF induced in these cells the synthesis of two proteins of Mr 36,000 and 42,000 (p36 and p42). This induction was dependent on the TNF concentration and was observed within a few hours after addition of TNF. Actinomycin D prevented synthesis of these proteins, suggesting that TNF induced transcription of the corresponding mRNAs. p42 appeared to be stable, whereas p36 turned over within a few hours. The physiological role of these proteins in the cellular response to TNF remains to be established.

摘要

人成纤维细胞单独对肿瘤坏死因子(TNF)不敏感,但在与蛋白质合成抑制剂环己酰亚胺一起处理时会被杀死。然而,在添加环己酰亚胺之前用TNF孵育可保护这些细胞免受细胞毒性。这表明TNF诱导了一些保护机制,并且这种诱导需要蛋白质合成。通过用[35S]甲硫氨酸标记成纤维细胞,我们观察到TNF在这些细胞中诱导了两种分子量分别为36,000和42,000的蛋白质(p36和p42)的合成。这种诱导依赖于TNF浓度,并且在添加TNF后的几个小时内就可以观察到。放线菌素D阻止了这些蛋白质的合成,表明TNF诱导了相应mRNA的转录。p42似乎是稳定的,而p36在几个小时内就会周转。这些蛋白质在细胞对TNF的反应中的生理作用仍有待确定。

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