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血小板源性生长因子BB对血小板源性生长因子α受体和β受体mRNA及蛋白的诱导作用

Induction of platelet-derived growth factor alpha- and beta-receptor mRNA and protein by platelet-derived growth factor BB.

作者信息

Eriksson A, Nistér M, Leveen P, Westermark B, Heldin C H, Claesson-Welsh L

机构信息

Ludwig Institute for Cancer Research, Biomedical Center, Uppsala, Sweden.

出版信息

J Biol Chem. 1991 Nov 5;266(31):21138-44.

PMID:1657951
Abstract

We describe that stimulation of human fibroblasts with platelet-derived growth factor BB (PDGF-BB) induces a transient up-regulation of the PDGF alpha- and beta-receptor transcript and protein levels. The effect of PDGF-BB on the receptor transcript levels was more pronounced than those seen when other cytokines were used. Regulation of transcript levels by PDGF-BB was mediated through post-transcriptional mechanisms. No induction could be observed in a nuclear run-on analysis, but cycloheximide treatment attenuated the accumulation of both alpha- and beta-receptor transcripts induced by PDGF-BB. An increase in receptor protein levels was observed using two different experimental approaches. Increased amounts of receptor precursor forms could be immunoprecipitated from metabolically labeled cells, stimulated with PDGF-BB. In a second approach, cells were exposed to different concentrations of PDGF-BB, and, in a subsequent step, ligand binding analysis was performed. In this experiment, an initial down-regulation of receptors was followed by increased levels of the cell surface forms of the receptors. In conclusion, PDGF-BB, but not PDGF-AA, induces increased synthesis of both PDGF alpha- and beta-receptor protein; this constitutes a positive feed-back mechanism, which, for example, could serve to potentiate autocrine stimulation of growth.

摘要

我们描述了用血小板衍生生长因子BB(PDGF-BB)刺激人成纤维细胞会诱导PDGFα受体和β受体转录本及蛋白水平的短暂上调。与使用其他细胞因子时相比,PDGF-BB对受体转录本水平的影响更为显著。PDGF-BB对转录本水平的调节是通过转录后机制介导的。在核转录分析中未观察到诱导作用,但放线菌酮处理减弱了PDGF-BB诱导的α受体和β受体转录本的积累。使用两种不同的实验方法观察到了受体蛋白水平的增加。从用PDGF-BB刺激的经代谢标记的细胞中可以免疫沉淀出增加量的受体前体形式。在第二种方法中,将细胞暴露于不同浓度的PDGF-BB,随后进行配体结合分析。在该实验中,受体最初下调,随后细胞表面形式的受体水平增加。总之,PDGF-BB而非PDGF-AA可诱导PDGFα受体和β受体蛋白的合成增加;这构成了一种正反馈机制,例如可用于增强生长的自分泌刺激。

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