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成纤维细胞前胶原生成的调节。转化生长因子-β1通过一种对百日咳毒素敏感的G蛋白诱导前列腺素E2生成,但不诱导前胶原合成。

Regulation of fibroblast procollagen production. Transforming growth factor-beta 1 induces prostaglandin E2 but not procollagen synthesis via a pertussis toxin-sensitive G-protein.

作者信息

McAnulty R J, Chambers R C, Laurent G J

机构信息

Department of Medicine, University College London Medical School, U.K.

出版信息

Biochem J. 1995 Apr 1;307 ( Pt 1)(Pt 1):63-8. doi: 10.1042/bj3070063.

Abstract

Transforming growth factor-beta 1 (TGF beta 1) initiates a series of signalling events resulting in diverse cellular responses including stimulation of extracellular matrix protein production. In this study we have investigated the role of pertussis toxin-sensitive G-proteins in mediating the effects of TGF beta 1 on fibroblast procollagen metabolism. TGF beta 1 stimulated human fetal lung fibroblast procollagen synthesis and production in a dose-dependent manner which was maximal at 0.5 ng/ml. TGF beta 1 also decreased the proportion of newly synthesized procollagen degraded intracellularly. Pertussis toxin, a G-protein inhibitor, further stimulated TGF beta 1-induced procollagen synthesis and production, but alone it had no effect on fibroblast procollagen metabolism. Addition of indomethacin also potentiated the TGF beta 1-induced increase in procollagen synthesis and production. The effects of pertussis toxin and indomethacin were not additive. Pertussis toxin and indomethacin did not affect the proportion of newly synthesized procollagen degraded intracellularly, either alone or in combination, by control cells. The TGF beta 1-induced decrease in intracellular procollagen degradation was maintained but not further affected by pertussis toxin or indomethacin. TGF beta 1 increased prostaglandin E2 (PGE2) compared with PGE2 production by control cells. Addition of pertussis toxin or indomethacin blocked the TGF beta 1-induced increase in PGE2 production. The TGF beta 1-induced increase in PGE2 preceded the increase in procollagen production. These results demonstrate that TGF beta 1-induced procollagen synthesis by lung fibroblasts is modulated by production of PGE2. Pertussis toxin and indomethacin block the production of PGE2 and enhance the effect of TGF beta 1 on procollagen synthesis. From these data we conclude that the effects of TGF beta 1 on PGE2 production but not procollagen synthesis are mediated via a receptor linked to a pertussis toxin-sensitive G-protein.

摘要

转化生长因子-β1(TGF-β1)引发一系列信号事件,导致多种细胞反应,包括刺激细胞外基质蛋白的产生。在本研究中,我们研究了百日咳毒素敏感的G蛋白在介导TGF-β1对成纤维细胞前胶原代谢作用中的作用。TGF-β1以剂量依赖的方式刺激人胎儿肺成纤维细胞前胶原的合成和产生,在0.5 ng/ml时达到最大值。TGF-β1还降低了细胞内新合成的前胶原被降解的比例。G蛋白抑制剂百日咳毒素进一步刺激TGF-β1诱导的前胶原合成和产生,但单独使用时对成纤维细胞前胶原代谢没有影响。添加吲哚美辛也增强了TGF-β1诱导的前胶原合成和产生增加。百日咳毒素和吲哚美辛的作用不是相加的。百日咳毒素和吲哚美辛单独或联合使用时,对对照细胞内新合成的前胶原被降解的比例没有影响。TGF-β1诱导的细胞内前胶原降解减少得以维持,但不受百日咳毒素或吲哚美辛的进一步影响。与对照细胞产生的前列腺素E2(PGE2)相比,TGF-β1增加了PGE2的产生。添加百日咳毒素或吲哚美辛可阻断TGF-β1诱导的PGE2产生增加。TGF-β1诱导的PGE2增加先于前胶原产生的增加。这些结果表明,肺成纤维细胞中TGF-β1诱导的前胶原合成受PGE2产生的调节。百日咳毒素和吲哚美辛阻断PGE2的产生并增强TGF-β1对前胶原合成的作用。从这些数据我们得出结论,TGF-β1对PGE2产生而非前胶原合成的作用是通过与百日咳毒素敏感的G蛋白相连的受体介导的。

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