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缓激肽对正常大鼠肾细胞密度依赖性生长抑制丧失的影响。

Effect of bradykinin on loss of density-dependent growth inhibition of normal rat kidney cells.

作者信息

Lahaye D H, Afink G B, Bleijs D A, Van Alewijk D C, Van Zoelen E J

机构信息

Department of Cell Biology, University of Nijmegen, Faculty of Science, The Netherlands.

出版信息

Cell Mol Biol (Noisy-le-grand). 1994 Jul;40(5):717-21.

PMID:7981625
Abstract

Normal rat kidney fibroblasts, density-arrested in the presence of epidermal growth factor (EGF), can be restimulated to proliferate in a synchronous way and acquire a transformed phenotype following treatment with additional growth factors like retinoic acid (RA) and transforming growth factor (TGF)-beta. It was found that bradykinin has a strong inhibitory effect on growth stimulation induced by these factors, an effect which cannot be mimicked by PGF2 alpha. The growth-inhibiting effect can be blocked by inhibitors of cyclo-oxygenase activity, indicating that the relevant second messenger is most likely a prostaglandin. Externally added PGJ2, at a concentration of 10 microM, can mimic the inhibitory effect of bradykinin on the loss of density-arrest induced by RA suggesting that PGJ2 is a possible candidate for being the bradykinin induced growth-inhibiting prostaglandin.

摘要

在表皮生长因子(EGF)存在的情况下达到密度抑制的正常大鼠肾成纤维细胞,在用视黄酸(RA)和转化生长因子(TGF)-β等其他生长因子处理后,可被重新刺激以同步方式增殖并获得转化表型。研究发现,缓激肽对这些因子诱导的生长刺激具有强烈的抑制作用,而这种作用不能被前列腺素F2α模拟。环氧化酶活性抑制剂可阻断这种生长抑制作用,这表明相关的第二信使很可能是一种前列腺素。以10微摩尔/升的浓度外源性添加PGJ2,可模拟缓激肽对RA诱导的密度抑制丧失的抑制作用,这表明PGJ2可能是缓激肽诱导的生长抑制性前列腺素的候选物质。

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