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缓激肽诱导成纤维细胞和神经母细胞瘤细胞中肌醇1,4,5 -三磷酸的生成:百日咳毒素、细胞外钙及蛋白激酶C下调的影响

Bradykinin-induced generation of inositol 1,4,5-trisphosphate in fibroblasts and neuroblastoma cells: effect of pertussis toxin, extracellular calcium, and down-regulation of protein kinase C.

作者信息

Fu T, Okano Y, Nozawa Y

机构信息

Department of Biochemistry, Gifu University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Dec 30;157(3):1429-35. doi: 10.1016/s0006-291x(88)81035-0.

Abstract

The net content of inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] was measured in bradykinin (BK)-stimulated NIH3T3 fibroblasts and neuroblastoma-glioma hybrid cells (NG108-15). BK-mediated production of Ins(1,4,5)P3 was not affected by replacing the medium with Ca2+-free medium, but addition of EGTA (1mM) to Ca2+-free medium markedly prevented production of Ins(1,4,5)P3. Although pertussis toxin (PT) treatment caused ADP-ribosylation in both NIH3T3 cells and NG108-15 cells, the BK-induced Ins(1,4,5)P3 formation was considerably reduced in the former cells but not in the latter cells, suggesting that PT-sensitive and PT-insensitive GTP-binding proteins are involved in phosphoinositide phospholipase C (PI-PLC) activation in fibroblasts and neuroblastoma cells, respectively. In NG108-15 cells down-regulated in protein kinase C (PKC) by long-term exposure to phorbol 12-myristate 13-acetate (PMA), BK-stimulated Ins(1,4,5)P3 accumulation was significantly enhanced compared to control cells.

摘要

在缓激肽(BK)刺激的NIH3T3成纤维细胞和神经母细胞瘤-胶质瘤杂交细胞(NG108-15)中测量了肌醇1,4,5-三磷酸[Ins(1,4,5)P3]的净含量。用无钙培养基替换培养基不会影响BK介导的Ins(1,4,5)P3生成,但向无钙培养基中添加EGTA(1mM)可显著抑制Ins(1,4,5)P3的生成。尽管百日咳毒素(PT)处理会导致NIH3T3细胞和NG108-15细胞均发生ADP-核糖基化,但BK诱导的Ins(1,4,5)P3形成在前者细胞中显著减少,而在后者细胞中未减少,这表明PT敏感和PT不敏感的GTP结合蛋白分别参与成纤维细胞和神经母细胞瘤细胞中磷酸肌醇磷脂酶C(PI-PLC)的激活。在长期暴露于佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)而使蛋白激酶C(PKC)下调的NG108-15细胞中,与对照细胞相比,BK刺激的Ins(1,4,5)P3积累显著增强。

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