首页> 外文OA文献 >Changes in inositol lipids and phosphates after stimulation of the MAS-transfected NG115-401L-C3 cell line by mitogenic and non-mitogenic stimuli.
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Changes in inositol lipids and phosphates after stimulation of the MAS-transfected NG115-401L-C3 cell line by mitogenic and non-mitogenic stimuli.

机译:有丝分裂和非有丝分裂刺激刺激MAS转染的NG115-401L-C3细胞系后肌醇脂质和磷酸盐的变化。

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摘要

A neuronal cell line (NG115-401L-C3) was stimulated by mitogenic (angiotensin) and non-mitogenic (bradykinin) peptides and examined for the time course of changes in the levels of radiolabelled inositol phosphates and phospholipids. Both peptides stimulated the time-dependent production of Ins(1,4,5)P3 and related metabolites. Bradykinin caused a much larger increase in Ins(1,4,5)P3 than did angiotensin. However, both peptides stimulated similar rises in the levels of Ins(1,3,4)P3 and InsP4. Bradykinin, but not angiotensin, caused a rapid (within 2 s) fall in the levels of PtdIns(4,5)P2 and PtdIns(4)P. Serum pretreatment of the cells caused a 2-3-fold potentiation of both the responses to bradykinin and angiotensin. Although significant levels of PtdIns(3)P were detected in resting cells, neither mitogenic (angiotensin, insulin-like growth factor I, transforming growth factor beta) nor non-mitogenic (bradykinin, nerve growth factor, interleukin-1) receptor activation changed its levels, arguing against regulation of either PtdIns 3-kinase or PtdIns(3)P phosphatase. We conclude that, as judged by the levels of its product. PtdIns(3)P, the enzyme PtdIns 3-kinase is not activated. This questions the significance of this activity in the receptor-mediated initiation of DNA synthesis.
机译:有丝分裂(血管紧张素)和非有丝分裂(缓激肽)肽刺激神经元细胞系(NG115-401L-C3),并检查放射性标记的肌醇磷酸酯和磷脂水平变化的时间过程。两种肽均刺激了Ins(1,4,5)P3及其相关代谢产物的时间依赖性产生。缓激肽引起的Ins(1,4,5)P3的增加比血管紧张素引起的大得多。但是,这两种肽均刺激Ins(1,3,4)P3和InsP4的水平出现类似的上升。缓激肽而非血管紧张素导致PtdIns(4,5)P2和PtdIns(4)P的水平迅速下降(在2 s内)。血清对细胞的预处理导致对缓激肽和血管紧张素的反应都增强了2至3倍。尽管在静息细胞中检测到显着水平的PtdIns(3)P,有丝分裂(血管紧张素,胰岛素样生长因子I,转化生长因子β)和非有丝分裂(缓激肽,神经生长因子,白介素-1)受体激活均未改变其水平,反对对PtdIns 3-激酶或PtdIns(3)P磷酸酶的调节。我们得出结论,根据其产品水平来判断。 PtdIns(3)P,PtdIns 3-激酶未激活。这质疑了这种活性在受体介导的DNA合成起始中的重要性。

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