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环磷酸腺苷刺激盘基网柄菌中肌醇三磷酸的积累。

Cyclic AMP stimulates accumulation of inositol trisphosphate in Dictyostelium.

作者信息

Europe-Finner G N, Newell P C

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

J Cell Sci. 1987 Mar;87 ( Pt 2):221-9. doi: 10.1242/jcs.87.2.221.

Abstract

Previous studies indicated that in Dictyostelium amoebae signal transmission from cell surface cyclic AMP receptors to intracellular events concerned with chemotaxis involves inositol 1,4,5-trisphosphate (1,4,5-IP3): micromolar amounts of 1,4,5-IP3 or Ca2+ were found to mimic the effects of chemoattractants and 1,4,5-IP3 triggered release of Ca2+ from non-mitochondrial stores. Here we report a more direct test of the involvement of inositol phosphates. Intact amoebae were labelled with high specific activity [3H]inositol, then stimulated with the chemoattractant cyclic AMP at 22 degrees C and rapidly assayed for phosphorylated inositol products formed. Labelled IP3 was found to accumulate transiently after a pulse of 50 nM-cyclic AMP, with a peak at 15 s after stimulation and some (inconclusive) evidence for a more rapidly formed peak at 5 s or less. Inositol bisphosphate (IP2) showed a transient shallow peak at about 20 s. When the events of signal transmission were slowed down by incubation at 4 degrees C, the rapidly formed IP3 peak could be consistently seen at 5 s after stimulation and the second peak at 25-30 s. Further resolution of the IP3 peaks indicated the presence of IP4, which represented a major fraction of the peak accumulated at 5 s (4 degrees C). The results provide an important link in the chain of evidence connecting the cell surface cyclic AMP receptors, via IP3, with the Ca2+-activated events of chemotaxis.

摘要

先前的研究表明,在盘基网柄菌变形虫中,从细胞表面环磷酸腺苷(cAMP)受体到与趋化性相关的细胞内事件的信号传递涉及肌醇1,4,5-三磷酸(1,4,5-IP3):发现微摩尔量的1,4,5-IP3或Ca2+可模拟趋化剂的作用,并且1,4,5-IP3触发了Ca2+从非线粒体储存库中的释放。在此,我们报告了一项关于肌醇磷酸参与情况的更直接测试。完整的变形虫用高比活度的[3H]肌醇进行标记,然后在22℃下用趋化剂环磷酸腺苷刺激,并快速测定形成的磷酸化肌醇产物。发现标记的IP3在50 nM-环磷酸腺苷脉冲后短暂积累,刺激后15秒达到峰值,并且有一些(不确定的)证据表明在5秒或更短时间有一个形成更快的峰值。肌醇二磷酸(IP2)在约20秒时出现一个短暂的浅峰。当在4℃下孵育使信号传递事件减慢时,在刺激后5秒可始终观察到快速形成的IP3峰值,第二个峰值在25 - 30秒出现。对IP3峰值的进一步解析表明存在IP4,它占4℃下5秒积累峰值的主要部分。这些结果在将细胞表面环磷酸腺苷受体通过IP3与趋化性的Ca2+激活事件联系起来的证据链中提供了一个重要环节。

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