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Modeling of feedback interactions between map kinase and cAMP signaling pathways

机译:地图激酶与阵营信号通路之间的反馈相互作用建模

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Both the mitogen-activated protein kinase (MAPK) and cAMP signaling pathways play critical roles in cellular responses to external stimuli. Although many molecular interactions between these pathways have been identified, little is known about how such interactions shape the signals transmitted through these pathways. Here I present a theoretical model incorporating known feedback interactions between the MAPK and cAMP signaling pathways. In contrast to previous studies considering only the MAPK cascade, simulations made using this model suggest that, in the presence of feedback regulation from the cAMP signaling pathway, elements of the MAPK cascade do not necessarily behave in a bistable fashion. Rather, under constant stimulus conditions, interactions between these pathways can trigger slow oscillatory responses. Undoubtedly, other feedback interactions not considered here further influence both signaling pathways. Given the large number of interactions between MAPK, cAMP, and other signaling pathways (e.g., Ca{sup}(2+)), it seems likely that oscillations in one pathway will trigger oscillations in several others. However, until better in vivo methods are developed for measuring enzyme activity and second messenger concentrations, we will be only be able to consider how information might be encoded within such oscillations.
机译:丝裂原激活的蛋白激酶(MAPK)和CAMP信号通路均在对外部刺激的细胞反应中起重要作用。尽管已经鉴定了这些途径之间的许多分子相互作用,但是关于这种相互作用如何形状通过这些途径传输的信号而少知。这里我介绍了一种理论模型,其结合了MAPK和CAMP信号传导途径之间的已知反馈相互作用。与以前的研究相比,考虑到MAPK级联,使用该模型进行的模拟表明,在从营地信号通路的反馈调节存在下,MAPK级联的元素不一定以双稳态方式行事。相反,在恒定刺激条件下,这些途径之间的相互作用可以触发缓慢的振荡反应。毫无疑问,这里不考虑的其他反馈相互作用进一步影响信号传导途径。鉴于MAPK,CAMP和其他信令路径之间的大量交互(例如,CA {SUP}(2+)),似乎在一个路径中振荡将触发其他几个轨道。然而,直到为测量酶活性和第二个信使浓度而开发更好的体内方法,我们将只能考虑如何在这种振荡中编码信息。

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