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Mathematical modeling of the insulin signal transduction pathway for prediction of insulin sensitivity from expression data

机译:胰岛素信号转导途径的数学建模,可根据表达数据预测胰岛素敏感性

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Mathematical models of biological pathways facilitate a systems biology approach to medicine. However, these models need to be updated to reflect the latest available knowledge of the underlying pathways. We developed a mathematical model of the insulin signal transduction pathway by expanding the last major previously reported model and incorporating pathway components elucidated since the original model was reported. Furthermore, we show that inputting gene expression data of key components of the insulin signal transduction pathway leads to sensible predictions of glucose clearance rates in agreement with reported clinical measurements. In one set of simulations, our model predicted that glycerol kinase knockout mice have reduced GLUT4 translocation, and consequently, reduced glucose uptake. Additionally, a comparison of our extended model with the original model showed that the added pathway components improve simulations of glucose clearance rates. We anticipate this expanded model to be a useful tool for predicting insulin sensitivity in mammalian tissues with altered expression protein phosphorylation or mRNA levels of insulin signal transduction pathway components. (C) 2014 Elsevier Inc. All rights reserved.
机译:生物途径的数学模型促进了医学的系统生物学方法。但是,需要更新这些模型以反映有关基础途径的最新可用知识。我们通过扩展最后一个以前报道的主要模型并合并自报道原始模型以来阐明的途径成分,开发了胰岛素信号传导途径的数学模型。此外,我们表明输入胰岛素信号转导途径的关键组成部分的基因表达数据可导致对糖清除率的合理预测,与已报道的临床测量结果一致。在一组模拟中,我们的模型预测甘油激酶敲除小鼠的GLUT4易位减少,因此葡萄糖摄取减少。此外,我们扩展模型与原始模型的比较表明,增加的途径成分改善了葡萄糖清除率的模拟。我们预计该扩展模型将成为预测哺乳动物组织中胰岛素表达改变的表达蛋白磷酸化或mRNA水平的胰岛素信号转导途径组分的有用工具。 (C)2014 Elsevier Inc.保留所有权利。

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