Pattaranit Ratchada, van den Berg Hugo Antonius, Spanswick David
MOAC Doctoral Training Centre, University of Warwick, Coventry, UK.
Sci Prog. 2008;91(Pt 3):285-316. doi: 10.3184/003685008X361343.
Diabetes is a common endocrine disorder, primarily characterised by elevated plasma glucose levels. The disease affects all age groups worldwide. Most patients suffer from Type 2 diabetes, which is mainly due to insulin resistance. It is thought that changes in insulin signalling pathways underlie the development of insulin resistance. This article aims to review recent studies that have elucidated the role of individual proteins in these insulin signalling pathways. These studies have been undertaken using two strategies, one employing mice carrying a global null mutation of particular gene-encoding proteins by the homologous recombination method and another strategy using mice with tissue-specific insulin receptor and/or GLUT4 knockout by the Cre-loxP system. The various phenotypes of these knockout mice, and the light they shed on the etiology of insulin resistance, are discussed. By advancing our understanding of the complex molecular mechanisms underlying insulin resistance, these knock-out models may help us to develop more effective treatments for Type 2 diabetes.
糖尿病是一种常见的内分泌疾病,主要特征为血糖水平升高。该疾病影响全球所有年龄组。大多数患者患有2型糖尿病,这主要是由于胰岛素抵抗。人们认为胰岛素信号通路的变化是胰岛素抵抗发生的基础。本文旨在综述近期阐明单个蛋白质在这些胰岛素信号通路中作用的研究。这些研究采用了两种策略,一种是通过同源重组方法培育携带特定基因编码蛋白的全身性无效突变的小鼠,另一种策略是使用通过Cre-loxP系统构建的具有组织特异性胰岛素受体和/或GLUT4基因敲除的小鼠。本文讨论了这些基因敲除小鼠的各种表型,以及它们对胰岛素抵抗病因的启示。通过增进我们对胰岛素抵抗潜在复杂分子机制的理解,这些基因敲除模型可能有助于我们开发出更有效的2型糖尿病治疗方法。