Kluge Reinhart, Scherneck Stephan, Schürmann Annette, Joost Hans-Georg
Max-Rubner-Laboratory, German Institute of Human Nutrition Potsdam-Rehbrücke, Nuthetal, Germany.
Methods Mol Biol. 2012;933:59-73. doi: 10.1007/978-1-62703-068-7_5.
The New Zealand Obese (NZO) mouse is one of the most thoroughly investigated polygenic models for the human metabolic syndrome and type 2 diabetes. It presents the main characteristics of the disease complex, including early-onset obesity, insulin resistance, dyslipidemia, and hypertension. As a consequence of this syndrome, a combination of lipotoxicity and glucotoxicity produces beta-cell failure and apoptosis resulting in hypoinsulinemia and diabetic hyperglycemia. With NZO as a breeding partner, several adipogenic and diabetogenic gene variants have been identified by hypothesis-free positional cloning (Tbc1d1, Zfp69) or by combining genetic screens and candidate gene approaches (Pctp, Abcg1, Nmur2, Lepr). This chapter summarizes the present knowledge of the NZO strain and describes its pathophysiology as well as the known underlying genetic defects.
新西兰肥胖(NZO)小鼠是针对人类代谢综合征和2型糖尿病研究最为深入的多基因模型之一。它呈现出该疾病复合体的主要特征,包括早发性肥胖、胰岛素抵抗、血脂异常和高血压。作为这种综合征的结果,脂毒性和糖毒性共同作用导致β细胞功能衰竭和凋亡,进而引发低胰岛素血症和糖尿病性高血糖。以NZO作为繁殖伙伴,通过无假设定位克隆(Tbc1d1、Zfp69)或结合基因筛选与候选基因方法(Pctp、Abcg1、Nmur2、Lepr),已鉴定出几种致肥胖和致糖尿病的基因变体。本章总结了目前关于NZO品系的知识,并描述了其病理生理学以及已知的潜在遗传缺陷。