Accili D, Kido Y, Nakae J, Lauro D, Park B C
Naomi Berrie Diabetes Center, Department of Medicine, College of Physicians & Surgeons of Columbia University, New York, NY 10032, USA.
Curr Mol Med. 2001 Mar;1(1):9-23. doi: 10.2174/1566524013364040.
Diabetes affects millions of people worldwide, and its chronic complications are a leading cause of death in many industrialized countries. In a minority of patients, diabetes is brought about by the auto-immune destruction of insulin-producing pancreatic beta cells (Type 1 diabetes). In the vast majority of patients, diabetes is brought about by a combination of genetic and environmental factors that affect the organism's ability to respond to insulin (Type 2 diabetes). This impairment is due to a complex abnormality involving insulin action at the periphery and insulin production in the beta cell. Genetic factors play a key role in the development of type 2 diabetes. However, the inheritance of diabetes is non-Mendelian in nature, due to genetic heterogeneity, polygenic pathogenesis and incomplete penetrance. For these reasons, many laboratories have developed "designer" mice bearing targeted mutations in genes of the insulin action and insulin secretion pathways in order to develop a better model for the inheritance and pathogenesis of type 2 diabetes. These mutant mice are beginning to challenge established paradigms in the pathogenesis of type 2 diabetes and to shed light onto the genetic interactions underlying its complex inheritance. Here we review recent progress in the field and assess its impact on human studies of the genetics, prevention and treatment of type 2 diabetes.
糖尿病影响着全球数百万人,其慢性并发症是许多工业化国家的主要死因。在少数患者中,糖尿病是由产生胰岛素的胰腺β细胞的自身免疫性破坏引起的(1型糖尿病)。在绝大多数患者中,糖尿病是由影响机体对胰岛素反应能力的遗传和环境因素共同作用引起的(2型糖尿病)。这种损害是由于涉及外周胰岛素作用和β细胞胰岛素产生的复杂异常所致。遗传因素在2型糖尿病的发生发展中起关键作用。然而,由于遗传异质性、多基因发病机制和不完全外显率,糖尿病的遗传是非孟德尔式的。出于这些原因,许多实验室已经培育出在胰岛素作用和胰岛素分泌途径基因中带有靶向突变的“设计”小鼠,以便为2型糖尿病的遗传和发病机制建立更好的模型。这些突变小鼠开始挑战2型糖尿病发病机制中的既定范式,并揭示其复杂遗传背后的基因相互作用。在此,我们综述该领域的最新进展,并评估其对2型糖尿病遗传学、预防和治疗人类研究的影响。