Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06520, USA.
J Cell Biol. 2010 Nov 15;191(4):701-10. doi: 10.1083/jcb.201006173.
Polycystic kidney disease is a common genetic disorder in which fluid-filled cysts displace normal renal tubules. Here we focus on autosomal dominant polycystic kidney disease, which is attributable to mutations in the PKD1 and PKD2 genes and which is characterized by perturbations of renal epithelial cell growth control, fluid transport, and morphogenesis. The mechanisms that connect the underlying genetic defects to disease pathogenesis are poorly understood, but their exploration is shedding new light on interesting cell biological processes and suggesting novel therapeutic targets.
多囊肾病是一种常见的遗传性疾病,其中充满液体的囊肿取代了正常的肾小管。在这里,我们重点关注常染色体显性多囊肾病,它归因于 PKD1 和 PKD2 基因突变,并以肾脏上皮细胞生长控制、液体转运和形态发生的改变为特征。将潜在的遗传缺陷与疾病发病机制联系起来的机制还了解甚少,但对它们的探索正在为有趣的细胞生物学过程提供新的认识,并为新的治疗靶点提供线索。