Division of Nephrology and Hypertension, Department of Medicine, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Kidney Int. 2012 Jun;81(11):1053-5. doi: 10.1038/ki.2012.12.
Our concept of the kidney filtration barrier is changing from one of a static sieve into one of a highly dynamic structure regulated through the motility of podocyte foot processes. Inactivation of the small GTPase RhoA in vitro causes hypermotility, whereas activation decreases motility. Wang et al. show that both overactivation and underactivation of RhoA lead to podocyte foot process effacement and proteinuria in vivo. These data suggest that podocyte health requires a well-controlled balance between the two extremes.
我们对肾脏滤过屏障的认识正从静态筛网的概念转变为高度动态的结构,该结构通过足细胞足突的运动来调节。体外抑制小 GTP 酶 RhoA 可导致其过度活跃,而激活则会降低其活性。Wang 等人发现,RhoA 的过度激活和失活均会导致体内足细胞足突融合和蛋白尿。这些数据表明,足细胞的健康需要在这两个极端之间保持良好的平衡。