Department of Pediatrics, Division of Nephrology, and Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Pediatric Department, Pediatric Nephrology Center of Excellence, King Abdulaziz University, Jeddah, Saudi Arabia.
JCI Insight. 2022 Jan 25;7(2):e152102. doi: 10.1172/jci.insight.152102.
We performed next-generation sequencing in patients with familial steroid-sensitive nephrotic syndrome (SSNS) and identified a homozygous segregating variant (p.H310Y) in the gene encoding clavesin-1 (CLVS1) in a consanguineous family with 3 affected individuals. Knockdown of the clavesin gene in zebrafish (clvs2) produced edema phenotypes due to disruption of podocyte structure and loss of glomerular filtration barrier integrity that could be rescued by WT CLVS1 but not the p.H310Y variant. Analysis of cultured human podocytes with CRISPR/Cas9-mediated CLVS1 knockout or homozygous H310Y knockin revealed deficits in clathrin-mediated endocytosis and increased susceptibility to apoptosis that could be rescued with corticosteroid treatment, mimicking the steroid responsiveness observed in patients with SSNS. The p.H310Y variant also disrupted binding of clavesin-1 to α-tocopherol transfer protein, resulting in increased reactive oxygen species (ROS) accumulation in CLVS1-deficient podocytes. Treatment of CLVS1-knockout or homozygous H310Y-knockin podocytes with pharmacological ROS inhibitors restored viability to control levels. Taken together, these data identify CLVS1 as a candidate gene for SSNS, provide insight into therapeutic effects of corticosteroids on podocyte cellular dynamics, and add to the growing evidence of the importance of endocytosis and oxidative stress regulation to podocyte function.
我们对患有家族性类固醇敏感性肾病综合征 (SSNS) 的患者进行了下一代测序,并在一个有 3 名受影响个体的近亲家族中发现了编码 clavesin-1 (CLVS1) 的基因中的纯合子分离变异 (p.H310Y)。在斑马鱼中敲低 clavesin 基因 (clvs2) 会因足细胞结构破坏和肾小球滤过屏障完整性丧失而产生水肿表型,而 WT CLVS1 可以挽救,但 p.H310Y 变体则不能。用 CRISPR/Cas9 介导的 CLVS1 敲除或纯合 H310Y 敲入分析培养的人足细胞,发现内吞作用的网格蛋白介导缺陷和对细胞凋亡的敏感性增加,这可以用皮质类固醇治疗挽救,模拟 SSNS 患者观察到的类固醇反应性。p.H310Y 变体还破坏了 clavesin-1 与 α-生育酚转移蛋白的结合,导致 CLVS1 缺陷足细胞中活性氧 (ROS) 积累增加。用药理学 ROS 抑制剂处理 CLVS1 敲除或纯合 H310Y 敲入的足细胞可将细胞活力恢复至对照水平。总之,这些数据将 CLVS1 确定为 SSNS 的候选基因,深入了解皮质类固醇对足细胞细胞动力学的治疗作用,并增加了内吞作用和氧化应激调节对足细胞功能重要性的日益增多的证据。