PUBLICATION

Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis

Authors
Lane, B.M., Chryst-Stangl, M., Wu, G., Shalaby, M., El Desoky, S., Middleton, C.C., Huggins, K., Sood, A., Ochoa, A., Malone, A.F., Vancini, R., Miller, S.E., Hall, G., Kim, S.Y., Howell, D.N., Kari, J.A., Gbadegesin, R.
ID
ZDB-PUB-211211-4
Date
2021
Source
JCI insight   7(2): (Journal)
Registered Authors
Keywords
Chronic kidney disease, Genetic diseases, Monogenic diseases, Nephrology
MeSH Terms
  • Adrenal Cortex Hormones
  • Apoptosis/drug effects
  • CRISPR-Cas Systems/genetics
  • Carrier Proteins/genetics*
  • Cells, Cultured
  • Endocytosis*/drug effects
  • Endocytosis*/genetics
  • Gene Knockout Techniques
  • Genetic Association Studies
  • High-Throughput Nucleotide Sequencing/methods
  • Humans
  • Nephrotic Syndrome*/drug therapy
  • Nephrotic Syndrome*/genetics
  • Nephrotic Syndrome*/metabolism
  • Nephrotic Syndrome*/pathology
  • Oxidative Stress*/drug effects
  • Oxidative Stress*/genetics
  • Podocytes*/drug effects
  • Podocytes*/metabolism
  • Reactive Oxygen Species/antagonists & inhibitors
PubMed
34874915 Full text @ JCI Insight
Abstract
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 three 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 can 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 SSNS patients. The p.H310Y variant also disrupts binding of clavesin-1 to alpha-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, this data identifies CLVS1 as a candidate gene for SSNS, provides insight into therapeutic effects of corticosteroids on podocyte cellular dynamics and adds to the growing evidence on the importance of endocytosis and oxidative stress regulation to podocyte function.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping