PUBLICATION
Kif21a deficiency leads to impaired glomerular filtration barrier function
- Authors
- Riedmann, H., Kayser, S., Helmstädter, M., Epting, D., Bergmann, C.
- ID
- ZDB-PUB-231107-6
- Date
- 2023
- Source
- Scientific Reports 13: 1916119161 (Journal)
- Registered Authors
- Bergmann, Carsten, Epting, Daniel
- Keywords
- none
- MeSH Terms
-
- Kidney Glomerulus/metabolism
- Proteinuria/metabolism
- Animals
- Zebrafish
- Podocytes*/metabolism
- Glomerular Filtration Barrier*
- PubMed
- 37932480 Full text @ Sci. Rep.
Citation
Riedmann, H., Kayser, S., Helmstädter, M., Epting, D., Bergmann, C. (2023) Kif21a deficiency leads to impaired glomerular filtration barrier function. Scientific Reports. 13:1916119161.
Abstract
The renal glomerulus represents the major filtration body of the vertebrate nephron and is responsible for urine production and a number of other functions such as metabolic waste elimination and the regulation of water, electrolyte and acid-base balance. Podocytes are highly specialized epithelial cells that form a crucial part of the glomerular filtration barrier (GFB) by establishing a slit diaphragm for semipermeable plasma ultrafiltration. Defects of the GFB lead to proteinuria and impaired kidney function often resulting in end-stage renal failure. Although significant knowledge has been acquired in recent years, many aspects in podocyte biology are still incompletely understood. By using zebrafish as a vertebrate in vivo model, we report a novel role of the Kinesin-like motor protein Kif21a in glomerular filtration. Our studies demonstrate specific Kif21a localization to the podocytes. Its deficiency resulted in altered podocyte morphology leading to podocyte foot process effacement and altered slit diaphragm formation. Finally, we proved considerable functional consequences of Kif21a deficiency by demonstrating a leaky GFB resulting in severe proteinuria. Conclusively, our data identified a novel role of Kif21a for proper GFB function and adds another piece to the understanding of podocyte architecture and regulation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping