Key result
NOSTRIN gene knockdown in zebrafish induces proteinuria by altering glomerular filtration barrier function.
Why the study?
Does knockdown of the NOSTRIN gene alter glomerular barrier function in zebrafish?
Does knockdown of the NOSTRIN gene alter glomerular barrier function in zebrafish?
The hypertension-associated gene NOSTRIN is essential for glomerular filtration barrier integrity, suggesting its alteration may contribute to podocyte disease and proteinuria.
NOSTRIN knockdown may link hypertension genes to proteinuria; hypothesis-generating in zebrafish, human relevance remains open.
Hypertension is one of the major risk factors for chronic kidney disease. Using quantitative trait loci analysis, we identified the gene of the F-BAR protein NOSTRIN in the center of an overlapping region in rat and human quantitative trait loci that are associated with hypertension. Immunohistochemical analysis revealed a predominantly podocytic expression pattern of NOSTRIN in human and mouse glomeruli. Further, NOSTRIN colocalizes with cell-cell contact-associated proteins β-catenin and zonula occludens-1 and interacts with the slit-membrane-associated adaptor protein CD2AP. In zebrafish larvae, knockdown of nostrin alters the glomerular filtration barrier function, inducing proteinuria and leading to ultrastructural morphological changes on the endothelial and epithelial side and of the glomerular basement membrane of the glomerular capillary loop. We conclude that NOSTRIN expression is an important factor for the integrity of the glomerular filtration barrier. Disease-related alteration of NOSTRIN expression may not only affect the vascular endothelium and, therefore, contribute to endothelial cell dysfunction but might also contribute to the development of podocyte disease and proteinuria.
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Kirsch et al. (2013) studied Hypertension and chronic kidney disease. Knockdown of nostrin was evaluated on Glomerular filtration barrier function (proteinuria and ultrastructural morphological changes). Knockdown of the NOSTRIN gene in zebrafish larvae altered glomerular filtration barrier function, inducing proteinuria and ultrastructural morphological changes.
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