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Pathogenic uromodulin mutations result in premature intracellular polymerization

Author:
Stewart, Andrew P., Sandford, Richard N., Karet Frankl, Fiona E., Edwardson, J. Michael
Source:
FEBS letters 2015 v.589 pp. 89-93
ISSN:
0014-5793
Subject:
atomic force microscopy, biopsy, genes, image analysis, kidney diseases, mutants, mutation, patients, polymerization, proteins, urine
Abstract:
Several renal diseases involve mutations in the gene encoding uromodulin, the predominant protein in urine. We investigated the intracellular processing of wild-type uromodulin, and three mutants: p.V93_G97del/ins AASC; C155R; and C150S. A renal biopsy from a patient harboring the C155R mutation revealed intracellular protein accumulation. Wild-type uromodulin was efficiently trafficked to the cell surface in transfected tsA 201 cells, whereas the mutants were partially retained within the cell, and incompletely processed. Atomic force microscopy imaging revealed that the intracellular mutant proteins contained fibrillar structures similar to urinary uromodulin. We suggest that premature intracellular polymerization underlies the pathology of uromodulin diseases.
Agid:
5393004