Abstract
Polymeric IgA (pIgA) is transcytosed by the pIgA receptor (pIgR) across mucosal epithelial cells. After transcytosis to the apical surface, the extracellular, ligand-binding portion of the pIgR is proteolytically cleaved. A missense mutation in human pIgR, A580V, is associated with IgA nephropathy and nasopharyngeal carcinoma. We report that this mutation reduces the rate of transcytosis of pIgR and pIgA, and seemingly the rate of pIgR cleavage. We propose that the defects in pIgR trafficking caused by the A580V mutation may underlie the pathogenesis of both diseases.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Cell Line, Tumor
-
Dogs
-
Glomerulonephritis, IGA / genetics
-
Glomerulonephritis, IGA / metabolism*
-
Glomerulonephritis, IGA / pathology
-
Humans
-
Immunoglobulin A / genetics
-
Immunoglobulin A / metabolism*
-
Mutation, Missense
-
Nasopharyngeal Neoplasms / genetics
-
Nasopharyngeal Neoplasms / metabolism*
-
Nasopharyngeal Neoplasms / pathology
-
Neoplasm Proteins / genetics
-
Neoplasm Proteins / metabolism*
-
Protein Transport / genetics
-
Proteolysis
-
Receptors, Polymeric Immunoglobulin / genetics
-
Receptors, Polymeric Immunoglobulin / metabolism*
-
Transcytosis*
Substances
-
Immunoglobulin A
-
Neoplasm Proteins
-
Receptors, Polymeric Immunoglobulin