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Proteoglycan core protein in human urine and its possible role on calcium oxalate urolithiasis
Author(s) -
Yoshimura Kazuhiro,
Miyake Osamu,
Tsujihata Masao,
Yoshioka Toshiaki,
Yamaguchi Seiji,
Koide Takuo,
Takahara Shiro,
Okuyama Akihiko
Publication year - 1999
Publication title -
international journal of urology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.172
H-Index - 67
eISSN - 1442-2042
pISSN - 0919-8172
DOI - 10.1046/j.1442-2042.1999.611107.x
Subject(s) - medicine , calcium oxalate , urine , proteoglycan , calcium , core protein , oxalate , core (optical fiber) , anatomy , virology , chemistry , cartilage , materials science , organic chemistry , composite material
Background: There are only a few papers reporting on the role of proteoglycan core protein in calcium oxalate stone formation. The present study was carried out to investigate the role of core protein of proteoglycan in human urine on calcium oxalate (CaOx) crystallization.Methods: Proteoglycans were collected from whole human urine. The covalently bound glycosaminoglycans (GAG) of proteoglycans were then digested by GAG lyase. The inhibitory activity on CaOx crystal growth in vitro was measured before and after enzyme digestion of proteoglycans. Sodium dodecylsulfate–polyacrylamide gel electrophoresis (SDS‐PAGE) of the core protein of proteoglycans and the analysis of amino acid sequence were performed.Results: The core protein showed significant inhibitory activity on CaOx crystal growth, which scarcely changed when compared with that of proteoglycans before enzyme digestion. The SDS‐PAGE revealed that the core protein was a single unit with a molecular weight of 26 kDa and amino acid sequencing demonstrated high homology to interalpha‐trypsin inhibitor (ITI) light chain (bikunin) with Kunitz inhibitor domain as a core protein.Conclusions: The results suggested that human urine contains proteoglycans and a major part of them is ITI light chain (bikunin). The Kunitz inhibitor domain, a core protein of bikunin, has significant inhibitory activity on CaOx crystallization without GAG bound covalently to the core protein.