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Proteome of Human Calcium Kidney Stones

Authors
Canales, Benjamin K.Anderson, LorraineHiggins, LeeAnnEnsrud-Bowlin, KathyRoberts, Ken P.Wu, BaolinKim, Il WonMonga, Manoj
Issue Date
Oct-2010
Publisher
ELSEVIER SCIENCE INC
Citation
UROLOGY, v.76, no.4
Journal Title
UROLOGY
Volume
76
Number
4
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/14651
DOI
10.1016/j.urology.2010.05.005
ISSN
0090-4295
Abstract
OBJECTIVES Idiopathic calcium oxalate (CaOx) stones are believed to develop attached to papillary subepithelial deposits called Randall's plaques. Calcium phosphate (CaP) stones, conversely, are thought to arise within the inner medullary collecting ducts, enlarging and damaging surround tubular structures as they expand. If this is true, we theorize that differences will be seen within the organic portion (matrix) of CaOx stones compared with CaP stones using a mass spectroscopy (MS) approach. METHODS From a cohort of 47 powdered stones, 25 calculi (13 CaOx, 12 CaP) were confirmed to contain a dominant mineral content of >80% by powder x-ray diffraction. Matrix proteins were then extracted, purified, and digested. Peptide tandem MS data were acquired, and spectra were searched against a large human protein database to identify protein matches. RESULTS No significant differences were seen between pattern profiles of CaOx and CaP stones. However, variations in protein expression patterns were seen within individual CaOx (monohydrate and dihydrate) and CaP (apatite and brushite) mineral subtypes, suggesting a relationship between crystal-surface binding properties and matrix composition. Both groups contain a large number of inflammatory proteins and a catalog of common proteins is included. CONCLUSIONS Calcium kidney stone matrix contains hundreds of proteins and is predominated by proteins associated with inflammatory response. Many of the same proteins were identified in both CaOx and CaP stones, suggesting inflammation as a unifying origin or a common secondary role in calcium stone pathogenesis. UROLOGY 76: 1017.e13-1017.e20, 2010. (C) 2010 Elsevier Inc.
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