TY - JOUR
T1 - Identification and quantification of plasma calciprotein particles with distinct physical properties in patients with chronic kidney disease
AU - Miura, Yutaka
AU - Iwazu, Yoshitaka
AU - Shiizaki, Kazuhiro
AU - Akimoto, Tetsu
AU - Kotani, Kazuhiko
AU - Kurabayashi, Masahiko
AU - Kurosu, Hiroshi
AU - Kuro-O, Makoto
N1 - Funding Information:
We thank Ms. Yuko Shimizu (Jichi Medical University) for technical assistance, Dr. Akira Hasegawa and Dr. Daisuke Nagata for helping clinical studies, Ms. Johanne Pastor, Prof. Orson Moe, and Prof. Charles Pak (University of Texas Southwestern Medical Center, U.S.A.) for their supports at the early phase of this study. This work was supported in part by AMED-CREST, AMED, JSPS KAKENHI Grant Number JP16H05302, and grant from Bristol-Myers Squibb Foundation.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Calciprotein particles (CPP) are solid-phase calcium-phosphate bound to serum protein fetuin-A and dispersed as colloids in the blood. Recent clinical studies indicated that serum CPP levels were increased with decline of renal function and associated with inflammation and vascular calcification. However, CPP assays used in these studies measured only a part of CPP over a certain particle size and density. Here we show that such CPP are mostly artifacts generated during processing of serum samples in vitro. The native CPP in fresh plasma are smaller in size and lower in density than those artifactual CPP, composed of fetuin-A carrying amorphous and/or crystalline calcium-phosphate, and increased primarily with serum phosphate levels. We have identified several physicochemical factors that promote aggregation/dissolution of CPP and transition of the calcium-phosphate from the amorphous phase to the crystalline phase in vitro, including addition of anti-coagulants, composition of buffer for sample dilution, the number of freeze-thaw cycles, the speed for sample freezing, and how many hours the samples were left at what temperature. Therefore, it is of critical importance to standardize these factors during sample preparation in clinical studies on CPP and to investigate the biological activity of the native CPP.
AB - Calciprotein particles (CPP) are solid-phase calcium-phosphate bound to serum protein fetuin-A and dispersed as colloids in the blood. Recent clinical studies indicated that serum CPP levels were increased with decline of renal function and associated with inflammation and vascular calcification. However, CPP assays used in these studies measured only a part of CPP over a certain particle size and density. Here we show that such CPP are mostly artifacts generated during processing of serum samples in vitro. The native CPP in fresh plasma are smaller in size and lower in density than those artifactual CPP, composed of fetuin-A carrying amorphous and/or crystalline calcium-phosphate, and increased primarily with serum phosphate levels. We have identified several physicochemical factors that promote aggregation/dissolution of CPP and transition of the calcium-phosphate from the amorphous phase to the crystalline phase in vitro, including addition of anti-coagulants, composition of buffer for sample dilution, the number of freeze-thaw cycles, the speed for sample freezing, and how many hours the samples were left at what temperature. Therefore, it is of critical importance to standardize these factors during sample preparation in clinical studies on CPP and to investigate the biological activity of the native CPP.
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U2 - 10.1038/s41598-018-19677-4
DO - 10.1038/s41598-018-19677-4
M3 - Article
C2 - 29352150
AN - SCOPUS:85040807876
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 1256
ER -