Iron inhibits hydroxyapatite crystal growth in vitro

被引:76
作者
Guggenbuhl, Pascal [1 ,2 ]
Filmon, Robert [1 ]
Mabilleau, Guillaume [1 ]
Basle, Michel F. [1 ]
Chappard, Daniel [1 ]
机构
[1] INSERM, Fac Med, LHEA, U 922, F-49045 Angers, France
[2] CHU, Hop Sud, Serv Rhumatol, F-35203 Rennes, France
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2008年 / 57卷 / 07期
关键词
D O I
10.1016/j.metabol.2008.02.004
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Hemochromatosis is a known cause of osteoporosis in which the pathophysiology of bone loss is largely unknown and the role of iron remains questionable. We have investigated the effects of iron on the growth of hydroxyapatite crystals in vitro on carboxymethylated poly(2-hydroxyethyl methacrylate) pellets. This noncellular and enzyme-independent model mimics the calcification of woven bone (composed of calcospherites made of hydroxyapatite crystals). Polymer pellets were incubated with body fluid containing iron at increasing concentrations (20, 40, 60 mu mol/L). Hydroxyapatite growth was studied by chemical analysis, scanning electron microscopy, and Raman microscopy. When incubated in body fluid containing iron, significant differences were observed with control pellets. Iron was detected at a concentration of 5.41- to 7.16-fold that of controls. In pellets incubated with iron, there was a similar to 3- to 4-fold decrease of Ca and P and a similar to 1.3- to 1.4-fold increase in the Ca/P ratio. There was no significant difference among the iron groups of pellets, but a trend to a decrease of Ca with the increase of iron concentration was noted. Calcospheilte diameters were significantly lower on pellets incubated with iron. Raman microspectroscopy showed a decrease in crystallinity (measured by the full width of the half height of the 960 Delta cm(-1) band) with a significant increase in carbonate substitution (measured by the intensity ratio of 1071 to 960 Delta cm(-1) band). Energy dispersive x-ray analysis identified iron in the calcospherites. In vitro, iron is capable to inhibit bone crystal growth with significant changes in crystallinity and carbonate substitution. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:903 / 910
页数:8
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