In situ examination of the time-course for secondary mineralization of Haversian bone using synchrotron Fourier transform infrared micro spectroscopy

被引:53
作者
Fuchs, Robyn K. [1 ,2 ]
Allen, Matt R. [2 ]
Ruppel, Meghan E. [3 ]
Diab, Tamim [2 ]
Phipps, Roger J. [4 ]
Miller, Lisa M. [5 ]
Burr, David B. [2 ,6 ]
机构
[1] Indiana Univ, Dept Phys Therapy, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[3] SUNY Stony Brook, Dept Biomed Engn, Stony Brook, NY 11794 USA
[4] Procter & Gamble Pharmaceut, Mason, OH USA
[5] Brookhaven Natl Lab, Upton, NY 11973 USA
[6] Indiana Univ, Sch Med, Dept Orthopaed Surg, Indianapolis, IN USA
关键词
secondary mineralization; primary mineralization; FTIRM; cortical bone; animal model; carbonate; phosphate;
D O I
10.1016/j.matbio.2007.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
At the tissue level it is well established that the rate of remodeling is related to the degree of mineralization. However, it is unknown how long it takes for an individual bone structural unit (BSU) to become fully mineralized during secondary mineralization. Using synchrotron Fourier transform infrared microspectroscopy (FTIRM) we examined the time required for newly formed bone matrix to reach a physiological mineralization limit. Twenty-six, four-month old female New Zealand white rabbits were administered up to four different fluorochrome labels at specific time points to evaluate the chemical composition of labeled osteons from the tibial diaphysis that had mineralized for 1, 8, 18, 35, 70, 105, 140, 175, 210, 245, 280, 315, 350, and 385 days. Interstitial bone from 505 day old rabbits was used as a reference value for the physiological limit to which bone mineralizes. Using synchrotron FTIRM, area integrations were carried out on protein (Amide I: 1688-1623 cm(-1)), carbonate (v(2)CO(3)(2-): 905-825 cm(-1)), and phosphate (v(4)PO(4)(3-): 650-500 cm(-1)) IR bands. IR spectral data are presented as ratios of phosphate/protein (overall matrix mineralization) and carbonate/protein. The rate of mineralization of osteonal bone proceeded rapidly between day I and 18, reaching 67% of interstitial bone levels. This was followed by a slower, more progressive accumulation of mineral up to day 350. By 350 days the rate of increase plateaued. The ratio of carbonate/protein also increased rapidly during the first 18 days, reaching 73% of interstitial bone levels. The ratio of carbonate/protein plateaued by day 315, reaching levels not significantly different to interstitial bone levels. In conclusion, our data demonstrate that bone accumulates mineral rapidly during the first 18 days (primary mineralization), followed by a more gradual increase in the accumulation of mineral (secondary mineralization) which we found to be completed in 350 days. (C) 2007 Elsevier B.V./International Society of Matrix Biology. All rights reserved.
引用
收藏
页码:34 / 41
页数:8
相关论文
共 52 条
[1]   Aging of microstructural compartments in human compact bone [J].
Akkus, O ;
Polyakova-Akkus, A ;
Adar, F ;
Schaffler, MB .
JOURNAL OF BONE AND MINERAL RESEARCH, 2003, 18 (06) :1012-1019
[2]  
AMPRINO R, 1952, ACTA ANAT, V15, P1
[3]   Optimal methods for processing mineralized tissues for Fourier transform infrared microspectroscopy [J].
Aparicio, S ;
Doty, SB ;
Camacho, NP ;
Paschalis, EP ;
Spevak, L ;
Mendelsohn, R ;
Boskey, AL .
CALCIFIED TISSUE INTERNATIONAL, 2002, 70 (05) :422-429
[4]  
BARBOS MP, 1983, ACTA ANAT, V115, P178
[5]   The degree of mineralization of bone tissue measured by computerized quantitative contact microradiography [J].
Boivin, G ;
Meunier, PJ .
CALCIFIED TISSUE INTERNATIONAL, 2002, 70 (06) :503-511
[6]   Changes in bone remodeling rate influence the degree of mineralization of bone [J].
Boivin, G ;
Meunier, PJ .
CONNECTIVE TISSUE RESEARCH, 2002, 43 (2-3) :535-537
[7]   Infrared spectroscopic characterization of mineralized tissues [J].
Boskey, AL ;
Mendelsohn, R .
VIBRATIONAL SPECTROSCOPY, 2005, 38 (1-2) :107-114
[8]   Rapid establishment of chemical and mechanical properties during lamellar bone formation [J].
Busa, B ;
Miller, L ;
Rubin, C ;
Qin, YX ;
Judex, S .
CALCIFIED TISSUE INTERNATIONAL, 2005, 77 (06) :386-394
[9]   PERFORMANCE OF AN INFRARED MICROSPECTROMETER AT THE NSLS [J].
CARR, GL ;
REFFNER, JA ;
WILLIAMS, GP .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1995, 66 (02) :1490-1492
[10]   Poorly crystalline apatites: evolution and maturation in vitro and in vivo [J].
Cazalbou, S ;
Combes, C ;
Eichert, D ;
Rey, C ;
Glimcher, MJ .
JOURNAL OF BONE AND MINERAL METABOLISM, 2004, 22 (04) :310-317