vertebral body;
age development;
collagen/mineral composite;
mineral particles;
scanning-SAXS;
backscattered electron imaging;
histomorphometry;
mineralization density distribution;
D O I:
10.1006/jsbi.2001.4427
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:
Knowledge of the structural development of the human vertebrae from non-weight-bearing before birth to weight-bearing after birth is still poor. We studied the mineralized tissue of the developing lumbar L4 vertebral body at ages 15 weeks postconception to 97 years from the tissue level (trabecular architecture) to the material level (micro- and nanostructure). Trabecular architecture was investigated by 2D histomorphometry and the material level was examined by quantitative backscattered electron imaging (for typical calcium content, CaMaxFreq) and scanning small-angle X-ray scattering (for mean mineral particle thickness). During early development, the trabecular orientation changed from a radial to a vertical/horizontal pattern. For bone area per tissue area and trabecular width in postnatal cancellous bone, the maximum was reached at adolescence (20 years), while for trabecular number the maximum was reached at childhood (approximate to1 year). CaMaxFreq was lower in early bone (approximate to21 wt%) than in mineralized cartilage (approximate to29 wt%) and adolescent bone (approximate to23 wt%). In conclusion, the changes at the tissue level were observed to continue throughout life while the development of bone at the material level (CaMaxFreq, mineral particle thickness and orientation) is essentially complete after the first years of life. CaMaxFreq and mean particle thickness increase rapidly during the first years and reach saturation. Remarkably, when these parameters are plotted versus logarithm of age, they appear linear. (C) 2001 Elsevier Science (USA).
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
FRATZL, P
FRATZLZELMAN, N
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HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
FRATZLZELMAN, N
KLAUSHOFER, K
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机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
KLAUSHOFER, K
VOGL, G
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HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
VOGL, G
KOLLER, K
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机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
FRATZL, P
FRATZLZELMAN, N
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h-index: 0
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
FRATZLZELMAN, N
KLAUSHOFER, K
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h-index: 0
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
KLAUSHOFER, K
VOGL, G
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h-index: 0
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA
VOGL, G
KOLLER, K
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h-index: 0
机构:
HANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIAHANUSCH HOSP,DEPT MED 4,LUDWIG BOLTZMANN RES UNIT CLIN & EXPT OSTEOL,A-1140 VIENNA,AUSTRIA