Origin of the pattern of trabecular bone: an experiment and a model.

As a result of an experiment in which the development of a mineral phase in the rabbit embryo was observed, a model is proposed to explain the mechanism that controls the place of precipitation of crystals in mineralizing tissue. The reaction-diffusion equations for the specified compounds are formulated and solved. Among a variety of compounds the concentrations of carbon dioxide, oxygen, HCO-3 ions, H+ ions, calcium, and inorganic phosphorus are evaluated. CO2, HCO-3 ions, and H+ ions, are distinguished due to their key role in the maintenance of the pH value. The local concentration of oxygen is the pivot factor that controls the metabolic rate, i.e., production of CO2. Next the supersaturation was estimated on the basis of the calculated values of pH and the concentrations of calcium and inorganic phosphorus. It is assumed that the synthesis of the organic matrix breaks the metastable equilibrium with respect to spontaneous precipitation and leads to the deposition of minerals. It was found that the geometry of the vasculature determines the shape of primitive trabecular bone (woven bone) while the value of the diffusion coefficient may be the key factor indicating the possibility of mineralization under the control of a living organism.

[1]  G. H. Nancollas,et al.  Crystal growth of calcium phosphates - epitaxial considerations , 1981 .

[2]  C. Stanford,et al.  Calcium and phosphate supplementation promotes bone cell mineralization: implications for hydroxyapatite (HA)-enhanced bone formation. , 2000, Journal of biomedical materials research.

[3]  J. Ross,et al.  Measurements of the solubilities and dissolution rates of several hydroxyapatites. , 2002, Biomaterials.

[4]  P. Hauschka,et al.  Nucleation and inhibition of hydroxyapatite formation by mineralized tissue proteins. , 1996, The Biochemical journal.

[5]  P. Tracqui,et al.  A physiological view of in vivo calcium dynamics: the regulation of a nonlinear self-organized system. , 1989, Bone.

[6]  W. E. Brown,et al.  Thermodynamics of apatite crystal growth and dissolution , 1981 .

[7]  A. Boskey Amorphous Calcium Phosphate: The Contention of Bone , 1997, Journal of dental research.

[8]  G. Mundy Factors which stimulate bone growth in vivo. , 1993, Growth regulation.

[9]  Glimcher Mj The possible role of collagen fibrils and collagen-phosphoprotein complexes in the calcification of bone in vitro and in vivo. , 1990 .

[10]  J. Fox,et al.  Metastable Equilibrium Solubility Behavior of Bone Mineral , 1999, Calcified Tissue International.

[11]  G. Karsenty Bone formation and factors affecting this process. , 2000, Matrix biology : journal of the International Society for Matrix Biology.

[12]  R. Soloway,et al.  Inhibition of calcium hydroxyapatite formation by polyamines. , 2008, Liver.

[13]  M. Lafage-Proust,et al.  Relationships between trabecular bone remodeling and bone vascularization: a quantitative study. , 2002, Bone.

[14]  E. P. Katz The kinetics of mineralization in vitro. I. The nucleation properties of 640-Å collagen at 25° , 1969 .

[15]  J. Staub,et al.  Spatio-temporal self-organization of bone mineral metabolism and trabecular structure of primary bone , 1995, Acta biotheoretica.

[16]  W. Landis,et al.  Mineral characterization in calcifying tissues: atomic, molecular and macromolecular perspectives. , 1996, Connective tissue research.

[17]  H. Madsen,et al.  Precipitation of calcium phosphate at 40° C from neutral solution , 1991 .

[18]  A. Boskey Biomineralization: Conflicts, challenges, and opportunities , 1998, Journal of cellular biochemistry.

[19]  G. Vereecke,et al.  Calculation of the Solubility Diagrams in the System Ca(oh)2-h3po4-koh-hno3-co2-h2o , 1990 .