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In vitro precipitation of calcium phosphate under intracellular conditions: formation of brushite from an amorphous precursor in the absence of ATP

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Summary

Release of mitochondrial calcium has been shown to occur concomitant with mineral ion loading of matrix vesicles at the onset of mineralization in epiphyseal growth plate cartilage. Matrix vesicles contain amorphous calcium phosphate (ACP), a mineral form that usually results from rapid precipitation at high initial levels of Ca2+ and/or inorganic P (Pi). Since the cytosol of growth plate chondrocytes has been found to contain high levels of Pi, rapid release of mitochondrial Ca2+ into the cytosol may causelocal precipitation of calcium phosphate and thus be coupled with matrix vesicle formation. Studies were carried out to determine the kinetics and nature of mineral formation that occur when small amounts of Ca2+ are added under various conditions to a Pi buffer composed of electrolytes matched in concentrations and pH to that of the cytosol of epiphyseal chondrocytes. Depending on the manner in which Ca2+ was added, ACP, dicalcium phosphate dihyrate (DCPD), or apatite (HA) first formed. In the presence of ATP, ACP was the only solid phase detected, being stable for at least 24 h. However, in its absence, ACP rapidly transformed into DCPD, Increasing the pH of the reaction buffer from 6.9 to 7.5 increased the amount of ACP initially formed, but DCPD was consistently found upon ACP transformation. Yet at pH 8.0, ACP persisted for at least 24 h. The amount of precipitate formed was proportional to the level of added Ca2+; precipitates formed when as little as 1.0 mmole was added per liter of buffer.

Our findings support thepossibility that rapid release of mitochondrial Ca2+ may cause localized intracellular precipitation of ACP. Since nascent ACP is known to stimulate membrane fusion and blebbing of vesicles, these findings may explain the presence of ACP in matrix vesicles. The rapid conversion of ACP to DCPD in the absence of ATP under these conditions may also explain the reported occurrence of DCPD in samples of early mineralizing tissue.

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References

  1. Matthews JL, Martin JH (1971) Intracellular transport of calcium and its relationship to homeostasis and mineralization. Am J Med 50:589–597

    Article  PubMed  CAS  Google Scholar 

  2. Martin JH, Matthews JL (1970) Mitochondrial granules in chondrocytes, osteoblasts and osteocytes. Clin Orthop Rel Res 68:273–278

    CAS  Google Scholar 

  3. Brighton CT, Hunt RM (1976) Histochemical localization of calcium in growth plate mitochondria and matrix vesicles. Fed Proc 35:143–147

    PubMed  CAS  Google Scholar 

  4. Brighton CT, Hunt RM (1976) Electron microscopic pyroantimonate studies of matrix vesicles and mitochondria in rachitic growth plate. Metab Bone Dis Rel Res 1:199–204

    Article  Google Scholar 

  5. Anderson HC (1969) Vesicles associated with calcification in the matrix of epiphyseal cartilage. J Cell Biol 41:59–72

    Article  PubMed  CAS  Google Scholar 

  6. Bonucci E (1970) Fine structure and histochemistry of “calcifying globules” in epiphyseal cartilage. Z Zellforsch Mikrosk Anat 103:192–217

    Article  PubMed  CAS  Google Scholar 

  7. Ali SY, Sajdera SW, Anderson HC (1970) Isolation and characterization of calcifying matrix vesicles from epiphyseal cartilage. Proc Natl Acad Sci USA 67:1513–1520

    Article  PubMed  CAS  Google Scholar 

  8. Eisenman DR, Glick PL (1972) Ultrastructure of initial crystal formation in dentin. J Ultrastruct Res 41:18–28

    Article  Google Scholar 

  9. Felix R, Herrmann W, Fleisch H (1978) Stimulation of precipitation of calcium phosphate by matrix vesicles. Biochem J 170:681–691

    PubMed  CAS  Google Scholar 

  10. Wuthier RE (1977) Electrolytes of isolated epiphyseal chondrocytes. matrix vesicles and extracellular fluid. Calif Tissue Res 23:125–139

    Article  CAS  Google Scholar 

  11. Wuthier RE, Gore ST (1977) Partition of inorganic ions and phospholipids in isolated cell, membrane and matrix vesicle fractions: Evidence for Ca-Pi-acidic phospholipid complexes. Calcif Tissue Res 24:163–171

    Article  PubMed  CAS  Google Scholar 

  12. Warner GP (1981) Calcium phosphate metabolism by matrix vesicles from chicken epiphyseal cartilage. PhD Thesis, Univ of S Carolina, Columbia, pp 51–54

    Google Scholar 

  13. Zakai N, Kulka RG, Loyter A (1977) Membrane ultrastructural changes during calcium phosphate-induced fusion of human erythrocyte ghosts. Proc Natl Acad Sci USA 74:2417–2421

    Article  PubMed  CAS  Google Scholar 

  14. Majumdar S, Baker RF (1980) Phosphate-calcium induced fusion of chicken erythrocytes. Exp Cell Res 126:175–182

    Article  PubMed  CAS  Google Scholar 

  15. Fraley R, Wilschut J, Düzgünes N, Smith C, Papahadjapoulos (1980) Studies on the mechanism of membrane fusion: role of phosphate in promoting calcium-induced fusion of phospholipid vesicles. Biochemistry 19:6021–6029

    Article  PubMed  CAS  Google Scholar 

  16. Wuthier RE (1981) Proposed mechanism of matrix vesicle formation and vesicle-mediated mineralization. In: Ascenzi A, Bonucci E, de Bernard B (eds) Matrix vesicles, Wichtig Editore, Milano, pp 103–109

    Google Scholar 

  17. Wuthier RE (1982) A review of the primary mechanism of endochondral calcification with special emphasis on the role of cells, mitochondria and matrix vesicles. Clin Orthop Rel Res 169:219–242

    CAS  Google Scholar 

  18. Herzfeld J, Roufosse A, Haberkorn RA, Griffin RA, Glimcher MJ (1980) Magic angle sample spinning in inhomogeneously broadened biological systems. Phil Trans R Soc Lond B 289:459–469

    CAS  Google Scholar 

  19. Roufosse AH, Landis WJ, Sabine WK, Glimcher MJ (1979) Identification of brushite in newly deposited bone mineral from embryonic chicks. J Ultrastruct Res 68:235–255

    Article  PubMed  CAS  Google Scholar 

  20. Betts FC, Trotta R, Goldberg MR, Posner AS (1979) Nonapatite mineral in actively calcifying tissues. Orthopaed Trans 3:201

    Google Scholar 

  21. LeGeros RZ, Legeros JP, Trautz OR, Klein E (1970) Spectral properties of carbonate-containing apatites. Develop Appl Spectr 7B:3–12

    Google Scholar 

  22. Wuthier RE, Eanes ED (1975) Effect of phospholipids on the transformation of amorphous calcium phosphate to hydroxyapatitein vitro. Calcif Tiss Res 19:197–210

    CAS  Google Scholar 

  23. Rouser G, Siakotos AN, Fleischer S (1966) Quantitative analysis of phospholipids by thin-layer chromatography and phosphorus analysis of spots. Lipids 1:85–86

    Article  CAS  PubMed  Google Scholar 

  24. Davies CW (1962) Ion association. Butterworths, London

    Google Scholar 

  25. Nancollas GH, Tomažič B (1974) Growth of calcium phosphate on hydroxyapatite crystals. Effect of supersaturation and ionic medium. J Physical Chem 78:2218–2224

    Article  CAS  Google Scholar 

  26. Nancollas, GH (1982) Phase transformation during precipitation of calcium salts. In: Nancollas GH (ed) Biological mineralization and demineralization. Springer-Verlag, Berlin, pp 79–99

    Google Scholar 

  27. Shapiro IM, Golub EE, Kakuta S, Hazelgrove J, Havery J, Chance B, Frasca P (1982) Initiation of endochondral calcification is related to changes in the redox state of hypertrophic chondrocytes. Science 217:950–952

    Article  PubMed  CAS  Google Scholar 

  28. Klee CB, Crouch TH, Richman PG (1980) Calmodulin. Ann Rev Biochem 49:489–515

    Article  PubMed  CAS  Google Scholar 

  29. Lam Y-F, Lin AK-LC, Ho C (1979) A phosphorus-31 nuclear magnetic resonance investigation of intracellular environment in human normal and sickle cell blood. Blood 54:196–209

    PubMed  CAS  Google Scholar 

  30. Burt CT, Glonek T, Barany M (1976) Analysis of phosphate metabolites in the intracellular pH, and the state of adenosine triphosphate in intact muscle by phosphorus nuclear magnetic resonance. J Biol Chem 251:2584–2591

    PubMed  CAS  Google Scholar 

  31. Shapiro IM, Golub EE, May M, Rabinowitz JL (1983) Studies of nucleotides of growth-plate cartilage. Evidence linking changes in cellular metabolism with cartilage calcification. Bioscience Reports 3:345–351

    Article  PubMed  CAS  Google Scholar 

  32. Hubbard HL (1984) Characterization of the extracellular fluid of chicken epiphyseal growth plate cartilage: Studies on metabolites and electrolytes. PhD Thesis, University of South Carolina, pp 95–121

  33. Bygrave FL (1982) Calcium transport in mitochondria isolated from normal and iniured tissues. In: Anghileri LJ, Tuffet-Anghileri AM (eds) The role of calcium in biological systems, vol. I. CRC Press, Boca Raton, FL, pp 85–93

    Google Scholar 

  34. Hamaguchi Y (1982) Intracellular measurement of free calcium. In: Anghileri LJ, Tuffet-Anghileri AM (eds) The role of calcium in biological systems, vol. I. CRC Press, Boca Raton, FL, pp 85–93

    Google Scholar 

  35. McCormick LH, Borden FY (1974) The occurence of aluminum phosphate precipitate in plant roots. Soil Sci Soc Am Proc 38:931–934

    Article  CAS  Google Scholar 

  36. Waisel Y, Hoffen A, Eshel A (1970) The localization of aluminum in cortex cells of bean and barley root by x-ray microanalysis. Physiol Plant 23:75–79

    Article  CAS  Google Scholar 

  37. Malone C, Koeppe DE, Miller RJ (1974) Localization of lead accumulated by corn plants. Plant Physiol 53:388–394

    Article  PubMed  CAS  Google Scholar 

  38. Cheng P-T, Pritzker KPH (1983) Solution Ca/P ratio affects calcium phosphate crystal phases. Calcif Tissue Int 35:596–601

    Article  PubMed  CAS  Google Scholar 

  39. Blumenthal NC, Betts FC, Posner AS (1975) Nucleotide stabilization of amorphous calcium phosphate. Mat Res Bull 10:1055–1060

    Article  CAS  Google Scholar 

  40. Blumenthal NC, Betts FC, Posner AS (1977) Stabilization of amorphous calcium phosphate by Mg and ATP. Calcif Tissue Res 23:245–250

    Article  PubMed  CAS  Google Scholar 

  41. Boskey AL, Posner AS (1974) Magnesium stabilization of amorphous calcium phosphate: a kinetic study. Mat Res Bull 9:907–916

    Article  CAS  Google Scholar 

  42. Termine JD, Peckauskas RA, Posner AS (1970) Calcium phosphate formationin vitro. II. Effects of environment on amorphous-crystalline transformation. Arch Biochem Biophys 140:318–325

    Article  PubMed  CAS  Google Scholar 

  43. Strates BS, Neuman WF, Levinskas GJ (1957) The solubility of bone mineral. I. Precipitation in near neutral solutions of calcium and phosphate. J Phys Chem 61:279–282

    Article  CAS  Google Scholar 

  44. Kaufman HW, Kleinberg I (1971) An x-ray crystallographic examination of calcium phosphate formation in Ca(OH)2/H3PO4 mixtures. Calcif Tissue Res 6:335–342

    Google Scholar 

  45. Füredi-Milhofer H, Oljica-Zabric E, Purgaric B, Kosar-Grasic B, Pavkovic N (1975) Precipitation of calcium phosphates from electrolyte solutions. IV. Precipitation diagrams of the system calcium chloride-sodium phosphate-0.15 M sodium chloride. J Inorg Nucl Chem 37:2047–2051

    Article  Google Scholar 

  46. LeGeros RZ, LeGeros JP (1972) Brushite crystals grown by diffusion in silica gel and in solution. J Cryst Growth 13/14: 476–480

    Article  Google Scholar 

  47. LeGeros RZ, Lee D, Quirologico G, Shirra WP, Reich L (1983)In vitro formation of dicalcium phosphate dihydrate, CaHPO4·2H2O (DCPD). Scan Electron Micr 11:407–418

    Google Scholar 

  48. Elliot JS, Sharp RF, Lewis L (1959) The effect of the molar Ca/P ratio upon the crystallization of brushite and apatite. J Phys Chem 63:725–726

    Article  Google Scholar 

  49. Shapiro IM, Lee NH (1978) The effect of oxygen, phosphoenolpyruvate and pH on the release of calcium from chondrocyte mitochondria. Metab Bone Dis Rel Res 1:173–177

    Article  CAS  Google Scholar 

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Wuthier, R.E., Rice, G.S., Wallace, J.E.B. et al. In vitro precipitation of calcium phosphate under intracellular conditions: formation of brushite from an amorphous precursor in the absence of ATP. Calcif Tissue Int 37, 401–410 (1985). https://doi.org/10.1007/BF02553710

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