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. 1968 Oct 1;39(1):55–76. doi: 10.1083/jcb.39.1.55

MICROINCINERATION, ELECTRON MICROSCOPY, AND ELECTRON DIFFRACTION OF CALCIUM PHOSPHATE-LOADED MITOCHONDRIA

Richard S Thomas 1, John W Greenawalt 1
PMCID: PMC2107513  PMID: 4878171

Abstract

Isolated rat liver mitochondria were incubated in vitro under conditions supporting the massive accumulation of calcium and phosphate. Samples were embedded, thin sectioned, and examined in the electron microscope. The intramitochondrial distribution of insoluble or structure-bound mineral substances was studied by electron microscopy coupled with recently developed techniques of high resolution microincineration. As shown previously, the ion-loaded mitochondria acquire large, internal granules which have inherent electron opacity indicative of high mineral content. Study of ash patterns in preselected areas of sections directly confirmed the high mineral content of the granules, and the appearance of the residues was consistent with the copresence in the granules of some organic material. Other mitochondrial structures were almost devoid of mineral. Thin sections of unincubated control mitochondria also were incinerated. They were found to contain appreciable amounts of intrinsic mineral, seemingly associated with membranes. The normal, dense matrix granules commonly seen in unaltered mitochondria could be seen in intact sections of these control preparations, but after burning no definite correspondence of any ash to the granules could be demonstrated. The normal granules perhaps do not contain mineral. Heating experiments on ash patterns of all the preparations demonstrated the thermal stability and crystallizability of the ash. The crystallized ash of the in vitro-produced dense granules was tentatively shown by electron diffraction to be β-tricalcium phosphate (whitlockite). This, together with evidence from the literature, suggests that the original, noncrystalline mineral may be a colloidal, subcrystalline precursor of calcium-deficient hydroxyapatite. Experiments were performed on synthetic calcium phosphates for comparison. Other possible applications of the microincineration techniques are briefly discussed.

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Selected References

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  1. BOOTHROYD B. THE PROBLEM OF DEMINERALISATION IN THIN SECTIONS OF FULLY CALCIFIED BONE. J Cell Biol. 1964 Jan;20:165–173. doi: 10.1083/jcb.20.1.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bruni C., Porter K. R. The Fine Structure of the Parenchymal Cell of the Normal Rat Liver: I. General Observations. Am J Pathol. 1965 May;46(5):691–755. [PMC free article] [PubMed] [Google Scholar]
  3. CAULFIELD J. B., SCHRAG P. E. ELECTRON MICROSCOPIC STUDY OF RENAL CALCIFICATION. Am J Pathol. 1964 Mar;44:365–381. [PMC free article] [PubMed] [Google Scholar]
  4. Cameron D. A., Paschall H. A., Robinson R. A. Changes in the fine structure of bone cells after the administration of parathyroid extract. J Cell Biol. 1967 Apr;33(1):1–14. doi: 10.1083/jcb.33.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Eanes E. D., Gillessen I. H., Posner A. S. Intermediate states in the precipitation of hydroxyapatite. Nature. 1965 Oct 23;208(5008):365–367. doi: 10.1038/208365a0. [DOI] [PubMed] [Google Scholar]
  6. Fleischer S., Fleischer B., Stoeckenius W. Fine structure of lipid-depleted mitochondria. J Cell Biol. 1967 Jan;32(1):193–208. doi: 10.1083/jcb.32.1.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GLEIT C. E. Electronic apparatus for ashing biologic specimens. Am J Med Electron. 1963 Apr-Jun;2:112–118. [PubMed] [Google Scholar]
  8. GONZALES F., KARNOVSKY M. J. Electron microscopy of osteoclasts in healing fracturees of rat bone. J Biophys Biochem Cytol. 1961 Feb;9:299–316. doi: 10.1083/jcb.9.2.299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Greenawalt J. W., Carafoli E. Electron microscope studies on the active accumulation of Sr++ by rat-liver mitochondria. J Cell Biol. 1966 Apr;29(1):37–61. doi: 10.1083/jcb.29.1.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HEGGTVEIT H. A., HERMAN L., MISHRA R. K. CARDIAC NECROSIS AND CALCIFICATION IN EXPERIMENTAL MAGNESIUM DEFICIENCY. A LIGHT AND ELECTRON MICROSCOPIC STUDY. Am J Pathol. 1964 Nov;45:757–782. [PMC free article] [PubMed] [Google Scholar]
  11. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. PEACHEY L. D. ELECTRON MICROSCOPIC OBSERVATIONS ON THE ACCUMULATION OF DIVALENT CATIONS IN INTRAMITOCHONDRIAL GRANULES. J Cell Biol. 1964 Jan;20:95–111. doi: 10.1083/jcb.20.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. ROSSI C. S., LEHNINGER A. L. STOICHIOMETRIC RELATIONSHIPS BETWEEN ACCUMULATION OF IONS BY MITOCHONDRIA AND THE ENERGY-COUPLING SITES IN THE RESPIRATORY CHAIN. Biochem Z. 1963;338:698–713. [PubMed] [Google Scholar]
  14. ROSSI C. S., LEHNINGER A. L. Stoichiometric relationships between mitochondrialion accumulation and oxidative phosphorylation. Biochem Biophys Res Commun. 1963 Jun 20;11:441–446. doi: 10.1016/0006-291x(63)90089-5. [DOI] [PubMed] [Google Scholar]
  15. Reynolds E. S. Liver parenchymal cell injury. 3. The nature of calcium--associated electron-opaque masses in rat liver mitochondria following poisoning with carbon tetrachloride. J Cell Biol. 1965 Jun;25(3 Suppl):53–75. doi: 10.1083/jcb.25.3.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. SABATINI D. D., BENSCH K., BARRNETT R. J. Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation. J Cell Biol. 1963 Apr;17:19–58. doi: 10.1083/jcb.17.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. THOMAS R. S. ULTRASTRUCTURAL LOCALIZATION OF MINERAL MATTER IN BACTERIAL SPORES BY MICRONINCINERATION. J Cell Biol. 1964 Oct;23:113–133. doi: 10.1083/jcb.23.1.113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. TRAUTZ O. R. X-ray diffraction of biological and synthetic apatites. Ann N Y Acad Sci. 1955 Apr 27;60(5):696–712. doi: 10.1111/j.1749-6632.1955.tb40060.x. [DOI] [PubMed] [Google Scholar]
  19. Termine J. D., Posner A. S. Infrared analysis of rat bone: age dependency of amorphous and crystalline mineral fractions. Science. 1966 Sep 23;153(3743):1523–1525. doi: 10.1126/science.153.3743.1523. [DOI] [PubMed] [Google Scholar]
  20. VASINGTON F. D., MURPHY J. V. Ca ion uptake by rat kidney mitochondria and its dependence on respiration and phosphorylation. J Biol Chem. 1962 Aug;237:2670–2677. [PubMed] [Google Scholar]
  21. WATSON M. L., ROBINSON R. A. Collagen-crystal relationships in bone. II. Electron microscope study of basic calcium phosphate crystals. Am J Anat. 1953 Jul;93(1):25–59. doi: 10.1002/aja.1000930103. [DOI] [PubMed] [Google Scholar]
  22. WEISS J. M. Mitochondrial changes induced by potassium and sodium in the duodenal absorptive cell as studied with the electron microscope. J Exp Med. 1955 Dec 1;102(6):783–788. doi: 10.1084/jem.102.6.783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Weinbach E. C., Von Brand T. Formation, isolation and composition of dense granules from mitochondria. Biochim Biophys Acta. 1967 Oct 9;148(1):256–266. doi: 10.1016/0304-4165(67)90301-7. [DOI] [PubMed] [Google Scholar]
  24. Wlodawer P., Parsons D. F., Williams G. R., Wojtczak L. Morphological changes in isolated rat-liver mitochondria during swelling and contraction. Biochim Biophys Acta. 1966 Oct 17;128(1):34–47. doi: 10.1016/0926-6593(66)90139-1. [DOI] [PubMed] [Google Scholar]

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