Abstract
Rat liver mitochondria allowed to accumulate maximal amounts of Ca++ and HPO4 = ions from the suspending medium in vitro during respiration have a considerably higher specific gravity than normal mitochondria and may be easily separated from the latter by isopycnic centrifugation in density gradients of sucrose or cesium chloride. When the mitochondria are allowed to accumulate less than maximal amounts of Ca++ and HPO4 = from the medium, they have intermediate specific gravities which are roughly proportional to their content of calcium phosphate. Maximally "loaded" mitochondria are relatively homogeneous with respect to specific gravity. Correlated biochemical and electron microscopic studies show that Ca++-loaded mitochondria contain numerous dense granules, of which some 85 per cent are over 500 A in diameter. These granules are electron-opaque not only following fixation and staining with heavy metal reagents, but also following fixation with formaldehyde, demonstrating that the characteristic granules in Ca++-loaded mitochondria have intrinsic electron-opacity. The dense granules are almost always located within the inner compartment of the mitochondria and not in the space between the inner and outer membranes. They are frequently located at or near the cristae and they often show electron-transparent "cores." Such granules appear to be made up of clusters of smaller dense particles, but preliminary x-ray diffraction analysis and electron diffraction studies have revealed no evidence of crystallinity in the deposits. The electron-opaque granules decrease in number when the Ca++-loaded mitochondria are incubated with 2,4-dinitrophenol; simultaneously there is discharge of Ca++ and phosphate from the mitochondria into the medium.
Full Text
The Full Text of this article is available as a PDF (1.7 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BRIERLEY G. P., BACHMANN E., GREEN D. E. Active transport of inorganic phosphate and magnesium ions by beef heart mitochondria. Proc Natl Acad Sci U S A. 1962 Nov 15;48:1928–1935. doi: 10.1073/pnas.48.11.1928. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BRIERLEY G. P., MURER E., GREEN D. E. Participation of an intermediate of oxidative phosphorylation in ion accumulation by mitochondria. Science. 1963 Apr 5;140(3562):60–62. doi: 10.1126/science.140.3562.60. [DOI] [PubMed] [Google Scholar]
- BRIERLEY G., MURER E., BACHMANN E., GREEN D. E. STUDIES ON ION TRANSPORT. II. THE ACCUMULATION OF INORGANIC PHOSPHATE AND MAGNESIUM IONS BY HEART MITOCHONDRIA. J Biol Chem. 1963 Oct;238:3482–3489. [PubMed] [Google Scholar]
- DELUCA H. F., ENGSTROM G. W. Calcium uptake by rat kidney mitochondria. Proc Natl Acad Sci U S A. 1961 Nov 15;47:1744–1750. doi: 10.1073/pnas.47.11.1744. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FOLCH J., LEES M., SLOANE STANLEY G. H. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957 May;226(1):497–509. [PubMed] [Google Scholar]
- 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]
- KARNOVSKY M. J. Simple methods for "staining with lead" at high pH in electron microscopy. J Biophys Biochem Cytol. 1961 Dec;11:729–732. doi: 10.1083/jcb.11.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- NEUBERT D., FOSTER G. V., LEHNINGER A. L. Effect of temperature on uptake and extrusion of water by isolated rat-liver mitochondria. Biochim Biophys Acta. 1962 Jul 16;60:492–498. doi: 10.1016/0006-3002(62)90868-5. [DOI] [PubMed] [Google Scholar]
- 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]
- REYNOLDS E. S., THIERS R. E., VALLEE B. L. Mitochondrial function and metal content in carbon tetrachloride poisoning. J Biol Chem. 1962 Nov;237:3546–3551. [PubMed] [Google Scholar]
- 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]
- SCOTT D. B., NYLEN M. U., VON BRAND T., PUGH M. H. The mineralogical composition of the calcareous corpuscles of Taenia taeniaeformis. Exp Parasitol. 1962 Dec;12:445–458. doi: 10.1016/0014-4894(62)90081-4. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]