Abstract
In view of the unsatisfactory appearance, under the electron microscope, of liver mitochondria isolated in isotonic sucrose medium, alternative media have been examined. It was found to be advantageous to replace sucrose by raffinose, and to add levan or, preferably, dextran, together with heparin in suitable concentration. With the optimal medium, the constituents of which are raffinose, versene (optional), dextran of high molecular weight, heparin, and AMP (optional), most of the mitochondria in the osmium-fixed pellet are apparently intact, and show the membranes characteristic of mitochondria as seen in cell sections. The optimal medium has no adverse effect on the activity of the several tissue enzymes which have been studied, except that Mg++-activated ATPase is partially inhibited if the medium is present in high concentration in the assay system. Mitochondrial fractions isolated in the new medium have, in common with sucrose fractions, appreciable "free" ATPase activity, this activity being evidently a poor criterion of mitochondrial integrity. Use of the new medium does not decrease the proportion of cytoplasmic ATPase which fails to sediment with the mitochondria, but does give a mitochondrial fraction low in RNA and in acid phosphatase activity and little contaminated with microsomal material. Particles tentatively identified as "lysosomes" have been seen in certain sections.
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- ALBERT S., JOHNSON R. M. The relative amounts of cytoplasmic particles and supernatant and of phosphorus compounds in liver and liver tumors. Cancer Res. 1954 May;14(4):271–276. [PubMed] [Google Scholar]
- BERTHET J., DE DUVE C. Tissue fractionation studies. I. The existence of a mitochondria-linked, enzymically inactive form of acid phosphatase in rat-liver tissue. Biochem J. 1951 Dec;50(2):174–181. doi: 10.1042/bj0500174. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BIRBECK M. S., REID E. A new medium for the isolation of liver mitochondria. Biochim Biophys Acta. 1956 May;20(2):419–421. doi: 10.1016/0006-3002(56)90321-3. [DOI] [PubMed] [Google Scholar]
- CHAUVEAU J., GAUTIER A., MOULE Y., ROUILLER C. Etude morphologique et biochimique de la fraction microsomes des cellules du foie et du pancréas de rat. C R Hebd Seances Acad Sci. 1955 Jul 18;241(3):337–339. [PubMed] [Google Scholar]
- DE DUVE C., PRESSMAN B. C., GIANETTO R., WATTIAUX R., APPELMANS F. Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue. Biochem J. 1955 Aug;60(4):604–617. doi: 10.1042/bj0600604. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DE LAMIRANDE G., ALLARD C., DA COSTA H. C., CANTERO A. Intracellular distribution of acid and alkaline ribonuclease in normal rat liver. Science. 1954 Mar 12;119(3089):351–353. doi: 10.1126/science.119.3089.351. [DOI] [PubMed] [Google Scholar]
- DEMERS M., D'IORIO A., ROBILLARD E. Distribution de l'ATPase dans les diverses populations de mitochondries du foie. Rev Can Biol. 1955 Mar;14(1):89–94. [PubMed] [Google Scholar]
- FAWCETT D. W. Observations on the cytology and electron microscopy of hepatic cells. J Natl Cancer Inst. 1955 Apr;15(5 Suppl):1475–1503. [PubMed] [Google Scholar]
- HOSTER M. S., McBEE B. J., ROLNICK H. A., VAN WINKLE Q., HOSTER H. A. Macromolecular particles obtained from human neoplastic and non-neoplastic lymph nodes. Cancer Res. 1950 Sep;10(9):530–538. [PubMed] [Google Scholar]
- HURLBERT R. B., SCHMITZ H., BRUMM A. F., POTTER V. R. Nucleotide metabolism. II. Chromatographic separation of acid-soluble nucleotides. J Biol Chem. 1954 Jul;209(1):23–39. [PubMed] [Google Scholar]
- KIELLEY W. W., KIELLEY R. K. Myokinase and adenosinetriphosphatase in oxidative phosphorylation. J Biol Chem. 1951 Aug;191(2):485–500. [PubMed] [Google Scholar]
- LARDY H. A., WELLMAN H. The catalytic effect of 2,4-dinitrophenol on adenosinetriphosphate hydrolysis by cell particles and soluble enzymes. J Biol Chem. 1953 Mar;201(1):357–370. [PubMed] [Google Scholar]
- LEWIN I., O'NEAL M. A., REID E. Hormones and liver cytoplasm. 2. Adenosine triphosphatase, glucose 6-phosphatase and xanthine oxidase as affected by hypophysectomy, growth-hormone treatment and adrenalectomy. Biochem J. 1956 Dec;64(4):730–734. doi: 10.1042/bj0640730. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LITTLEFIELD J. W., KELLER E. B., GROSS J., ZAMECNIK P. C. Studies on cytoplasmic ribonucleoprotein particles from the liver of the rat. J Biol Chem. 1955 Nov;217(1):111–123. [PubMed] [Google Scholar]
- MACFARLANE M. G., SPENCER A. G. Changes in the water, sodium and potassium content of rat-liver mitochondria during metabolism. Biochem J. 1953 Jul;54(4):569–575. doi: 10.1042/bj0540569. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALADE G. E. A study of fixation for electron microscopy. J Exp Med. 1952 Mar;95(3):285–298. doi: 10.1084/jem.95.3.285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALADE G. E., PORTER K. R. Studies on the endoplasmic reticulum. I. Its identification in cells in situ. J Exp Med. 1954 Dec 1;100(6):641–656. doi: 10.1084/jem.100.6.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALADE G. E., SIEKEVITZ P. Liver microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Mar 25;2(2):171–200. doi: 10.1083/jcb.2.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SCHNEIDER W. C., HOGEBOOM G. H. Cytochemical studies of mammalian tissues; the isolation of cell components by differential centrifugation: a review. Cancer Res. 1951 Jan;11(1):1–22. [PubMed] [Google Scholar]
- SCHNEIDER W. C., HOGEBOOM G. H., ROSS H. E. Intracellular distribution of enzymes. VII. The distribution of nucleic acids and adenosinetriphosphatase in normal mouse liver and mouse hepatoma. J Natl Cancer Inst. 1950 Feb;10(4):977–982. [PubMed] [Google Scholar]
- SLATER E. C., CLELAND K. W. Stabilization of oxidative phosphorylation in heart-muscle sarcosomes. Nature. 1952 Jul 19;170(4316):118–119. doi: 10.1038/170118b0. [DOI] [PubMed] [Google Scholar]