This study describes the isolation and subsequent characterization of four mammalian cell lines resistant to ethidium bromide (EB). Treatment of the simian virus 40- (SV40) transformed hamster cell line F5-1 first led to the establishment of the F2 cell line, which is resistant to 2 µg EB/ml. At this concentration cytochromes c and b are present in almost normal or only slightly diminished amounts, whereas cytochromes a + a3 show an obvious decrease. The mitochondria of the F2 cell show a normal ultrastructure, not distinct from the parental cell line F5-1, and contain closed circular DNA. The sensitive parental F5-1 cells, however, when exposed to the same dye concentration exhibit the typical EB-induced ultrastructural changes in the mitochondria, and no more component I mitochondrial DNA can be demonstrated. 1 yr after establishment we derived from the F2 cell three more cell lines, resistant against 4, 8, and 16 µg of EB/ml. These cell lines, termed F4, F8, and F16, respectively, also revealed relatively intact-appearing mitochondria, although distinguishable from F5-1 and F2 mitochondria by a more condensed or unorthodox cristae conformation. F4, F8, and F16 cell lines contained closed circular mitochondrial DNA in the same position as that of the parental F5-1 cells, when analyzed in an isopycnic CsCl-EB gradient. A small shoulder at the lower density side of the DNA I peaks was observed. The newly acquired drug resistance of the F cells is hereditarily transmitted to the progeny cells and retained even after a period of growth in EB-free medium.
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1 July 1973
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July 01 1973
ESTABLISHMENT AND CHARACTERIZATION OF ETHIDIUM BROMIDE RESISTANCE IN SIMIAN VIRUS 40-TRANSFORMED HAMSTER CELLS : Effects on Mitochondria In Vivo
Wolfgang Klietmann,
Wolfgang Klietmann
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
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Nobuhiro Sato,
Nobuhiro Sato
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
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Margit M. K. Nass
Margit M. K. Nass
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
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Wolfgang Klietmann
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
Nobuhiro Sato
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
Margit M. K. Nass
From the Abteilung Medizinische Mikrobiologie der Medizinischen Fakultät der Rheinisch-West-fälischen Technischen Hochschule, 51 Aachen, Germany, the Department of Biophysics, Johnson Research Foundation, University of Pennsylvania, and the Department of Therapeutic Research, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104.
Dr. Sato's pres-present address is the Department of Biochemistry, School of Medicine, Osaka University, Osaka, Japan.
Received:
September 29 1972
Revision Received:
March 12 1973
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1973 by The Rockefeller University Press
1973
J Cell Biol (1973) 58 (1): 11–26.
Article history
Received:
September 29 1972
Revision Received:
March 12 1973
Citation
Wolfgang Klietmann, Nobuhiro Sato, Margit M. K. Nass; ESTABLISHMENT AND CHARACTERIZATION OF ETHIDIUM BROMIDE RESISTANCE IN SIMIAN VIRUS 40-TRANSFORMED HAMSTER CELLS : Effects on Mitochondria In Vivo . J Cell Biol 1 July 1973; 58 (1): 11–26. doi: https://doi.org/10.1083/jcb.58.1.11
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