Literature DB >> 3744904

Effects of ethidium bromide, tetramethylethidium bromide and betaine B on the ultrastructure of HeLa cell mitochondria in situ. A comparative binding study.

J Röding, A Naujok, H W Zimmermann.   

Abstract

Several investigators have described the ultrastructural changes that occur in the mitochondria of cells in tissue cultures after treatment with the drug ethidium bromide (E). The mitochondria swell and the cristae become greatly altered and finally disappear; in the cristae-free region of the matrix electron-dense granules can be observed. It has been assumed that intercalation of E between the base pairs of the mitochondrial DNA induces the formation of the granular inclusions. To investigate whether intercalation is really the initial step in the generation of dense granules inside the matrix, we performed a comparative incubation study of HeLa-cell mitochondria in situ using three closely related dyes (D), i.e., E, tetramethylethidium bromide (TME) and betaine B (B). They strongly differ with regard to their affinity for DNA and their ability to cross membranes. E was used as a reference dye. TME does not intercalate, but is externally bound to DNA only weakly. The neutral B is not bound at all, but can cross membranes more easily than the cation E. Moreover, in aqueous solutions at pH approximately equal to 7.0, B is in equilibrium with its protonated cation BH. BH and E have almost equal affinities for DNA. Therefore B may quickly pass the inner mitochondrial membranes and the cristae, and should then be bound inside the matrix, thus forming a BH-DNA complex. On the assumption that intercalation is necessary for the generation of intramitochondrial electron-dense bodies, we predicted that BH/B should be more efficient than E, while TME should be relatively ineffective.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3744904     DOI: 10.1007/bf00494807

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  13 in total

1.  Ultrastructure and microchemical composition of ethidium bromide-induced intramitochondrial complexes.

Authors:  M McGill; P S Baur; T C Hsu
Journal:  Exp Cell Res       Date:  1976-04       Impact factor: 3.905

2.  [Hydrophobic acridine dyes for fluorescent staining of mitochondria in living cells. 3. Specific accumulation of the fluorescent dye NAO on the mitochondrial membranes in HeLa cells by hydrophobic interaction. Depression of respiratory activity, changes in the ultrastructure of mitochondria due to NAO. Increase of fluorescence in vital stained mitochondria in situ by irradiation].

Authors:  M Septinus; T Berthold; A Naujok; H W Zimmermann
Journal:  Histochemistry       Date:  1985

3.  Fixation and embedment, in situ, of tissue culture cells for electron microscopy.

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Review 4.  Mitochondrial form and function relationships in vivo: their potential in toxicology and pathology.

Authors:  R A Smith; M J Ord
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5.  Procedure for embedding in situ selected cells cultured in vitro.

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Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

6.  INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS. II. ENZYMATIC AND OTHER HYDROLYTIC TREATMENTS.

Authors:  S NASS; M M NASS
Journal:  J Cell Biol       Date:  1963-12       Impact factor: 10.539

7.  The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.

Authors:  E S REYNOLDS
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

8.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

9.  Electron-dense structures in mitochondria induced by short-term ethidium bromide treatment.

Authors:  M McGill; T C Hsu; B R Brinkley
Journal:  J Cell Biol       Date:  1973-10       Impact factor: 10.539

10.  Effects of ethidium bromide on the cytochrome content and ultrastructure of L cell mitochondria.

Authors:  G Soslau; M M Nass
Journal:  J Cell Biol       Date:  1971-11       Impact factor: 10.539

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  5 in total

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Journal:  Histochemistry       Date:  1990

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Authors:  R W Horobin; F Rashid
Journal:  Histochemistry       Date:  1990

Review 3.  Hydroethidine- and MitoSOX-derived red fluorescence is not a reliable indicator of intracellular superoxide formation: another inconvenient truth.

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4.  Photoaffinity labelling with fluorescence detection. Dye accumulation at four mitochondrial proteins in HeLa and LM cells.

Authors:  K Schneider; H W Zimmermann
Journal:  Histochemistry       Date:  1994-02

5.  A lipophilic cation protects crops against fungal pathogens by multiple modes of action.

Authors:  Gero Steinberg; Martin Schuster; Sarah J Gurr; Tina A Schrader; Michael Schrader; Mark Wood; Andy Early; Sreedhar Kilaru
Journal:  Nat Commun       Date:  2020-03-30       Impact factor: 14.919

  5 in total

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