Literature DB >> 3967286

Characterization of an oxygen-tolerant cell line derived from Chinese hamster ovary. Antioxygenic enzyme levels and ultrastructural morphometry of peroxisomes and mitochondria.

P van der Valk, J J Gille, A B Oostra, E W Roubos, T Sminia, H Joenje.   

Abstract

To study the cellular defense mechanism against oxygen toxicity, an oxygen-tolerant cell line from Chinese hamster ovary (CHO) was obtained by multistep adaptation to increased O2 levels. The hyperoxia-adapted (HA) cells were able to proliferate under an atmosphere of 99% O2/1% CO2, an O2 tension lethal to the parental (control) cells. When grown under normoxic conditions (20% O2/1% CO2/79% N2) the cells remained tolerant for at least 8 weeks, suggesting a genetic basis for the oxygen tolerance. Compared to the parental cells, the HA cells were irregularly shaped, had larger mitochondria, contained more lipid droplets and showed a reduced growth rate. Ultrastructural morphometry revealed a 1.8-fold (p less than 0.001) increase of the mitochondrial volume fraction in the HA cells, resulting from an increase in both number and average volume of the mitochondria. The volume fraction of peroxisomes was increased over two-fold in the HA cells, as appeared from a approximately 1.9-fold (p less than 0.001) increase in number and a 1.2-fold (p less than 0.025) increase in size. There was no evidence for ultrastructural damage in the HA cells. Specific activities of antioxygenic enzymes were considerably higher in the HA cells compared to controls: CuZn-superoxide dismutase, X 2.5; Mn-superoxide dismutase, X 2.1; catalase, X 4.0; glutathione peroxidase, X 1.9. Oxygen tolerance in CHO cells is therefore associated with increased levels of antioxygenic enzymes, confirming the proposed important role of these enzymes in the defense against oxygen toxicity.

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Year:  1985        PMID: 3967286     DOI: 10.1007/bf00214903

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  40 in total

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Authors:  T Hashimoto
Journal:  Ann N Y Acad Sci       Date:  1982       Impact factor: 5.691

3.  Liposome-mediated augmentation of superoxide dismutase in endothelial cells prevents oxygen injury.

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Review 4.  Oxygen toxicity of the lung: an update.

Authors:  S M Deneke; B L Fanburg
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5.  An improved coupled test procedure for glutathione peroxidase (EC 1-11-1-9-) in blood.

Authors:  W A Günzler; H Kremers; L Flohé
Journal:  Z Klin Chem Klin Biochem       Date:  1974-10

6.  Atmospheric stability in cell culture vessels.

Authors:  A K Balin; D B Goodman; H Rasmussen; V J Cristofalo
Journal:  In Vitro       Date:  1976-10

7.  Studies of hepatic mitochondrial structure and function: morphometric and biochemical evaluation of in vivo perturbation by arsenate.

Authors:  B A Fowler; J S Woods; C M Schiller
Journal:  Lab Invest       Date:  1979-10       Impact factor: 5.662

8.  Copper- and zinc-containing superoxide dismutase, manganese-containing superoxide dismutase, catalase, and glutathione peroxidase in normal and neoplastic human cell lines and normal human tissues.

Authors:  S L Marklund; N G Westman; E Lundgren; G Roos
Journal:  Cancer Res       Date:  1982-05       Impact factor: 12.701

9.  Oxygen: our major carcinogen?

Authors:  H Joenje
Journal:  Med Hypotheses       Date:  1983-09       Impact factor: 1.538

10.  Relationship between morphological changes and lipid-lowering action of p-chlorphenoxyisobutyric acid (CPIB) on hepatic mitochondria and peroxisomes in man.

Authors:  M Hanefeld; C Kemmer; E Kadner
Journal:  Atherosclerosis       Date:  1983-02       Impact factor: 5.162

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  8 in total

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3.  In vitro modulation of antioxidant enzymes in normal and malignant renal epithelium.

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7.  Peroxisomal biogenesis in ischemic brain.

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Journal:  Antioxid Redox Signal       Date:  2015-01-10       Impact factor: 8.401

Review 8.  Control of mitochondrial dynamics and apoptotic pathways by peroxisomes.

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  8 in total

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