Acetaldehyde exposure causes growth inhibition in a Chinese hamster ovary cell line that expresses alcohol dehydrogenase
| Autor: | Barbara T. Zimmerman, John E. Mapoles, Mieko Iwahashi, Danièle Lucas, F. R. Simon |
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| Rok vydání: | 1994 |
| Předmět: |
Ethanol
biology Dose-Response Relationship Drug Cell Survival Chinese hamster ovary cell Acetaldehyde Alcohol Dehydrogenase Medicine (miscellaneous) ADH1B CHO Cells Toxicology Gene Expression Regulation Enzymologic Psychiatry and Mental health chemistry.chemical_compound chemistry Biochemistry Cell culture Cricetinae biology.protein Animals Allyl alcohol Ethanol metabolism Cell Division Alcohol dehydrogenase |
| Zdroj: | Alcoholism, clinical and experimental research. 18(3) |
| ISSN: | 0145-6008 |
| Popis: | Chronic ethanol exposure causes many pathophysiological changes in cellular function due to ethanol itself and/or the effects of its metabolism (i.e., generation of acetaldehyde and redox equivalents). However, the role of each of these effects remains controversial. To address these questions, we have developed a cell line that expresses alcohol dehydrogenase. This cell line permits separate examination of the effects of ethanol and its metabolite acetaldehyde on cell function. An expression vector for the mouse liver alcohol dehydrogenase was constructed and transfected into Chinese hamster ovary cells. Cells expressing alcohol dehydrogenase were identified by screening with allyl alcohol, which is metabolized by alcohol dehydrogenase to the toxic aldehyde acrolein. A number of cell lines were identified that expressed alcohol dehydrogenase. A-10 cells were selected for further study because of their high sensitivity to allyl alcohol, suggesting a high level of alcohol dehydrogenase expression. These cells expressed a mRNA that hybridizes with the alcohol dehydrogenase cDNA and had an alcohol dehydrogenase activity comparable to murine liver. When cultures of these cells were exposed to ethanol, acetaldehyde was detected in both the medium and cells. The acetaldehyde concentration in the medium remained constant for at least 1 week in culture and was a function of the added ethanol concentration. Chronic exposure of A-10 cells to ethanol resulted in a dose-dependent reduction in the number of cells that accumulated over 7 days. Ethanol-treated cells remained viable, and growth inhibition was reversible. Growth inhibition was blocked by the alcohol dehydrogenase inhibitor 4-methylpyrazole, suggesting that acetaldehyde and not ethanol was responsible for growth inhibition in these cells. |
| Databáze: | OpenAIRE |
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