{"title":"Effect of ethanol on natural killer cell activity in vitro.","authors":"S F Luo, C T Liu","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effect of ethanol on kinetic stages of natural killer (NK) cell activity was studied in vitro. Peripheral blood mononuclear cells (MNC) were either co-cultured or pre-incubated with various ethanol concentrations and assayed for NK cell activity with a \"4-hour chromium release assay\" and a \"single cell cytotoxicity assay in agarose\" simultaneously. Direct addition of ethanol to the assay system resulted in a dose-dependent inhibition of NK cell activity. The percentage of lysed conjugated target cells was suppressed from a control value of 21.2% to 17.0%, 15.1%, 11.8% and 10.0% with an ethanol concentration of 0.125%, 0.25%, 0.5% and 1.0%, respectively. NK cell recycling was also inhibited. A 24-hour pre-incubation with ethanol, however, resulted in NK cell activity enhancement. The enhancement was around 20% with a 0.25% ethanol concentration and around 45% with a 0.5% and a 1.0% ethanol concentrations. The enhancing effect was noted mainly at the cytolysis stage after binding of effector cell with target cells.</p>","PeriodicalId":22189,"journal":{"name":"Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association","volume":"88 9","pages":"863-8"},"PeriodicalIF":0.0000,"publicationDate":"1989-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The effect of ethanol on kinetic stages of natural killer (NK) cell activity was studied in vitro. Peripheral blood mononuclear cells (MNC) were either co-cultured or pre-incubated with various ethanol concentrations and assayed for NK cell activity with a "4-hour chromium release assay" and a "single cell cytotoxicity assay in agarose" simultaneously. Direct addition of ethanol to the assay system resulted in a dose-dependent inhibition of NK cell activity. The percentage of lysed conjugated target cells was suppressed from a control value of 21.2% to 17.0%, 15.1%, 11.8% and 10.0% with an ethanol concentration of 0.125%, 0.25%, 0.5% and 1.0%, respectively. NK cell recycling was also inhibited. A 24-hour pre-incubation with ethanol, however, resulted in NK cell activity enhancement. The enhancement was around 20% with a 0.25% ethanol concentration and around 45% with a 0.5% and a 1.0% ethanol concentrations. The enhancing effect was noted mainly at the cytolysis stage after binding of effector cell with target cells.