Differential effects of tumor necrosis factor and asbestos fibers on manganese superoxide dismutase induction and oxidant-induced cytotoxicity in human mesothelial cells

• Published in: Cell biology and toxicology 1996-06, Vol.12 (3), p.167-175
• Main Authors: PIETARINEN-RUNTTI, P, RAIVIO, K. O, LINNAINMAA, K, EKMAN, A, SAKSELA, M, KINNULA, V. L
• Format: Article
• Language: English
• Subjects: Asbestos, Amosite - toxicity; Biological and medical sciences; Blotting, Northern; Cell Line, Transformed; Cell Survival - drug effects; Chemical and industrial products toxicology. Toxic occupational diseases; Enzyme Induction - drug effects; Epithelium - drug effects; Epithelium - enzymology; Humans; Inorganic dusts (pneumoconiosises) and organic dusts (byssinosis etc.); L-Lactate Dehydrogenase - metabolism; Medical sciences; Oxidation-Reduction; Pleura - drug effects; Pleura - enzymology; RNA, Messenger - metabolism; Superoxide Dismutase - biosynthesis; Toxicology; Tumor Necrosis Factor-alpha - toxicity; Up-Regulation - drug effects
• ISSN: 0742-2091; 1573-6822
• DOI: 10.1007/BF00148170

We compared induction of manganese superoxide dismutase (MnSOD) by asbestos fibers and tumor necrosis factor alpha (TNF) using cultured human mesothelial cells. Transformed pleural mesothelial cells (MET 5A) were exposed for 48 h to amosite asbestos fibers (2 micrograms/cm2), to TNF (10 ng/ml), and to the combination of these two. TNF and amosite+TNF caused significant MnSOD mRNA upregulation. Similarly MnSOD specific activity was increased by TNF (290% increase) and the amosite+TNF combination (313% increase) but not by amosite alone. In cell injury experiments, amosite and amosite+TNF exposures caused significant cell membrane injury when assessed by lactate dehydrogenase release, which was 31% and 57% higher than in the unexposed cells. However, only the amosite+TNF combination caused significant depletion of cellular high-energy nucleotide when expressed as percentage of [14C]adenine labeling in cellular high-energy nucleotides. The nucleotide levels were 91.5 +/- 2.0% in the unexposed cells, 89.9 +/- 3.9% in amosite-exposed cells, 90.1 +/- 2.2% in TNF-exposed cells, and 79.8 +/- 9.4% in amosite+TNF-exposed cells. Amosite+TNF-exposed cells were also most sensitive to menadione (20 mumol/L, 2 h), a compound which generates superoxide radicals intracellularly. In conclusion, our data suggests that in human mesothelial cells inflammatory cytokines but not asbestos fibers alone can cause MnSOD induction. In this study, however amosite asbestos+TNF treatment rendered these cells more vulnerable to oxidant-induced cell damage despite elevated MnSOD activity.