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L929 murine lung epithelial cells, as well as human IMR-90 and XP-12BE cells, were exposed to 2450 MHz MW at 0.013, 0.026, 0.039, 0.13, and 1.3 W/kg for 4 hours. Exposure resulted in no changes in cell viability or proliferation rate in any cell type. In addition, exposure of L929 cells at 0.13 W/kg (as above) was performed followed by incubation for 18 hours and the activity of interferon regulated 2'-5' oligoadenylate synthetase (2-5 A) and 2'-5' oligoadenylate ribonuclease (RNase L) was analyzed. The authors reported no effect of non-thermal MW exposure on cell viability or proliferation rate. Further, the lack of a negative effect on XP cells, deficient in DNA damage repair, makes a direct damage to the DNA unlikely. In cells exposed as above followed by incubation for 18 hours, however, the activity of 2'-5' oligoadenylate ribonuclease (RNase L) binding to 2'-5' A and subsequent RNase activity was increased, although no change was reported in the activity of interferon regulated 2’-5’ oligoadenylate synthetase (2-5 A) The authors conclude that, although exposure did not affect cell viability, direct DNA damage, or proliferation rate, it may have effects on certain enzyme activity. |
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There was no positive control for the enzyme activity measurements. There was also no temperature monitoring during exposure. Sham exposure alone resulted in a ~14% increase in 2’-5’ A binding and RNase L activity indicating that some of the effects might have been induced by the manipulation of the cells during exposure, trypsinization, or re-plating steps. Further, enzyme activity should have also been assayed following exposure at the higher dose level (1.3 W/kg – used for cell viability and proliferation assays in the same paper) to achieve a potential dose response to better verify and characterize the finding. |