この研究は、細胞傷害性Tリンパ球(CTLL-2)におけるインターロイキン2(IL-2)依存性の増殖に対する無線周波(RF:2450MHz)電磁界ばく露の影響の有無を調べた。様々な生理学的濃度のIL-2 細胞の存在下(あるいは存在なし)で培養したCTLL-2にRFばく露を行い、ばく露終了の直後および24時間後の三重水素チミジン取り込み測定により増殖への影響を調べた。その結果、SARが25W/kg(誘導電界強度98.4V/m)以上で、特にIL-2が低濃度の場合、CTLL-2の増殖が有意に低下した;それより低いSARでは、ばく露直後の増殖は上昇したが、24時間後では低下した、と報告している。
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To study the effects of radiofrequency irradiation on interleukin-2-dependent proliferation of cytolytic T lymphocytes (CTLL-2).
After antigenic activation CTLL-2 express high-affinity receptors for the hormone interleukin-2. Binding of interleukin-2 is necessary and sufficient for T cell proliferation. After exposure to radiofrequency cells were cultured at various physiological concentrations of interleukin-2 (0, 0.62, 1.25, 2.5, 5, 10, 20, or 40 U/ml).
CTLL-2 cells were also incubated for 2 h at 37, 38, 39, 40, or 41°C without electromagnetic field exposure (temperature control).
ばく露 | パラメータ |
---|---|
ばく露1:
2.45 GHz
Modulation type:
CW
ばく露時間:
continuous for 2 h
|
|
ばく露2:
2.45 GHz
Modulation type:
pulsed
ばく露時間:
continuous for 2 h
|
周波数 | 2.45 GHz |
---|---|
タイプ |
|
ばく露時間 | continuous for 2 h |
Modulation type | CW |
---|
ばく露の発生源/構造 | |
---|---|
ばく露装置の詳細 | Cells were simultaneously RF and sham exposed in identical waveguide exposure chambers maintaining isothermal conditions at 37 ± 0.1°C as described previously [Liu et al., 1988]. |
Sham exposure | A sham exposure was conducted. |
Additional information | Thermal control cultures were incubated for 2 h at 37, 38, 39, 40, or 41°C in the chambers used for MW exposure. |
周波数 | 2.45 GHz |
---|---|
タイプ |
|
ばく露時間 | continuous for 2 h |
Modulation type | pulsed |
---|---|
Pulse width | 6.67 ms |
Repetition frequency | 50 Hz |
Additional information |
simulating PCS modulation |
ばく露の発生源/構造 |
|
---|---|
Sham exposure | A sham exposure was conducted. |
Exposure to 2450 MHz radiofrequency irradiation at specific absorption rates of greater than 25 W/kg induced a consistent, statistically significant reduction in CTLL-2 proliferation, especially at low interleukin-2 concentrations. At lower specific absorption rates, exposure increased CTLL-2 proliferation immediately after exposure but reduced 24 h postexposure proliferation.
Radiofrequency irradiation effects depended on the mitotic state of the cells at the time of exposure. Comparison of the effects of temperature elevation (temperature control) and radiofrequency irradiation indicated significant qualitative and quantitative differences.
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