【目的】無線技術において次第に利用が進んできたミリ波(MMW)放射に対する皮膚細胞の潜在的反応を調べること。【方法】平均入射電力密度1.8mW/cm2、平均の比吸収率42.4 W/kg の60.4 GHz に、ヒトの皮膚の初代培養細胞を1、6、24時間ばく露した。これらのばく露が遺伝子発現に影響するか否かを明らかにするために大規模分析を実施した。41000個のユニークなヒトの転写物プローブセットを入れた遺伝子発現マイクロアレイを用い、真のばく露と擬似ばく露について得られたデータを比較した。【結果】遺伝子発現値についてBenjamini-Hochberg法のような厳密な統計的分析を行った場合、遺伝子発現における有意な差異は観察されなかった。しかし、マイクロアレイデータの分析にt検定を採用した場合、130個の転写物がばく露後に変化した可能性が見出された。定量的に分析するために、これらの転写物から変化の倍率が高く、かつP値が低いというベストな組み合わせをもつ24個の遺伝子を予め選択して、実時間PCRを実施した。これの内の5個(CRIP2、PLXND1、PTX3、SERPINF1、TRPV2)は6時間ばく露後に他とは違う発現をしたことが確認された。【結論】我々が知る限り、これはMMW放射に関連した遺伝子発現変化の可能性を報告した初めての大規模研究である。
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To study the potential responses of skin cells to millimeter wave exposure.
Four independent replicates per condition were used.
ばく露 | パラメータ |
---|---|
ばく露1:
60.4 GHz
Modulation type:
CW
ばく露時間:
continuous for 1, 6, 24 h
|
|
周波数 | 60.4 GHz |
---|---|
タイプ |
|
特性 |
|
ばく露時間 | continuous for 1, 6, 24 h |
Modulation type | CW |
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ばく露の発生源/構造 | |
---|---|
Distance between exposed object and exposure source | 27 cm |
ばく露装置の詳細 | 8.5 cm x 12.7 cm culture plate (six wells) with 0.01 mm cell monolayers in each well placed in an incubator and irradiated from the bottom by a pyramidal horn antenna; horn antenna with an aperture of 22.2 mm x 16.7 mm and 17 dB gain |
Sham exposure | A sham exposure was conducted. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
電力 | 425 mW | - | - | - | antenna output power |
SAR | 39 W/kg | minimum | 計算値 | - | within the outer wells |
SAR | 49.3 W/kg | maximum | 計算値 | - | within the inner wells |
SAR | 42.4 W/kg | spatial average | 計算値 | - | averaged over all six wells |
電力密度 | 1.7 mW/cm² | - | - | - | in the outer wells |
電力密度 | 2.1 mW/cm² | - | - | - | in the inner wells |
電力密度 | 2.3 mW/cm² | peak | - | - | - |
電力密度 | 1.8 mW/cm² | spatial average | - | - | averaged over all six wells |
No significant difference in gene expression was observed when gene expression values were subjected to a stringent statistical analysis (via t-test with a statistical correction). However, when a single t-test (less stringent) was applied, 130 transcripts were found to be potentially modulated after exposure. To further quantitatively analyze these preselected transcripts, real-time RT-PCR was performed on 24 genes with the best combination of high "fold change" and low P-value. Five of them were confirmed as differentially expressed after 6 h of exposure: CRIP2 (a zinc-binding protein involved in signaling, haematopoiesis, and cell proliferation), PLXND1 (a transmembrane receptor involved in development), PTX3 (a protein involved in innate immunity and inflammatory response), SERPINF1 (a secreted endopeptidase inhibitor that has anti-angiogenic and anti-proliferation functions), and TRPV2 (a calcium channel involved in sensory perception).
Compared to other microarray analyses studying the effect of pollutants or drug treatments, the number of responsive genes in the present study is extremely modest. Moreover, the gene expression modification is transient (mostly after 6 h of exposure) and with a limited amplitude (generally with a fold change close to 2). One can only wonder about the consequence on human health, of such subtle changes at cellular level. Thus, the authors conclude that millimeter waves (CW, 60.4 GHz, 1.8 mW/cm²) do not have any dramatic impact on primary cultures of human keratinocytes. However, they cannot exclude that millimeter waves could affect gene expression in vivo because skin is a complex tissue composed of different kinds of cells with various sensitivities.
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