この研究は、マイクロ波ばく露を受けたラットのセルトリ細胞におけるサイトカイン産生を評価し、さらに、マイクロ波ばく露を受けたセルトリ細胞と生殖細胞の共培養が生殖細胞のアポトーシスおよび酸化ストレスに及ぼす影響を調べた。特にTNFalpha、IL-1beta、IL-6が生殖細胞にどのように影響するかに着目した。その結果、マイクロ波ばく露を受けたセルトリ細胞では、TNFalpha、IL-1betaおよびIL-6の増加が示された；これら増加したサイトカインは、生殖細胞の膜にアポトーシスと脂質過酸化を誘発する可能性がある；さらに、生殖細胞のアポトーシスは、Bax / Bcl-2およびカスパーゼ-3の発現増加に関連していた、と報告している。
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To examine the synthesis of cytokines in microwave exposed Sertoli cells of rats and to investigate the effect of a co-incubation of microwave exposed Sertoli cells with germ cells on apoptosis and oxidative stress in germ cells.
Spermatogenesis is the process of male germ cell development from the primordial germ cells to the mature sperm cell. This process can be disturbed by several factors. In this study, molecular mechanisms potentially influencing the spermatogenesis should be examined.
Sertoli cells were isolated from 3-week-old male rats and exposed to microwaves or sham exposed. Afterwards, the synthesis of cytokines was determined. Additionally, the exposed/sham exposed Sertoli cells were re-suspended with trypsin and co-incubated with germ cells (isolated from 8-week-old male rats) in a cell culture. After 24 hours of incubation, the germ cells were collected for further analysis (apoptosis, oxidative stress).
ばく露時間: continuous for up to 24 hours
S Band microwaves
|continuous for up to 24 hours
|S Band microwaves
|A sham exposure was conducted.
Sertoli cells: The gene expression of the tumor necrosis factor-alpha was significantly increased after 2 hours of exposure compared to the sham exposure, while the gene expression of interleukin-1beta and interleukin-6 was significantly increased after 2 and 6 hours of exposure. In the culture medium, the levels of tumor necrosis factor-alpha, interleukin-1beta and interleukin-6 were significantly increased after 24 hours of exposure in comparison to sham exposed cell cultures.
Germ cells: In the culture medium of germ cells which were co-incubated with exposed Sertoli cells, lipid peroxidation was significantly increased compared to germ cells co-incubated with sham exposed Sertoli cells. Additionally, co-incubation of germ cells with exposed Sertoli cells, led to a significantly increased apoptosis rate in germ cells in comparison to germ cells co-incubated with sham exposed Sertoli cells.
The authors suggest that exposure of rat Sertoli cells could have increased the synthesis of cytokines and that these cytokines could have an influence on the spermatogenesis in rats.