现在的学习的目的是与不同剂量在照耀以后在 CD4+CD25+Nrp1+Treg 房间观察变化并且探索包含的可能的分子的机制的目的。方法 ICR 老鼠和老鼠淋巴瘤房间线(EL-4 房间) 被使用。CD4, CD25, Nrp1, calcineurin 和 PKC- 的表情被流动 cytometry 检测。TGF-1, IL-10, PKA 和营地的表情与 ELISA 被估计。在在照耀以后的 12 h 的结果, Nrp1 的表达式在 4.0 Gy 组显著地增加了,与假冒照耀的组相比(P < 0.05 ) 在怒气和胸腺,分别地当 ICR 鼠标收到了整个身体的照耀(WBI ) 时。同时, Interleukin 10 (IL-10 ) 和转变生长 factor-1 (TGF-1 ) 的合成在高剂量照耀(HDR ) 以后显著地增加了(> 或 = 1.0 Gy ) 。另外,,营地的表示和 PKA 蛋白质增加了 PKC- , calcineurin 在 4.0 Gy X 照耀以后在胸腺房间在 12h 减少了。当当 PLC-PIP2 信号小径被刺激或 cAMP-PKA 信号小径在 4.0 Gy X 照耀以后被堵住时, TGF-1 清楚地被禁止时,这没在电离以后限制 CD4+CD25+Nrp1+Treg 房间的起来规定放射。这些结果显示了那 HDR 的结论可能导致 CD4+CD25+Nrp1+Treg 房间生产并且由在老鼠调整信号分子刺激 TGF-1 分泌物。
Objective The purpose of the present study was to observe the changes in CD4+CD25+Nrpl+Treg cells after irradiation with different doses and explore the possible molecular mechanisms involved. Methods ICR mice and mouse lymphoma cell line (EL-4 cells) was used. The expressions of CD4, CD25, Nrpl, calcineurin and PKC-α were detected by flow cytometry. The expressions of TGF-131, IL-10, PKA and cAMP were estimated with ELISA. Results At 12 h after irradiation, the expression of Nrpl increased significantly in 4.0 Gy group, compared with sham-irradiation group (P〈0.05) in the spleen and thymus, respectively, when ICR mice received whole-body irradiation (WBI). Meanwhile the synthesis of Interleukin 10 (IL-20) and transforming growth factor-β1 (TGF-β1) increased significantly after high dose irradiation (HDR) (〉 or = 1.0 Gy). In addition, the expression of cAMP and PKA protein increased, while PKC-α, calcineurin decreased at 12h in thymus cells after 4.0 Gy X-irradiation. While TGF-β1 was clearly inhibited when the PLC-PIP2 signal pathway was stimulated or the cAMP-PKA signal pathway was blocked after 4.0 Gy X-irradiation, this did not limit the up-regulation of CD4+CD25+Nrpl+Treg cells after ionizing radiation. Conclusion These results indicated that HDR might induce CD4+CD25+Nrpl+Treg cells production and stimulate TGF-β1 secretion by regulating signal molecules in mice.