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Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect 被引量:5
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作者 DONG Juan Cong CHENG Guang Hui +4 位作者 SHAN Yu Xing WU Ning SHAO Ming Long LI Peng Wu jin shun zi 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2014年第1期27-34,共8页
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 ... 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. 展开更多
关键词 Ionizing radiation Neuropilin-1 (Nrpl) Regulatory T cells Signal molecule
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