Volume 27 Issue 1
Jan.  2014
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DONG Juan Cong, CHENG Guang Hui, SHAN Yu Xing, WU Ning, SHAO Ming Long, LI Peng Wu, JIN Shun Zi. Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect[J]. Biomedical and Environmental Sciences, 2014, 27(1): 27-34. doi: 10.3967/bes2014.005
Citation: DONG Juan Cong, CHENG Guang Hui, SHAN Yu Xing, WU Ning, SHAO Ming Long, LI Peng Wu, JIN Shun Zi. Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect[J]. Biomedical and Environmental Sciences, 2014, 27(1): 27-34. doi: 10.3967/bes2014.005

Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect

doi: 10.3967/bes2014.005
Funds:  grants from the National Natural Science Foundation of China(30870584, 81201737)%the Doctoral Program Foundation of Institutions of Higher Education of China(20120061110063)
  • Objective The purpose of the present study was to observe the changes in CD4+CD25+Nrp1+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, Nrp1, calcineurin and PKC-α were detected by flow cytometry. The expressions of TGF-β1, IL-10, PKA and cAMP were estimated with ELISA.
    Results At 12 h after irradiation, the expression of Nrp1 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-10) 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+Nrp1+Treg cells after ionizing radiation.
    Conclusion These results indicated that HDR might induce CD4+CD25+Nrp1+Treg cells production and stimulate TGF-β1 secretion by regulating signal molecules in mice.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect

doi: 10.3967/bes2014.005
Funds:  grants from the National Natural Science Foundation of China(30870584, 81201737)%the Doctoral Program Foundation of Institutions of Higher Education of China(20120061110063)

Abstract: Objective The purpose of the present study was to observe the changes in CD4+CD25+Nrp1+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, Nrp1, calcineurin and PKC-α were detected by flow cytometry. The expressions of TGF-β1, IL-10, PKA and cAMP were estimated with ELISA.
Results At 12 h after irradiation, the expression of Nrp1 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-10) 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+Nrp1+Treg cells after ionizing radiation.
Conclusion These results indicated that HDR might induce CD4+CD25+Nrp1+Treg cells production and stimulate TGF-β1 secretion by regulating signal molecules in mice.

DONG Juan Cong, CHENG Guang Hui, SHAN Yu Xing, WU Ning, SHAO Ming Long, LI Peng Wu, JIN Shun Zi. Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect[J]. Biomedical and Environmental Sciences, 2014, 27(1): 27-34. doi: 10.3967/bes2014.005
Citation: DONG Juan Cong, CHENG Guang Hui, SHAN Yu Xing, WU Ning, SHAO Ming Long, LI Peng Wu, JIN Shun Zi. Role of PLC-PIP2 and cAMP-PKA Signal Pathways in Radiation-induced Immune-suppressing Effect[J]. Biomedical and Environmental Sciences, 2014, 27(1): 27-34. doi: 10.3967/bes2014.005

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