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重复进行0.5 Gy的γ射线照射可减轻MRL-lpr/lpr小鼠的自身免疫性疾病,其机制为抑制CD3+CD4-CD8-B220+ T细胞增殖并上调CD4+CD25+Foxp3+调节性T细胞。

Repeated 0.5-Gy gamma irradiation attenuates autoimmune disease in MRL-lpr/lpr mice with suppression of CD3+CD4-CD8-B220+ T-cell proliferation and with up-regulation of CD4+CD25+Foxp3+ regulatory T cells.

作者信息

Tago Fumitoshi, Tsukimoto Mitsutoshi, Nakatsukasa Hiroko, Kojima Shuji

机构信息

Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki Noda-shi Chiba, 278-8510, Japan.

出版信息

Radiat Res. 2008 Jan;169(1):59-66. doi: 10.1667/RR1013.1.

Abstract

Tago, F., Tsukimoto, M., Nakatsukasa, H. and Kojima. S. Repeated 0.5 Gy Gamma Irradiation Attenuates Autoimmune Disease in MRL-lpr/lpr Mice with Suppression of CD3(+)CD4(-)CD8(-)B220(+) T-Cell Proliferation and with Up-regulation of CD4(+)CD25(+)Foxp3(+) Regulatory T Cells. Radiat. Res. 169, 59-66 (2008). MRL-lpr/lpr mice are used as a model of systemic lupus erythematosus. We previously reported attenuation of autoimmune disease in MRL-lpr/lpr mice by repeated gamma irradiation (0.5 Gy each time). In this study, we investigated the mechanisms of this attenuation by measuring the weight of the spleen and the population of highly activated CD3(+)CD4(-)CD8(-)B220(+) T cells, which are characteristically involved in autoimmune pathology in these mice. Splenomegaly and an increase in the percentage of CD3(+)CD4(-)CD8(-)B220(+) T cells, which occur with aging in nonirradiated mice, were suppressed in irradiated mice. The high proliferation rate of CD3(+)CD4(-)CD8(-)B220(+) T cells was suppressed in the irradiated animals. The production of autoantibodies and the level of IL6, which activates B cells, were also lowered by radiation exposure. These results indicate that progression of pathology is suppressed by repeated 0.5-Gy gamma irradiation. To uncover the mechanism of the immune suppression, we measured the regulatory T cells, which suppress activated T cells and excessive autoimmune responses. We found that regulatory T cells were significantly increased in irradiated mice. We therefore conclude that repeated 0.5-Gy gamma irradiation suppresses the proliferation rate of CD3(+)CD4(-)CD8(-)B220(+) T cells and the production of IL6 and autoantibodies and up-regulates regulatory T cells.

摘要

田古,F.,筑本,M.,中塚,H. 及小岛,S. 重复0.5 Gyγ射线照射可减轻MRL-lpr/lpr小鼠的自身免疫性疾病,同时抑制CD3(+)CD4(-)CD8(-)B220(+) T细胞增殖并上调CD4(+)CD25(+)Foxp3(+)调节性T细胞。《辐射研究》169, 59 - 66 (2008年)。MRL-lpr/lpr小鼠被用作系统性红斑狼疮的模型。我们之前报道过重复γ射线照射(每次0.5 Gy)可减轻MRL-lpr/lpr小鼠的自身免疫性疾病。在本研究中,我们通过测量脾脏重量以及高度活化的CD3(+)CD4(-)CD8(-)B220(+) T细胞群体来探究这种减轻作用的机制,这些细胞在这些小鼠的自身免疫病理过程中具有特征性作用。在未照射的小鼠中,随着年龄增长会出现脾肿大以及CD3(+)CD4(-)CD8(-)B220(+) T细胞百分比增加,而在照射过的小鼠中这些现象受到了抑制。照射过的动物中CD3(+)CD4(-)CD8(-)B220(+) T细胞的高增殖率也受到了抑制。辐射暴露还降低了自身抗体的产生以及激活B细胞的IL6水平。这些结果表明,重复0.5 Gyγ射线照射可抑制病理进程。为了揭示免疫抑制的机制,我们测量了调节性T细胞,其可抑制活化的T细胞和过度的自身免疫反应。我们发现照射过的小鼠中调节性T细胞显著增加。因此我们得出结论,重复0.5 Gyγ射线照射可抑制CD3(+)CD4(-)CD8(-)B220(+) T细胞的增殖率、IL6和自身抗体的产生,并上调调节性T细胞。

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