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大鼠慢性非细菌性前列腺炎模型中调节性T淋巴细胞表达的变化及意义 被引量:4

Change and significance of the regulatory T lymphocytes expression in rats model of chronic abacterial prostatitis
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摘要 目的探讨调节性T淋巴细胞在大鼠慢性非细菌性前列腺炎模型外周血中的变化及意义。方法2011年12月至2012年7月,390g左右的Wistar雄性大鼠12只采用简单随机抽样法平均分为实验组和对照组。实验组大鼠行去势术,术后皮下注射17-β雌二醇(0.25mg/d,连续30d)建立慢性非细菌性前列腺炎模型,对照组大鼠饲养30d后同实验组一起处理。建模成功后,用流式细胞仪检测大鼠外周血中CD4+CD25+T淋巴细胞群比例和CD8+CD28-T淋巴细胞群比例的变化。结果实验组CD4+CD25+T淋巴细胞群比例(7.90±1.74)%与对照组(11.63±1.36)%相比明显下降(P〈0.01)。实验组CD8+CD28-T淋巴细胞群比例(17.18±2.83)%与对照组(24.64±4.76)%相比也有所下降,差异有统计学意义(P〈0.01)。结论大鼠慢性非细菌性前列腺炎模型外周血中cD:cD+5T淋巴细胞群比例和CD8+CD28-T淋巴细胞群比例的变化可能为调节性T淋巴细胞参与大鼠慢性非细菌性前列腺炎的致病机制提供证据。、 Objective To investigate the change and significance of regulatory T lymphocytes in pe- ripheral blood of rats model of chronic abacterial prostatitis. Methods Twelve Wistar rats with weight of approximate 390 g were randomly divided into two groups, model group and control group. Rats in the model group was injected subcutaneously 17β-estradiol(0.25 rag/day, for 30 days) after castration to establish rat model of chronic abacterial prostatitis. Flow cytometry was applied to detect the frequency of CD4+ CD25+T cells and CD8+CD28-T cells in peripheral blood of rats after model establishment. Results Compared with control group ( 11.63± 1.36) %, the proportion of CD4+ CD25+T T lymphocytes in model group ( 7.90± 1.74) % significanhy decreased (P〈0.01). Compared with control group (24.64±4.76)%, the proportion of CD8+CD28-T lymphocytes in model group (17.18±2.83)% also significantly decreased (P〈0.01). Conclusions The changes of the ratio of CD4+ CD25+T lymphocytes and CD8+CD28-T lymphocytes in peripheral blood of rats model of chronic abacterial prostatitis provided evidences for pathogenic mechanism of regulatory T lymphocytes participating in the development of chronic abaeterial prostatitis.
出处 《中华泌尿外科杂志》 CAS CSCD 北大核心 2013年第8期622-626,共5页 Chinese Journal of Urology
关键词 慢性非细菌性前列腺炎 疾病模型 动物 T细胞 调节性 CD4+CD25+T细胞 CD8+CD28-T细胞 Chronic abacterial prostatitis Disease models, animal Regulatory T lymphocytes CD4+ CD25+T tymphocytes CD8+CD28-T lymphocytes
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