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桑色素对小鼠T淋巴细胞体外活化、 增殖和细胞周期的影响
http://www.100md.com 《细胞与分子免疫学杂志》 2007年第3期
桑色素;,T细胞活化;,增殖;,细胞周期,,]桑色素;,T细胞活化;,增殖;,细胞周期,桑色素对小鼠T淋巴细胞体外活化、增殖和细胞周期的影响,1材料和方法,2结果,3讨论,参考文献:
     The effect of morin on activation, proliferation and cellcycle of murine T lymphocytes in vitro

    ZANG Ning, ZENG Yaoying*, HUANG Xiuyan, WANG Tong, YE Xueyi, ZHOU Jianguo, WANG Huiying

    Institute of Tissue Transplantation and Immunology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China

    [Abstract] AIM: To discover the effects of morin on the activation, proliferation and cellcycle of murine T lymphocytes in vitro. METHODS: Murine lymph nodederived T lymphocytes were separated and stimulated with concanavalin A (ConA) and different experimental groups were set by cocultured with morin of different final concentration. Flow cytometry (FCM) was used to detect the activation, proliferation [carboxylfluorescein diacetate, succinimide ester (CFDASE) staining] and cellcycle [propidium iodide(PI) staining] of T cells. RESULTS: After 6 h time of culture in vitro, the rate of CD69+ T cells in control group was (2.97±0.12)%, while it was significant higher in ConA group[(72.52±0.66)% (P<0.01)]. Morin could downregulate this rate at final concentration being 25, 50 and 100 μmol/L, with a peak at 100 μmol/L morin[(48.95±0.81)% (P<0.01)]. CFDASE staining showed that at 48 h and 72 h, the proliferation indexes (PI) of T cells in ConA group were (1.58±0.04) and (1.95±0.02), respectively. Morin could significantly decrease the PI value at all experimental concentration, with the peak effect at 100 μmol/L morin, which the PI for 48 h was (1.02±0.02) and (1.03±0.01) for 72 h (P<0.01). FCM analysis of PI staining implied that the percentage of S phase cells in ConA group was (27.05±0.39)%, significantly higher than that in control group (5.10±0.07)%; and the 25 and 50 μmol/L morin groups showed higher S phase cell rates. CONCLUSION: Morin can significantly inhibit ConA stimulated activation and proliferation of murine T lymphocytes, in which the S phase lagging may serve as one of the major mechanisms. ......

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