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脂多糖体外刺激对小鼠B10细胞的影响
引用本文:穆大为,张继刚,王玉真.脂多糖体外刺激对小鼠B10细胞的影响[J].中国医学装备,2013(4):25-27.
作者姓名:穆大为  张继刚  王玉真
作者单位:[1]空军总医院泌尿外科,北京100142 [2]第二炮兵总医院皮肤科,北京100088 [3]空军装备研究院门诊部,北京100085
摘    要:目的:探索脂多糖(LPS)体外刺激对小鼠B10细胞的影响。方法:在LPS刺激下,体外培养小鼠脾脏和腹腔细胞5h或48h,流式细胞仪分析CD19+IL-10+B细胞比例。结果:PIM刺激5h,小鼠脾脏和腹腔CD19+IL-10+B细胞比例分别升高至1.22%和14.82%(P<0.01),在PIM刺激的基础上加入LPS,小鼠脾脏和腹腔中CD19+IL-10+B细胞比例分别升高至平均2.35%和26.58%(P<0.01)。LPS刺激48h可进一步升高CD19+IL-10+B细胞比例,脾脏和腹腔分别为6.42%和38.38%,明显高于PIM48h刺激组(P<0.01)和L+PIM5h刺激组(P<0.05),但LPS刺激48h不改变CD5、CD1d的表达水平。结论:体外刺激5h时,L+PIM刺激可促进小鼠B10细胞活化;刺激48h时,LPS可进一步促进B10细胞IL-10的表达,这一作用可能是通过诱导B10前体细胞成熟实现的。

关 键 词:B10细胞  白介素-10  脂多糖  体外培养  流式细胞仪

The effect of LPS stimulation in vitro on B10 cells of mice
MU Da-wei,ZHANG Ji-gang,WANG Yu-zhen.The effect of LPS stimulation in vitro on B10 cells of mice[J].China Medical Equipment,2013(4):25-27.
Authors:MU Da-wei  ZHANG Ji-gang  WANG Yu-zhen
Institution:MU Da-wei, ZHANG Ji-gang, WANG Yu-zhen
Abstract:Abstract] Objective: To explore the influence of LPS stimulation in vitro on the B10 cells of mice. Methods: Spleen and Peritoneal cavity cells of mice were cultured in vitro with LPS stimulator for 5h or 48h, then analyzed the percentage of the CD19+IL-10+B cells with flow cytometry. Results: The percentages of CD19+IL-10+B cells in spleen and peritoneal cavity of mice were raised to 1.22% and 14.82% with PIM stimulation for 5h(P〈0.01). The mean percentages of CD19~IL-10+B cells in spleen and peritoneal cavity of mice after L+PIM stimulation for 5h were respectively 2.35% and 26.58%(P〈0.01). And the frequencies of CD19+IL-10+B cells after L+PIM stimulation for 48 h were respectively 6.42% and 38.38% and higher significantly than stimulation with PIM for 48 h(P〈0.01) and L+PIM stimulation for 5h(P〈0.05). However, L+PIM stimulation for 48h don't change the expression of CD5 and CDld of spleen B cells. Conclusion: L+PIM stimulation for 5h can pormote the activation of 10 cells of mice. LPS stimulation for 48h can further raise the expression of IL-10 in B10 cells of mice and this effect may be caused by inducing the maturation of B10pro in CD5+CD1dhhi B cell subset. Key words] B10 cells; Interleukino-10; LPS; Culture in vitro; Flow cytometry
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