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作 者:周磊[1] 何奔[1] 沈玲红[1] 曾锦章[2] 胡刘华[1] 卜军[1] 王力[2]
机构地区:[1]上海交通大学医学院附属仁济医院心内科,上海市200127 [2]中国科学院上海生命科学研究所,上海市200233
出 处:《中国动脉硬化杂志》2008年第9期673-676,共4页Chinese Journal of Arteriosclerosis
基 金:国家自然科学基金(30670880和30600242);上海市科委基础研究重点项目(05JC14037和08XD1402600)
摘 要:目的探讨视黄醇类X受体特异性激动剂9-顺式维甲酸对佛波酯诱导人单核细胞系THP-1向巨噬细胞分化的影响。方法体外培养人单核细胞系THP-1,经佛波酯诱导分化为巨噬细胞,同时给予9-顺式维甲酸对佛波酯诱导分化进行干预,通过相差显微镜观察细胞形态,MTT比色法检测细胞贴壁率,流式细胞仪检测与单核/巨噬细胞分化有关的细胞表面标志物CD11b和CD36的表达。结果9-顺式维甲酸干预后梭形、分支状细胞明显减少,与佛波酯单独作用组相比细胞贴壁率减少50%(P<0.01),细胞表面标志物CD11b和CD36分别减少50%和28%(P<0.01)。结论视黄醇类X受体特异性激动剂9-顺式维甲酸可明显抑制佛波酯诱导人单核细胞系THP-1向巨噬细胞分化。Aim To investigate the effect of 9-cis-retinoid acid (9-cisRA), a specific agonist of retinoid X receptors (RXR) on the differentiation of THP-1 human monocyte cell induced by phorbol-12-myristate-13-acetate (PMA). Methods Human monocyte cell line THP-1 was cultured and induced to macrophage by PMA treatment. The effect of 9-cisRA on the differentiation induced by PMA was studied. Cell morphology was observed by phase contrast microscope and the adhesion rate of THP-1 was detected by methyl thiazolyltetrazolium (MTT) assay. The cell surface markers involved in differentiation of monocyte/macrophage (CD11b, CD36) were analyzed by flow cytometry (FACS). Results The metamorphotic cells were decreased in 9-cisRA group. THP-1 cell adhesion rate was inhibited by 50% (P〈0.01), and the cell surface markers (CD11b, CD36) were decreased by 50% and 28% (P〈0.01) in 9-cisRA treated group. Conclusion The specific agonist of RXR, 9-cisRA could effectively inhibit the differentiation of THP-1 human monocyte induced by PMA.
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