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作 者:方敏[1] 毕可红[2] 姜国胜[3] 朱传升[2]
机构地区:[1]山东大学医学院,济南250012 [2]山东大学附属千佛山医院血液内科,济南250014 [3]山东省医学科学院基础医学研究所,济南250062
出 处:《山东大学学报(医学版)》2014年第2期1-5,共5页Journal of Shandong University:Health Sciences
基 金:国家自然科学基金(30771103);山东省自然科学基金(Y2008C165)
摘 要:目的研究急性髓系白血病细胞HL-60诱导分化后抗原处理相关转运体蛋白(TAP)及低分子量蛋白酶体(LMP)在该细胞模型中的表达变化及其意义。方法本实验分对照组、ATRA诱导组和PMA诱导组;Wright-Gimesa染色观察HL-60细胞形态,流式细胞术检测细胞表面标记CD11b、CD14的表达,RT-PCR检测LMP/TAP在mRNA水平的表达,Western blotting检测细胞TAP2基因的蛋白表达。结果 0.8μmol/L全反式维甲酸(ATRA)和50 nmol/L乙酸肉豆蔻佛波酯(PMA)分别作用HL-60细胞72 h后可显著抑制细胞增殖,并诱导细胞向成熟粒细胞及巨噬细胞方向分化;CD11b和CD14表达水平均明显升高(P均<0.05);TAP/LMP的mRNA表达水平及TAP2的蛋白表达水平均升高(P均<0.05)。结论白血病来源的单核样细胞具有一定的免疫功能表型,为进一步研究LMP/TAP在白血病免疫逃逸中的作用奠定基础。Objective To investigate the expression and significance of low molecular weight poly-peptide (LMP) and transporter associated with antigen processing (TAP) in leukemia cells HL-60 after induced differentiation. Methods The cells were divided into the control group, ATRA-induced goup and PMA-induced group. Cell morphology was observed by Wright-Giemsa staining. The expressions of cell surface markers CDllb and CD14 were measured by flow cytometry. TAP1, TAP2, LMP2 and LMP7 mRNA were measured by RT-PCR, and TAP2 proteins were determined by Western blotting. Results After treated for 72 hours, 0.8 μmol/L all-trans retinoic acid (ATRA) and 50 nmol/L phorbol myristate acetate (PMA) restrained the HL-60 cell proliferation and induced the cells to differentiate into the mature granulocyte and mononuclear macrophages; the expression levels of CDllb and CD14 significantly increased ( all P 〈 0.05 ) ; there were significant changes in the expressions of TAP1, TAP2, LMP2, and LMF7 mRNA ( all P 〈 0.05) ; the protein expression level of TAP2 was obviously decreased ( P 〈 0.05 ). Conclusion Leukemia-derived mononuclear cells have certain immune function phenotype, which lay the foundation for further study of LMP/TAP in leukemia immune escape.
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