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作 者:危敏[1] 石嵘[1] 姜立[2] 王妮莎[1] 马文丽[1]
机构地区:[1]南方医科大学基因工程研究所,广东广州510515 [2]广东省人民医院科教处,广东广州510080
出 处:《南方医科大学学报》2012年第12期1689-1694,共6页Journal of Southern Medical University
基 金:国家自然科学基金(30901721)~~
摘 要:目的建立稳定抑制水通道蛋白1(AQP1)表达的K562细胞株,探讨AQP1在维甲酸(RA)诱导红白血病细胞红系分化中的作用。方法 RA处理K562细胞,通过real-time PCR法检测γ-珠蛋白表达和分光光度法检测血红蛋白的含量研究RA对K562细胞红系分化的影响。Real-time PCR法、蛋白质印迹法检测RA诱导后K562细胞AQP1转录和蛋白表达水平的变化。设计特异AQP1 shRNA序列,构建pSUPER-retro-puro重组质粒转染K562细胞,筛选建立稳定抑制AQP1基因表达的K562细胞株(K562-shAQP1);通过比较K562-shAQP1细胞株与对照组细胞在维甲酸诱导后γ-珠蛋白和血红蛋白的表达,研究AQP1在维甲酸诱导K562细胞红系分化中的作用。结果 RA处理K562细胞后红系分化指标γ-珠蛋白和血红蛋白的表达均明显增加,同时AQP1 mRNA及蛋白表达随RA作用时间显著增加(P<0.01)。pSUPER-retro-puro-shAQP1干扰载体转染K562细胞后AQP1基因在转录和蛋白水平上的表达均被抑制,差异有统计学意义(P<0.01);K562-shAQP1细胞与对照K562细胞相比,在RA诱导后γ-珠蛋白和血红蛋白表达受到不同程度的抑制,差异有统计学意义(P<0.01)。结论 RA诱导K562细胞红系分化后AQP1表达显著增加,而抑制AQP1基因的表达可部分阻断RA诱导红系分化的作用,说明AQP1在RA诱导K562细胞红系分化过程中发挥重要作用。Objective To explore the role of aquaporin-1 (AQP1) gene in erythroid differentiation of erythroleukemia K562 cells induced by retinoic acid (RA). Methods K562 cells were cultured in the presence of 1μmol/L RA for varying lengths of time, and y-globin mRNA expression and hemoglobin content in the ceils were detected by real-time PCR (RT-PCR) and ultraviolet spectrophotometry, respectively, to evaluate the erythroid differentiation of K562 cells. RT-PCR and Western blotting were used to examine AQP1 expression in the cells following RA treatment. A retroviral expression vector of AQP1 small interfering RNA (pSUPER-retro-puro-shAQP1) was constructed and transfected into K562 cells to establish a K562 cell line with stable AQP1 down-regulation (K562-shAQP1), in which the changes in y-globin and hemoglobin expressions after RA treatment were detected. Results RA treatment significantly increased y-globin and hemoglobin expressions in K562 cells (P〈0.01), causing also significantly enhanced AQP1 mRNA and protein expressions over time (P〈0.01). Transfection with the recombinant plasmids pSuper-retro-puro-shAQP1 resulted in stable AQP1 suppression in K562 cells (P〈0.01), which showed markedly reduced γ-globin and hemoglobin expressions after RA induction as compared to the control K562 cells (P〈0.01). Conclusions K562 cells show a significant increase of AQP1 expression after RA-induced erythroid differentiation, and suppression of AQP1 expression can partially block the effect of RA, suggesting the important role of AQP1 in RA-induced erythroid differentiation of K562 ceils.
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