Wei Min, Shi Rong, Jiang Li, Wang Nisha, Ma Wenli
Institute of Genetic Engineering, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2012 Dec;32(12):1689-94.
To explore the role of aquaporin-1 (AQP1) gene in erythroid differentiation of erythroleukemia K562 cells induced by retinoic acid (RA).
K562 cells were cultured in the presence of 1 µmol/L RA for varying lengths of time, and γ-globin mRNA expression and hemoglobin content in the cells 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 γ-globin and hemoglobin expressions after RA treatment were detected.
RA treatment significantly increased γ-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).
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 cells.
探讨水通道蛋白-1(AQP1)基因在维甲酸(RA)诱导红白血病K562细胞红系分化中的作用。
将K562细胞在1 μmol/L RA存在的条件下培养不同时间,分别采用实时荧光定量PCR(RT-PCR)和紫外分光光度法检测细胞中γ-珠蛋白mRNA表达及血红蛋白含量,以评估K562细胞的红系分化情况。采用RT-PCR和蛋白质免疫印迹法检测RA处理后细胞中AQP1的表达。构建AQP1小干扰RNA逆转录病毒表达载体(pSUPER-retro-puro-shAQP1)并转染至K562细胞,建立稳定下调AQP1的K562细胞系(K562-shAQP1),检测RA处理后该细胞系中γ-珠蛋白和血红蛋白表达的变化。
RA处理显著增加了K562细胞中γ-珠蛋白和血红蛋白的表达(P<0.01),且随着时间的推移,AQP1 mRNA和蛋白表达也显著增强(P<0.01)。转染重组质粒pSuper-retro-puro-shAQP1可使K562细胞中AQP1稳定下调(P<0.01),与对照K562细胞相比,RA诱导后该细胞系中γ-珠蛋白和血红蛋白表达明显降低(P<0.01)。
RA诱导K562细胞红系分化后AQP1表达显著增加,抑制AQP1表达可部分阻断RA的作用,提示AQP1在RA诱导K562细胞红系分化中起重要作用。