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丹参酮IIA与全反式维甲酸协同诱导NB4细胞分化及凋亡

[Differentiation and apoptosis of NB4 cells synergistically induced by Tanshinone II A and all-trans retinoic acid].

作者信息

Liu Zhi-gang, Yang Yi-ming, Meng Wen-tong, Huang Chun-lan

机构信息

Department of Hematology, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2004 Nov;35(6):788-91.

Abstract

OBJECTIVE

To evalutate the synergistic effects of Tanshinone II A combined with all-trans retinoic acid (ATRA) on the differentiation and apoptosis of human acute promyelocytic leukemia (APL) cell line (NB4).

METHODS

The NB4 cells were treated with 0.5 microg/ml Tanshinone II A combined with 0.5 microg/ml, 0.25 microg/ml and 0.125 microg/ml ATRA respectively in culture. Cells differentiation was demonstrated by morphology and NBT reduction assay. The expression of CD11b and CD33, cell cycle and apoptosis induced by these drugs were measured by flow cytometry (FCM).

RESULTS

The proliferative inhibition rate of the combination of Tan II A with ATRA was much higher. The differentiated cells accounted for over 90 percent, among them the band forms and neutrophils constituted more than 65 percent. NBT reduction and CD11b expression were much higher, and expression of CD33 was lower than that of Tan II A or ATRA alone (P<0.01). FCM analysis also showed that combination of Tan II A with ATRA arrested NB4 cells in G0/G1 phase and induced significantly apoptosis of NB4 cells (P<0.01). There were no significant dose dependent effects induced by ATRA in combination with Tan II A at 0.125 microg/ml to 0.5 microg/ml on differentiation and apoptosis of NB4 cells.

CONCLUSION

The combination of Tan II A with ATRA has synergistic effects on differentiation and apoptosis of NB4 cells. The effects do not increase with the dosage escalation of ATRA.

摘要

目的

评估丹参酮ⅡA联合全反式维甲酸(ATRA)对人急性早幼粒细胞白血病(APL)细胞系(NB4)分化及凋亡的协同作用。

方法

将NB4细胞在培养中分别用0.5μg/ml丹参酮ⅡA与0.5μg/ml、0.25μg/ml和0.125μg/ml ATRA处理。通过形态学及NBT还原试验证明细胞分化情况。采用流式细胞术(FCM)检测这些药物诱导的CD11b和CD33表达、细胞周期及凋亡情况。

结果

丹参酮ⅡA与ATRA联合应用的增殖抑制率更高。分化细胞占90%以上,其中杆状核及中性粒细胞占65%以上。NBT还原及CD11b表达更高,而CD33表达低于单独使用丹参酮ⅡA或ATRA(P<0.01)。FCM分析还显示,丹参酮ⅡA与ATRA联合使NB4细胞停滞于G0/G1期并显著诱导NB4细胞凋亡(P<0.01)。0.125μg/ml至0.5μg/ml的ATRA与丹参酮ⅡA联合应用对NB4细胞的分化及凋亡无明显剂量依赖性效应。

结论

丹参酮ⅡA与ATRA联合对NB4细胞的分化及凋亡具有协同作用。该作用并不随ATRA剂量增加而增强。

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