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首页|期刊导航|山东医药|STAT1信号通路在全反式维甲酸诱导人白血病细胞向粒细胞分化过程中的作用与机制

STAT1信号通路在全反式维甲酸诱导人白血病细胞向粒细胞分化过程中的作用与机制

孙琳琳 姜国胜 李霞 郭强 朱肖肖 张振 赵霖 魏然 施引 尹训强 张云虹

山东医药2018,Vol.58Issue(6):24-27,4.
山东医药2018,Vol.58Issue(6):24-27,4.DOI:10.3969/j.issn.1002-266X.2018.06.006

STAT1信号通路在全反式维甲酸诱导人白血病细胞向粒细胞分化过程中的作用与机制

Role and molecular mechanism of STAT1 signaling pathway in the differentiation of leukemia cells into granulocytes induced by all-trans retinoic acid

孙琳琳 1姜国胜 2李霞 2郭强 2朱肖肖 2张振 2赵霖 2魏然 2施引 2尹训强 1张云虹2

作者信息

  • 1. 济南大学山东省医学科学院医学与生命科学学院,济南250200
  • 2. 山东省医学科学院基础医学研究所
  • 折叠

摘要

Abstract

Objective To detect the role and regulatory mechanism of signal transducer and activator of transcription 1 (STAT1) in promoting the differentiation of human leukemia cells into granulocytes induced by all-trans retinoic acid (ATRA),and to provide a novel target for clinical treatment.Methods Human acute myeloid leukemia cells HL-60 were randomly divided into the control group and observation group.In the observation group,HL-60 cells were induced to differentiate into granulocytics with ATRA (2 μmol/L),while cells in the control group were given the same concentration of DMSO.Morphologic changes of cells were observed by Wright-Giemsa staining.Cell surface marker CD11b was detected by flow cytometry.The mRNA expression levels of STAT1 and CCAAT/enhancer binding proteinsε (C/EBPε) were detected by q-PCR,the protein and phosphorylation levels of STAT1 (p-STAT1) were detected by Western blotting,and the transcriptional level of miR-155-5p was detected by q-PCR.Pearson correlation analysis was used to detect the correlation of STAT1 with C/EBPε and miR-155-5p.Results Compared with the control group,the HL-60 cells in the observation group became smaller and irregular,cytoplasm increased,nuclear concentrated,nucleolus became smaller or disappeared,and the number of leaf nuclei increased significantly.The rate of CD1 1b positive HL-60.cells in the observation group at 96 h after ATRA induction was 62.97% ± 1.90%,which was higher than that in the control group (1.87% ±0.08%) (P < 0.05).Compared with the control group,the mRNA expression levels of STAT1 and C/EBPε,and the protein expression levels of STAT1 and p-STAT1 in the observation group at 48,72,and96 h after ATRA induction increased (all P < 0.05),while the expression of miR-155-5p decreased (P < 0.05).Pearson correlation analysis showed that STAT1 mRNA was negatively correlated with miR-155-5p (r =-0.90,P <0.05),while was positively correlated with C/EBPε mRNA (r =0.96,P < 0.05).Conclusions The miR-155-5p reversely regulates STAT1 signaling pathway,thus activates the transcription of C/EBPε,which leads to the differentiation of HL-60 cells into granulocytes.Activation of STAT1 signaling pathway may be one of the key mechanisms in the differentiation of HL-60 cells into granulocytes,and STAT1 may be taken as a novel target for clinical treatment.

关键词

人急性髓系白血病细胞/HL-60细胞/粒细胞/全反式维甲酸/信号转导与转录激活因子1/微小RNA-155-5p/亮氨酸结构拉链转录因子ε

Key words

human acute myeloid leukemia cells/HL-60 cells/granulocytes/all-trans retinoic acid/signal transducer and activator of transcription 1/microRNA-155-5p/CCAAT/enhancer binding proteins ε

分类

医药卫生

引用本文复制引用

孙琳琳,姜国胜,李霞,郭强,朱肖肖,张振,赵霖,魏然,施引,尹训强,张云虹..STAT1信号通路在全反式维甲酸诱导人白血病细胞向粒细胞分化过程中的作用与机制[J].山东医药,2018,58(6):24-27,4.

基金项目

国家自然科学基金资助项目(81373670,81573467) (81373670,81573467)

山东省重点研发项目(2016GSF202016) (2016GSF202016)

山东省自然科学基金资助项目(ZR2015HM014,ZR2017PH008). (ZR2015HM014,ZR2017PH008)

山东医药

OACSTPCD

1002-266X

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