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人脐带间充质干细胞增强全反式维甲酸对HL-60细胞的诱导分化作用
引用本文:吴昊,马凤霞,李建平,杨少光,贾海蓉,卢世红,任倩,赵钦军,刑文,张磊,韩忠朝.人脐带间充质干细胞增强全反式维甲酸对HL-60细胞的诱导分化作用[J].中国实验血液学杂志,2010,18(4):877-881.
作者姓名:吴昊  马凤霞  李建平  杨少光  贾海蓉  卢世红  任倩  赵钦军  刑文  张磊  韩忠朝
作者单位:中国医学科学院、北京协和医学院血液学研究所、血液病医院实验血液学国家重点实验室,天津,300020
基金项目:国家自然科学基金项目,国家自然科学基金项目 
摘    要:本研究探讨人脐带间充质干细胞(hucMSC)对全反式维甲酸(ATRA)诱导HL-60细胞分化以及对HL-60增殖的影响。HL-60细胞分为4组:未经ATRA处理的对照组、与hucMSC细胞共培养的hucMSC组,经ATRA处理的ATRA组以及经ATRA处理并与hucMSC细胞共培养的ATRA+hucMSC组。在规定时间采用Cell Counting Kit-8(CCK8)检测对照组和hucMSC组HL-60细胞增殖情况;在光学显微镜下观察各组细胞形态、NBT阳性细胞;应用real-timePCR方法检测c-myc基因表达水平以及流式细胞术检测CD11b表面标志以比较各组中HL-60细胞的分化情况。结果表明:共培养体系中hucMSC细胞能抑制HL-60的增殖,hucMSC∶HL-60为1∶1时,48小时时p0.05,72小时时p0.01;hucMSC∶HL-60为1∶5时,72小时时p0.05。在2μmol/LATRA的刺激下,ATRA+huc-MSC组与ATRA组相比,出现更多具有中性粒细胞形态的HL-60细胞和更高的NBT阳性率(p0.05);ATRA+hucMSC组中HL-60细胞c-myc基因表达更低(p0.05);ATRA+hucMSC组中HL-60细胞CD11b的表达更高(48小时p0.05,72小时p0.01)。结论:脐带间充质干细胞能抑制HL-60增殖并且增强ATRA对HL-60细胞的诱导分化作用。

关 键 词:脐带间充质干细胞  HL-60  全反式维甲酸  诱导分化  中性粒细胞

Enhancement of All-trans Retinoic Acid Induced HL-60 Leukemia Cell Differentiation by Human Umbilical Cord Mesenchymal Stem Cells
WU Hao,MA Feng-Xia,LI Jian-Ping,YANG Shao-Guang,JIA Hai-Rong,LU Shi-Hong,REN Qian,ZHAO Qin-Jun,XING Wen,ZHANG Lei,HAN Zhong-Chao.Enhancement of All-trans Retinoic Acid Induced HL-60 Leukemia Cell Differentiation by Human Umbilical Cord Mesenchymal Stem Cells[J].Journal of Experimental Hematology,2010,18(4):877-881.
Authors:WU Hao  MA Feng-Xia  LI Jian-Ping  YANG Shao-Guang  JIA Hai-Rong  LU Shi-Hong  REN Qian  ZHAO Qin-Jun  XING Wen  ZHANG Lei  HAN Zhong-Chao
Institution:( State Key Laboratory of Experimental Hematology, Institute of Hematology &Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China)
Abstract:This study was aimed to investigate the enhancement of all-trans retinoic acid-induced HL-60 leukemia cell differentiation by human umbilical cord mesenchymal stem cells (hucMSC). The HL-60 cells were divided into 4 groups: control group (HL-60 cells treated without ATRA), hucMSC group (HL-60 cells co-cultured with hucMSCs), ATRA group (HL-60 cells treated with ATRA) and ATRA + hucMSC group (HL-60 cells treated with ATRA and co- cultcured with hucMSCs). The proliferations of control group and hucMSC group were compared by Cell Counting Kit- 8 ( CCK8 ). The morphology of HL-60 cells and NBT positive rate in 4 groups were observed and compared by means of microscopy, the c-myc expression of HL-60 cells in different groups was evaluated by real-time PCR, and the CDllb expression on HL-60 cells in different groups were detected by flow cytometry. The results showed that in the co-culturing system, hucMSCs could inhibit the proliferation of HL-60 ( hucMSC: HL-60 is 1 : 1, 48 hours p 〈 0.05, 72 hours p 〈 0.01 ; hucMSC: HL-60 is 1 : 5, 72 hours p 〈 0.05 ). In condition of stimulation with 2 μmol/L ATRA, the neutrophil like HL-60 cells and NBT positive rate in ATRA + hucMSC group were higher than those in ATRA group (p 〈 0.05 ). The c-myc expression of HL-60 cells in ATRA + hucMSC group was lower than that in ATRA group (p 〈0.05 ). Furthermore, HL-60 cells in ATRA + hucMSC group had stronger CD1 lb expression than ATRA group (48 hours p 〈 0.05, 72 hours p 〈0.01 ). It is concluded that hucMSC not only can inhibit the proliferation of HL-60 cells, but also can enhance the differentiation effect of HL-60 cells induced by ATRA.
Keywords:HL-60
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