Hu Yan, Li Jing, Wang Li-Hong, Xu Qian-Fei, Xia Rui-Xiang, Zeng Qing-Shu, Liu Xiao-Ying, Ge Jian
Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui Province, China.
Department of Biology, Life Science college of Anhui Medical University, Hefei 230032, Anhui Province, China.E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Oct;25(5):1300-1306. doi: 10.7534/j.issn.1009-2137.2017.05.005.
To study the expression of stromal cell derived factor-1α (SDF-1α) receptor CXCR7 in acute monocytic leukemia (AML-M5), and its effects on proliferation, apoptosis, invasion of acute monocytic leukemia cell line THP-1.
CXCR7 protein and mRNA expression levels in THP-1 cells and peripheral blood mononuclear cells (PBMNC) from the newly diagnosed AML-M5 patients and normal individuals were detected by flow cytometry, Western blot and RT-PCR respectively. CCK8, Annexin V/PI double staining and Transwell assay were used to observe the effects of CXCR7 on the proliferation, apoptosis, and invasion of THP-1 cells in vitro.
The expression of CXCR7 on immature cell surface of the newly diagnosed AML-M5 patients was significantly higher than that in the control group (P<0.05). CXCR7 was also highly expressed on THP-1 cells surface. The CXCR7 protein and mRNA levels in THP-1 cells and PBMNC of AML-M5 patients were significantly higher than those in the control group (P<0.05). The THP-1 cell proliferation activity was higher in SDF-1α-treated group, but this activity could be inhibited by CXCR7 antibody (P<0.01). CXCR7 antibody did not affect THP-1 cell apoptosis (P>0.05). CXCR7 antibody could inhibit SDF-1α -induced THP-1 cell invasiveness (P<0.01).
CXCR7 highly expresses in AML-M5 patients and THP-1 cells, and involves in cell proliferation and invasion. The blocking CXCR7 expression can reduce the risk of AML-M5 cell infiltration.
研究基质细胞衍生因子-1α(SDF-1α)受体CXCR7在急性单核细胞白血病(AML-M5)中的表达情况,及其对急性单核细胞白血病细胞系THP-1增殖、凋亡、侵袭的影响。
分别采用流式细胞术、蛋白质免疫印迹法及逆转录-聚合酶链反应(RT-PCR)检测新诊断AML-M5患者及正常个体外周血单个核细胞(PBMNC)和THP-1细胞中CXCR7蛋白及mRNA表达水平。采用细胞计数试剂盒-8(CCK8)法、膜联蛋白V/碘化丙啶(Annexin V/PI)双染法及Transwell小室实验观察CXCR7对THP-1细胞体外增殖、凋亡及侵袭的影响。
新诊断AML-M5患者未成熟细胞表面CXCR7表达明显高于对照组(P<0.05)。THP-1细胞表面CXCR7也呈高表达。AML-M5患者THP-1细胞及PBMNC中CXCR7蛋白及mRNA水平明显高于对照组(P<0.05)。SDF-1α处理组THP-1细胞增殖活性较高,但该活性可被CXCR7抗体抑制(P<0.01)。CXCR7抗体不影响THP-1细胞凋亡(P>0.05)。CXCR7抗体可抑制SDF-1α诱导的THP-1细胞侵袭能力(P<0.01)。
CXCR7在AML-M5患者及THP-1细胞中高表达,参与细胞增殖和侵袭过程。阻断CXCR7表达可降低AML-M5细胞浸润风险。