Ma Sha, Xu Jie, Wang Xue, Wu Qing-Yun, Cao Jiang, Li Zheng-Yu, Zeng Ling-Yu, Chen Chong, Xu Kai-Lin
Institution of Hematology, Xuzhou Medical College, Xuzhou 221002, Jiangsu Province, China.
Department of Hematology, The Affiliated Hospital of Xuzhou Medical College, Xuzhou 221002, Jiangsu Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2015 Aug;23(4):950-5. doi: 10.7534/j.issn.1009-2137.2015.04.008.
To investigate the effect of ADAM10 inhibitor GI254023X on the proliferation and apoptosis of acute T-lymphoblastic leukemia Jurkat cells and its mechanisms.
Jurkat cells were treated with different concentrations of GI254023X, the proliferation-inhibition curve was assayed and plotted by CCK-8 method, the cell viability and apoptosis was detected by flow cytometry with Annexin V and 7-AAD staining, the cleavage of Notch1 protein was determined by Western blot, the transcripts of anti-apoptotic genes BCL-2, MCL-1, BCL-xl and Notch1 target gene Hes-1 were detected by real-time PCR.
The GI254023X obviously inhibited the proliferation of Jurkat cells in concentration-dependent manner. As compared with the control group, the apoptosis of cells increased along with increment of GI254023X concentration. Compared with control group, the expression of Cleaved Notch1 was down-regulated while the expression of Notch1 was up-regulated in a time-dependent manner after the treatment with GI254023X. The levels of MCL-1 and Hes-1 mRNA transcripts in Jurkat cells were reduced in GI254023X treated group, but did not show obvious effect on the level of BCL-2 and BCL-xl mRNA transcripts.
GI254023X can remarkably inhibit proliferation and induce apoptosis of Jurkat cells. The inhibition of Notch1 activation and the down-regulation of apoptosis-related gene MCL-1 may be involved in the process of apoptosis.
探讨ADAM10抑制剂GI254023X对急性T淋巴细胞白血病Jurkat细胞增殖和凋亡的影响及其机制。
用不同浓度的GI254023X处理Jurkat细胞,采用CCK-8法检测并绘制增殖抑制曲线,通过Annexin V和7-AAD染色利用流式细胞术检测细胞活力和凋亡情况,用蛋白质免疫印迹法检测Notch1蛋白的裂解情况,用实时定量PCR检测抗凋亡基因BCL-2、MCL-1、BCL-xl和Notch1靶基因Hes-1的转录本。
GI254023X明显以浓度依赖性方式抑制Jurkat细胞的增殖。与对照组相比,细胞凋亡率随GI254023X浓度的增加而升高。与对照组相比,GI254023X处理后,裂解的Notch1表达下调,而Notch1表达呈时间依赖性上调。GI254023X处理组Jurkat细胞中MCL-1和Hes-1 mRNA转录水平降低,但对BCL-2和BCL-xl mRNA转录水平无明显影响。
GI254023X可显著抑制Jurkat细胞的增殖并诱导其凋亡。Notch1激活的抑制和凋亡相关基因MCL-1的下调可能参与了凋亡过程。