Tang Hui-Min, Ding Wei, Ding Yi-Han, Wu Jing-Jing, Li Yu-Feng
Department of Hematology, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian 223300, Jiangsu Province, China.
Department of Respiratory diseases, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian 223300, Jiangsu Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Apr;27(2):379-384. doi: 10.19746/j.cnki.issn.1009-2137.2019.02.011.
To explore the the effects of ubiquitin-proteasome system (UPS) on BCL6 protein level,proliferation and apoptosis of cell imatinib(IM)-resistant K562/G01 cells.
Western blot was used to detect the expression of BCL6 in K562/G01 cells before and after treatment with protease inhibitor MG-132.The RT-PCR and Western blot respectively were used to detect the mRNA and protein expression levels of BCL6 and USP2 in K562/G01 cells treated with or without ML364 (a ubiquitin-specific protease USP2 inhibitor). The effects of IM alone or in combination with ML364 on proliferation and apoptosis of K562/G01 were analysed by CCK-8 method and flow cytometry.
After treatment with protease inhibitor MG132, the BCL6 protein level of K562/G01 significantly increased (P<0.05). The mRNA and protein expression level of ubiquitin-specific protease USP2 in K562/G01 cell line was higher than that in K562 cell line (P<0.05). After treatment of K562/G01 with USP2 protease inhibitor ML364, the expression levels of USP2 and BCL6 proteins were down-regulated simultaneously (P<0.05) . After combination of ML364 and IM, both the proliferation inhibitory rate and the apoptosis rate of K562/G01 cells significantly increased(P<0.05).
ML364 decreases the BCL6 protein stability in K562/G01 by inhibiting the USP2-mediated deubiquitination, and down-regulate the BCL6 protein experssion, thereby increases the sensitivity of drug-resistant cells to IM.
探讨泛素-蛋白酶体系统(UPS)对伊马替尼(IM)耐药的K562/G01细胞中BCL6蛋白水平、细胞增殖及凋亡的影响。
采用蛋白质免疫印迹法检测蛋白酶体抑制剂MG-132处理前后K562/G01细胞中BCL6的表达。分别采用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测泛素特异性蛋白酶USP2抑制剂ML364处理及未处理的K562/G01细胞中BCL6和USP2的mRNA及蛋白表达水平。采用细胞计数试剂盒-8(CCK-8)法和流式细胞术分析单独使用IM或联合ML364对K562/G01细胞增殖和凋亡的影响。
蛋白酶体抑制剂MG132处理后,K562/G01细胞中BCL6蛋白水平显著升高(P<0.05)。K562/G01细胞系中泛素特异性蛋白酶USP2的mRNA和蛋白表达水平高于K562细胞系(P<0.05)。用USP2蛋白酶体抑制剂ML364处理K562/G01后,USP2和BCL6蛋白表达水平同时下调(P<0.05)。ML364与IM联合使用后,K562/G01细胞的增殖抑制率和凋亡率均显著升高(P<0.05)。
ML364通过抑制USP2介导的去泛素化作用降低K562/G01细胞中BCL6蛋白的稳定性,下调BCL6蛋白表达,从而增加耐药细胞对IM的敏感性。