Abe Shinya, Hasegawa Maki, Yamamoto Kouhei, Kurata Morito, Nakagawa Yasunori, Suzuki Kenshi, Takizawa Touichiro, Kitagawa Masanobu
Department of Comprehensive Pathology, Aging and Developmental Sciences, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.
Exp Mol Pathol. 2007 Dec;83(3):405-12. doi: 10.1016/j.yexmp.2007.04.001. Epub 2007 Apr 18.
We studied the expression dynamics of inhibitor of apoptosis protein (IAP) family members and Smac/DIABLO after treatment with doxorubicin in human multiple myeloma cell line RPMI 8226 and its doxorubicin-resistant variant DRR. Proapoptotic stimulation with doxorubicin rapidly induced the overexpression of mRNA as well as protein for IAPs in RPMI 8226 cells followed by a gradual decrease of their expression. Smac/DIABLO, which is known to neutralize IAPs, showed increased expression at the mRNA level after treatment; however, Western blot analysis revealed a slight decrease of the amount of protein. Immunoprecipitation analysis revealed the association of Smac/DIABLO with cIAP1 or XIAP after treatment with doxorubicin. In contrast to the RPMI 8226 cells, DRR cells did not undergo apoptosis in response to doxorubicin treatment. The DRR cells had higher levels of IAPs expression at the mRNA level and did not show a remarkable peak or decrease in the expression of mRNAs for cIAP1, cIAP2, XIAP, and survivin after treatment with doxorubicin. Furthermore, the expression of Smac/DIABLO mRNA was not up-regulated after treatment. These findings indicate that the suppression of IAPs expression by Smac/DIABLO shortly after proapoptotic stimulation might play a role in the mechanisms of apoptotic induction, and that the maintenance of high IAPs expression and low Smac/DIABLO expression after treatment might lead to the doxorubicin-resistance of multiple myeloma cells.
我们研究了阿霉素处理后人多发性骨髓瘤细胞系RPMI 8226及其阿霉素耐药变体DRR中凋亡抑制蛋白(IAP)家族成员和Smac/DIABLO的表达动态。阿霉素的促凋亡刺激迅速诱导RPMI 8226细胞中IAPs的mRNA和蛋白过表达,随后其表达逐渐下降。已知可中和IAPs的Smac/DIABLO在处理后mRNA水平表达增加;然而,蛋白质印迹分析显示蛋白质含量略有下降。免疫沉淀分析显示阿霉素处理后Smac/DIABLO与cIAP1或XIAP相关。与RPMI 8226细胞相反,DRR细胞对阿霉素处理不发生凋亡。DRR细胞在mRNA水平上IAPs表达水平较高,在用阿霉素处理后,cIAP1、cIAP2、XIAP和survivin的mRNA表达未显示出明显的峰值或下降。此外,处理后Smac/DIABLO mRNA的表达未上调。这些发现表明,促凋亡刺激后不久Smac/DIABLO对IAPs表达的抑制可能在凋亡诱导机制中起作用,并且处理后IAPs高表达和Smac/DIABLO低表达的维持可能导致多发性骨髓瘤细胞对阿霉素耐药。