Shirasaka Yoshiyuki, Konishi Reiko, Funami Nana, Kadowaki Yuko, Nagai Yuri, Sakaeda Toshiyuki, Yamashita Shinji
Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, Japan.
Biopharm Drug Dispos. 2009 Apr;30(3):149-52. doi: 10.1002/bdd.650.
The purpose of this study was to investigate the correlation between mRNA and protein levels for P-glycoprotein (P-gp) expressed in various cell lines to validate the estimation of P-gp activity from its mRNA levels. P-gp expression levels in various cell monolayers, normal, P-gp-induced, P-gp-highly induced, (multidrug resistance, MDR) MDR1-knockdown (A2-2) and MDR1-knockdown (B2-2) Caco-2 cells and MDCKII/MDR1 cells, were quantified by real-time quantitative polymerase chain reaction (PCR) and western blot analysis. Both mRNA and protein levels of P-gp were lowest in the MDR1-knockdown (B2-2) Caco-2 cells, followed by the MDR1-knockdown (A2-2) Caco-2, normal Caco-2, P-gp-induced Caco-2 and P-gp-highly induced Caco-2 cells, and highest in the MDCKII/MDR1 cells. Except for the MDCKII/MDR1 cells, the protein levels of P-gp in all Caco-2 cell lines showed a linear correlation with its mRNA levels; however, although the MDR1 mRNA level in MDCKII/MDR1 cells was much higher than in the P-gp-highly induced Caco-2 cells, the protein levels were almost the same in both cells. From these findings, it was suggested that P-gp activity in MDCKII/MDR1 cells could not be estimated from its mRNA levels.
本研究的目的是调查多种细胞系中表达的P-糖蛋白(P-gp)的mRNA水平与蛋白质水平之间的相关性,以验证根据其mRNA水平估算P-gp活性的方法。通过实时定量聚合酶链反应(PCR)和蛋白质印迹分析对多种细胞单层(正常、P-gp诱导、P-gp高度诱导、多药耐药(MDR)的MDR1基因敲低(A2-2)和MDR1基因敲低(B2-2)的Caco-2细胞以及MDCKII/MDR1细胞)中的P-gp表达水平进行定量。P-gp的mRNA和蛋白质水平在MDR1基因敲低(B2-2)的Caco-2细胞中最低,其次是MDR1基因敲低(A2-2)的Caco-2细胞、正常Caco-2细胞、P-gp诱导的Caco-2细胞和P-gp高度诱导的Caco-2细胞,在MDCKII/MDR1细胞中最高。除MDCKII/MDR1细胞外,所有Caco-2细胞系中P-gp的蛋白质水平与其mRNA水平呈线性相关;然而,尽管MDCKII/MDR1细胞中的MDR1 mRNA水平远高于P-gp高度诱导的Caco-2细胞,但两种细胞中的蛋白质水平几乎相同。从这些发现表明,无法根据MDCKII/MDR1细胞中的mRNA水平估算其P-gp活性。