Gopinath P, Ghosh Siddhartha Sankar
Department of Biotechnology, Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati, 781039, India.
Mol Cell Biochem. 2009 Apr;324(1-2):21-9. doi: 10.1007/s11010-008-9980-5. Epub 2008 Dec 14.
Cytosine deaminase-uracil phosphoribosyl transferase (CD-UPRT) fusion gene is known to exhibit therapeutic effect by inducing apoptosis in vitro. However, bystander effects of 5-flurocytosine (5-FC)/CD-UPRT and the molecular mechanism for apoptosis are yet to be established. In the present study, we have generated BHK21 cell line expressing both CD-UPRT and green fluorescent protein (GFP) from two separate transcripts, where GFP was used as a noninvasive probe to monitor the therapeutic effect of CD-UPRT. Enzyme activity of CD-UPRT in the stable cell line was measured by the reverse phase high-performance liquid chromatography analysis. Inhibition of cell growth and strong bystander effects of 5-FC/CD-UPRT were established, whereas characteristic surface morphology of apoptotic cell death was identified by AFM analysis. Involvement of various apoptotic signaling genes using semi-quantitative RT-PCR has been explored to substantiate the potential application of 5-FC/CD-UPRT suicide gene in therapy.
已知胞嘧啶脱氨酶-尿嘧啶磷酸核糖转移酶(CD-UPRT)融合基因在体外可通过诱导细胞凋亡发挥治疗作用。然而,5-氟胞嘧啶(5-FC)/CD-UPRT的旁观者效应以及细胞凋亡的分子机制尚未明确。在本研究中,我们从两个独立转录本构建了同时表达CD-UPRT和绿色荧光蛋白(GFP)的BHK21细胞系,其中GFP用作无创探针以监测CD-UPRT的治疗效果。通过反相高效液相色谱分析测定稳定细胞系中CD-UPRT的酶活性。确定了5-FC/CD-UPRT对细胞生长的抑制作用和强烈的旁观者效应,而通过原子力显微镜分析鉴定了凋亡细胞死亡的特征性表面形态。已利用半定量逆转录-聚合酶链反应探索各种凋亡信号基因的参与情况,以证实5-FC/CD-UPRT自杀基因在治疗中的潜在应用。