Liu H S, Jan M S, Chou C K, Chen P H, Ke N J
Medical College, National Cheng Kung University, Tainan, Taiwan, Republic of China.
Biochem Biophys Res Commun. 1999 Jul 14;260(3):712-7. doi: 10.1006/bbrc.1999.0954.
Green fluorescent protein (GFP) has become more popular to be used as a living marker for positively transfected clones in many studies. To establish stable cell lines constitutively expressing GFP, three GFPs expressed from plasmid pBIEGFP, pSG5GFP, and pRSGFP were introduced into NIH/3T3, BHK-21, Huh-7, and HepG2 cells. All the GFPs we used are the mutant forms of a common wild phenotype. The pBIEGFP expressed enhanced GFP (EGFP). The pRSGFP and pSG5GFP expressed red shift GFP (RSGFP). The RSGFP gene in pSG5GFP was driven by a strong SV40 promoter and showed at least 20-fold higher RSGFP expression by western blot analysis. Despite of the variation in the levels of GFP expression, many GFP expressing cells contracted, rounded-up, and died, which was confirmed by decreasing luciferase activity. CPP32 activity and flow cytometric analyses further demonstrate that cells expressing GFP underwent apoptosis. Our observation is contradictory to other reports that GFP is nontoxic to the cells. Most importantly, this paper shows for the first time the link between expression of GFP and induction of apoptosis. This finding should promote studies of GFP cytotoxicity and attempts to isolate new non-toxic mutants of GFP.
在许多研究中,绿色荧光蛋白(GFP)作为阳性转染克隆的活体标记物越来越受欢迎。为了建立稳定表达GFP的细胞系,将从质粒pBIEGFP、pSG5GFP和pRSGFP表达的三种GFP导入NIH/3T3、BHK-21、Huh-7和HepG2细胞。我们使用的所有GFP都是常见野生型的突变形式。pBIEGFP表达增强型GFP(EGFP)。pRSGFP和pSG5GFP表达红移GFP(RSGFP)。pSG5GFP中的RSGFP基因由强SV40启动子驱动,蛋白质免疫印迹分析显示其RSGFP表达至少高20倍。尽管GFP表达水平存在差异,但许多表达GFP的细胞收缩、变圆并死亡,荧光素酶活性降低证实了这一点。CPP32活性和流式细胞术分析进一步表明,表达GFP的细胞发生了凋亡。我们的观察结果与其他关于GFP对细胞无毒的报道相矛盾。最重要的是,本文首次展示了GFP表达与凋亡诱导之间的联系。这一发现应促进对GFP细胞毒性的研究,并推动分离新的无毒GFP突变体的尝试。