Is green fluorescent protein toxic to the living cells?

被引:453
作者
Liu, HS [1 ]
Jan, MS [1 ]
Chou, CK [1 ]
Chen, PH [1 ]
Ke, NJ [1 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Microbiol & Immunol, Tainan 70101, Taiwan
关键词
GFP; luciferase analysis; living cell marker; apoptosis;
D O I
10.1006/bbrc.1999.0954
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (EG;FP). The pRSGFP and pSG5GFP expressed redshift 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 how 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. (C) 1999 Academic Press.
引用
收藏
页码:712 / 717
页数:6
相关论文
共 15 条
  • [1] EGFP-containing vector system that facilitates stable and transient expression assays
    Alexander, L
    Lee, H
    Rosenzweig, M
    Jung, JU
    Desrosiers, RC
    [J]. BIOTECHNIQUES, 1997, 23 (01) : 64 - 66
  • [2] CELL-DEATH IN HEALTH AND DISEASE - THE BIOLOGY AND REGULATION OF APOPTOSIS
    BELLAMY, COC
    MALCOMSON, RDG
    HARRISON, DJ
    WYLLIE, AH
    [J]. SEMINARS IN CANCER BIOLOGY, 1995, 6 (01) : 3 - 16
  • [3] RENATURATION OF AEQUOREA GREEN-FLUORESCENT PROTEIN
    BOKMAN, SH
    WARD, WW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 101 (04) : 1372 - 1380
  • [4] Simplification of titer determination for recombinant baculovirus by green fluorescent protein marker
    Cha, HJ
    Gotoh, T
    Bentley, WE
    [J]. BIOTECHNIQUES, 1997, 23 (05) : 782 - &
  • [5] GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION
    CHALFIE, M
    TU, Y
    EUSKIRCHEN, G
    WARD, WW
    PRASHER, DC
    [J]. SCIENCE, 1994, 263 (5148) : 802 - 805
  • [6] Pest control by fluorescence
    Chao, YC
    Chen, SL
    Li, CF
    [J]. NATURE, 1996, 380 (6573) : 396 - 397
  • [7] *CLONT, 1997, AP CPP32 ASS KITS
  • [8] *CLONT, 1996, LIV COL GFP APPL NOT
  • [9] CHEMICAL-STRUCTURE OF THE HEXAPEPTIDE CHROMOPHORE OF THE AEQUOREA GREEN-FLUORESCENT PROTEIN
    CODY, CW
    PRASHER, DC
    WESTLER, WM
    PRENDERGAST, FG
    WARD, WW
    [J]. BIOCHEMISTRY, 1993, 32 (05) : 1212 - 1218
  • [10] Applications of green fluorescent protein in plants
    Leffel, SM
    Mabon, SA
    Stewart, CN
    [J]. BIOTECHNIQUES, 1997, 23 (05) : 912 - +