Green fluorescent protein (GFP) has become more popular to be used as a liv
ing 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 comm
on wild phenotype. The pBIEGFP expressed enhanced GFP (EG;FP). The pRSGFP a
nd pSG5GFP expressed redshift GFP (RSGFP). The RSGFP gene in pSG5GFP was dr
iven by a strong SV40 promoter and showed at least 20-fold higher RSGFP exp
ression 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 unde
rwent 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 f
inding should promote studies of GFP cytotoxicity and attempts to isolate n
ew non-toxic mutants of GFP. (C) 1999 Academic Press.