Fibroblast growth factors (FGF) are expressed at high levels in the ce
ntral nervous system (CNS), however their function in the CNS is not w
ell understood. The immortalized neuronal cell line (BK1), derived fro
m a transgenic mouse central nervous system tumor, expresses high leve
ls of FGF receptor 1 (FGFR1) and demonstrates both morphologic and bio
chemical changes when treated with basic FGF (FGF-2). We have derived
subclones of BK1 cells with varying degrees of FGF responsiveness by t
ransfecting either a wild type (FRW) or a truncated (FRX) form of FGFR
1. Cells expressing high levels of FGFR1 rapidly and uniformly respond
to FGF, while cells expressing FRX fail to respond to FGF, either mor
phologically or by the expression of molecular markers. These BK1 subc
lones will prove useful to study FGFR mediated signal transduction and
FGFR responsive genes in a Ch'S derived cell. These studies also demo
nstrate that a dominant negative FGF receptor can be used as a tool to
elucidate the function of FGF in the central nervous system.