A PEG-containing surface coating was investigated as a means to control neu
rite outgrowth in the presence of serum. Various ratios of end-group-activa
ted triblock copolymer Pluronic(TM) F108 were used to immobilize the extrac
ellular matrix protein fibronectin (FN). Primary cultures of dorsal root ga
nglion neurons were cultured on F108-immobilized FN or, as a control, on FN
adsorbed from solution directly to polystyrene. Although FN surface concen
tration could be controlled in a dose-dependent manner by either technique,
dose-dependent control of neuronal behaviors was best achieved on F108-imm
obilized FN. This effect was similar regardless of the presence of serum in
the culture medium. F108-immobilized FN supported twofold greater maximal
neurite outgrowth than did directly adsorbed FN. Furthermore, at similar su
rface concentrations, F108-FN was significantly more active in promoting ne
urite outgrowth. Polypropylene filament bundles treated with F108-immobiliz
ed FN supported robust outgrowth from explants of dorsal root ganglia, demo
nstrating the utility of the surface coating on clinically relevant materia
ls with more complex shapes. The ability to control neuronal behaviors in a
serum-resistant manner, coupled with enhanced biologic activity, demonstra
tes the potential for surfactant-based immobilization as a method for gener
ating biointeractive materials for tissue engineering. (C) 2000 John Wiley
& Sons, Inc.