In this study, we have used spatially defined surfaces of organic thin
films to micropattern the outgrowth of central nervous system neurons
in culture. Glass substrates were first chemically modified with synt
hetic peptides derived from an extra-cellular matrix protein laminin t
o couple a functionality that promotes a neuron-substrate interaction.
The modification procedure was verified using X-ray photoelectron spe
ctroscopy, The functionality of the modified glass surfaces was examin
ed by growing neurons dissociated from mammalian central nervous tissu
es in culture, Spatially defined surfaces of the peptide were then fab
ricated by selectively attaching the peptide to coplanar surfaces that
were produced via deep UV laser lithography of self-assembled monolay
er films. The interaction of the neurons and substrates confined the a
ttachment of cell bodies on the defined surfaces and allowed the exten
sion of neuritic processes along the defined pathways, Atomic force mi
croscopy revealed fine structures of the patterned neurons and enabled
us to directly observe the substratum-guided neuronal outgrowth. (C)
1997 Elsevier Science S.A.