Immobilized cultured tobacco cells become polarized upon the addition of na
phthalene-1-acetic acid and start to elongate from an initial spherical sha
pe. The question as to how a diffuse-growing cell forms a polar axis is add
ressed here with approaches successfully applied to the study of tip growth
. With two kinds of vibrating probes the electric current flow and proton f
luxes were mapped around such elongating cells. No consistent polar pattern
of ion fluxes, which is typical for actively tip-growing cells, was detect
ed. Therefore, other signals must provide the positional information needed
for polar axis formation. Furthermore, neither a specific pattern of intra
cellular Ca2+ concentration nor a polar distribution of putative ion-channe
l antagonist-binding sites were found in elongating tobacco cells. Auxin fl
ux, on the other hand, was found to be important as TIBA, an inhibitor of p
olar auxin transport, clearly inhibited elongation in a concentration-depen
dent way. Cross-linking of arabinogalactan-proteins with the beta -Yariv re
agent also resulted in inhibition of elongation. A model is proposed for th
e induction of polar growth where localized auxin efflux starts a signal ca
scade that triggers molecules that reorient microtubules. These then guide
cellulose deposition in the cell wall, which in turn alters cell wall mecha
nics and leads to elongation. In this scheme, arabinogalactan-proteins are
not causal agents but are probably important regulators of growth and survi
val of the cell.