Using a noninvasive vibrating electrode for the measurement of extrace
llular current, we show that a polarized ionic current traverses the e
mbryo for many hours in the anuran, perhaps days in the urodele follow
ing gastrulation. The voltage driving these ionic currents is an inter
nally positive transepithelial potential (TEP) normally expressed acro
ss embryonic integuments. Current is driven out of the lateral walls o
f the neural folds and the blastopore and enters most of the rest of t
he embryo's body surface. The magnitude of the TEP is transitorily dep
endent on external sodium and can be reduced by the embryo's immersion
in Na+ depleted media or by treatment with 50 mu M amiloride. Both tr
eatments fail to chronically reduce externally detected currents, howe
ver. The pattern of currents traversing the embryo suggests they would
be associated with rostral-caudal and medial-lateral gradients of vol
tage within the embryo. By sampling the distribution of TEPs in axolot
l embryos, we provide measurements of the former-an internal, caudally
negative, potential gradient beneath the neural plate ectoderm. The m
agnitude of these endogenous fields is on the order of 10 to 20 mV/mm
and is within a range of potential known to affect the shape and migra
tion of a variety of embryonic cell types in vitro. We suggest that en
dogenous currents and voltages in the vertebrate embryo may provide gr
oss cues for cell movement and emerging developmental pattern. (C) 199
4 Wiley-Liss, Inc.