Ascidian tadpole larvae, composed of only about 2500 cells, have a pri
mitive nervous system which is derived from the neural plate. The ster
eotyped cell cleavage pattern and well characterized cell lineage in t
hese animals allow the isolation and culture of identified blastomeres
in variable combinations. Ascidian embryos express cell-type-specific
markers corresponding to their cell fates, even when cultured under c
leavage-arrest by cytochalasin B. This system provides us with a uniqu
e opportunity to study the roles of cell lineage and cell contact in e
arly neuronal differentiation in the absence of events associated with
complex morphogenesis. In addition, the isolated, cleavage-arrested b
lastomeres are ideally suited to electrical recording, permitting the
use of ionic channels as specific markers for differentiation. In the
cleavage-arrested embryos, suppression of one type of K+ channel, and
induction of two types of Na+ channels, occur following cell contact w
ith the vegetal blastomere. The combination of molecular and electroph
ysiological analyses on this simple animal system may provide insights
into the nature of the cell interactions important in early neurogene
sis, both in ascidians and in vertebrates.