La. Fieber et Mc. Schmale, DIFFERENCES IN A K-CURRENT IN SCHWANN-CELLS FROM NORMAL AND NEUROFIBROMATOSIS-INFECTED DAMSELFISH, Glia, 11(1), 1994, pp. 64-72
Patch clamp techniques were used to study whole cell ionic currents in
Schwann cells (SC) from a tropical marine fish, the bicolor damselfis
h, Pomacentrus partitus. The bicolor damselfish is affected by a disea
se termed damselfish neurofibromatosis (DNF), being developed as an an
imal model of neurofibromatosis-type 1 (NF1) in humans. NF1 affects SC
, fibroblasts, and perineurial cells. The sole depolarization-activate
d ionic current present in cultured SC from normal fish peripheral ner
ve and from neurofibromas of fish with induced or spontaneously occurr
ing DNF was an inactivating K+ current (K current), with a strong depe
ndence on the Nernst potential for K+ This K current activated at depo
larizations to -40 mV and above and inactivated during a maintained te
st pulse (0.2-1 s), but inactivation was significantly greater in tumo
red SC. Both currents were inhibited by 4-aminopyridine (K-d similar t
o 1 mM) and by dendrotoxin (15 mu M) but were insensitive to extracell
ular tetraethyammonium (less than or equal to 150 mM), indicating that
the whole cell currents were similar pharmacologically. The currents
could be distinguished on the basis of their sensitivity to depolarize
d holding potential, with normal cells less sensitive. Half-inactivati
on of the current was -32 mV in normal cells and -38 mV in tumored cel
ls. Inactivation curves constructed from the average normalized curren
t for many SC were significantly different in normal and tumored cells
. When the depolarized holding potential was maintained between test d
epolarizations, greater voltage-dependent inactivation in tumored cell
s was apparent. Normal cells maintained an average of 36% of peak curr
ent at a holding voltage of -40 mV, while in tumored cells this averag
e was 12%, a significant difference. (C) 1994 Wiley-Liss, Inc.