Pm. Verbost et al., BRANCHIAL CALCIUM-UPTAKE - POSSIBLE MECHANISMS OF CONTROL BY STANNIOCALCIN, Fish physiology and biochemistry, 11(1-6), 1993, pp. 205-215
The branchial Ca2+ uptake by teleost fish is under inhibitory control
by the hormone stanniocalcine (STC) which is generated by the corpuscl
es of Stannius (CS). Removal of the CS in North American eel, Anguilla
rostrata LeSueur, induced a rapid rise in blood calcium levels. Branc
hial Ca2+ influx following the extirpation of the CS (stanniectomy, ST
X) increased during the first four days and stayed elevated thereafter
(in agreement with previous studies). The transepithelial potential (
TEP) across the gills did not change after STX and this means that the
electrochemical gradient for Ca2+ is less favourable for passive infl
ux of Ca2+ in STX eel. Therefore, the Call influx in STX eels is a tra
nscellular flux, with Ca2+ crossing the apical and basolateral membran
e barrier. The kinetics of ATP-driven Ca2+-transport across basolatera
l plasma membranes from eel gills did not change after STX. Thus, the
increased Ca2+-influx after STX is not correlated with changes in ATP-
dependent Ca2+-extrusion across the basolateral membrane, suggesting a
regulation at the apical membrane. Moreover, STC did not affect ATP-d
riven Ca2+-transport in isolated basolateral membranes (in vitro). STC
(0.1 nM) reduced cAMP levels in dispersed eel gill cells. It had no s
ignificant effect on the IP3 levels in these cells. We postulate that
STC controls the permeability to Ca2+ of the apical membranes of the C
a2 + transporting cells of fish gills by controlling second messenger
operated Ca2+ channels in the apical membrane.