A voltage-activated Ca++ channel has been identified in the apical mem
branes of cultured rabbit proximal tubule cells using the patch-clamp
technique. With 105 mM CaCl2 solution in the pipette and 180 NaAsp in
the bath, the channel had a conductance of 10.4 +/- 1.0 pS (n = 8) in
on-cell patches, and 9.8 +/- 1.1 pS (n = 8) in inside-out patches. In
both on-cell and inside-out patches, the channel is active by membrane
depolarization. For this channel, the permeation to Ba++ and Ca++ is
highly selective over Na+ and K+ (P-Ca(Ba):P-Na(K) >200:1). The sensit
ivity to dihydropyridines is similar to that for L-type channels where
the channel was blocked by nifedipine (10 mu M), and activated by Bay
K 8644 (5 mu M). When activated by Bay K 8644, the channel showed sub
conductance levels. Treatment with forskolin (12.5 mu M), phorbol este
r (1 mu M), or stretching (40 cm water) did not activate this channel.
These results indicate that this Ca++ channel is mostly regulated by
membrane voltage, and appears to be an epithelial class of L-type Ca+ channel. As such, it may participate in calcium reabsorption during p
eriods of enhanced sodium reabsorption, or calcium signaling in volume
regulation, where membrane depolarization occurs for prolonged period
s.