LANTHANUM CAN BE TRANSPORTED BY THE SODIUM-CALCIUM EXCHANGE PATHWAY AND DIRECTLY TRIGGERS CATECHOLAMINE RELEASE FROM BOVINE CHROMAFFIN CELLS

A comparison of the effectiveness of the trivalent cation, lanthanum ( La3+) relative to Ca2+ in causing catecholamine release from bovine ch romaffin cells has been made, together with a determination of the pat hway by which La3+ enters these cells. In chromaffin cells maintained in tissue culture and permeabilised with digitonin, both La3+ and Ca2 caused H-3 release from cells preloaded with [H-3]-noradrenaline; La3 + and Ca2+ caused similar maximal release but the EC(50) for La3+ was an order of magnitude less than that for Ca2+. At maximal release caus ed by either La3+ or Ca2+ (approximately 14% of cell H-3 content in 15 min), the other cation caused a small, but significant, further relea se. At submaximal effective concentrations the effects of the two cati ons were exactly additive. Using H-3 release as an indicator of cytoso lic La3+, its route of entry into intact chromaffin cells was investig ated. With La3+-containing medium there was no release evoked by nicot ine or by K+-depolarisation indicating that La3+ does not enter either via the nicotinic receptor linked ion channel or via voltage-sensitiv e (Ca2+) channels. However, in sodium-loaded chromaffin cells (ouabain incubation in Ca2+-free medium for 15 min) exposore to bating media c ontaining either Ca2+ or La3+ caused H-3 release. La3+ (0.1 mM) caused a release similar in magnitude to that caused by Ca2+ (about 1 mM). L a3+ at low concentrations had an additive (0.1 mM La3+) or synergistic (0.25-0.45 mM La3+) action with Ca2+ (< 3.6 mM) on H-3 release. At hi gher concentrations (> 0.9 mM) the effects of La3+ predominated and pr evented the expected effects of Ca2+ In other experiments, La3+ (1 mM) blocked export of Ca-45(2+) via both Na-o-dependent and independent p athways, i.e. sodium-calcium exchange and the calcium pump. The result s indicate that La3+ can enter bovine chromaffin cells via the Na-i/C- ao exchange pathway independently of, or together with, Ca2+ but, that concentrations above 0.9 mM block the influx or efflux of Ca2+. Howev er, Ca2+, even at 3.6 mM, did not block the influx of La3+. The result s further indicate that, within chromaffin cells, La3+ is at least as effective as Ca2+ in triggering catecholamine release and maintaining prolonged release. La3+ also appears to act cooperatively with Ca2+ at the release pathway.