Permissive Modulation of Sphingosine-1-Phosphate-Enhanced Intracellular Calcium on BK Channel of Chromaffin Cells.

Sphingosine-1-phosphate (S1P), is a signaling sphingolipid which acts as a bioactive lipid mediator. We assessed whether S1P had multiplex effects in regulating the large-conductance Ca-activated K channel (BK) in catecholamine-secreting chromaffin cells. Using multiple patch-clamp modes, Ca imaging, and computational modeling, we evaluated the effects of S1P on the Ca-activated K currents () in bovine adrenal chromaffin cells and in a pheochromocytoma cell line (PC12). In outside-out patches, the open probability of BK channel was reduced with a mean-closed time increment, but without a conductance change in response to a low-concentration S1P (1 µM). The intracellular Ca concentration (Ca) was elevated in response to a high-dose (10 µM) but not low-dose of S1P. The single-channel activity of BK was also enhanced by S1P (10 µM) in the cell-attached recording of chromaffin cells. In the whole-cell voltage-clamp, a low-dose S1P (1 µM) suppressed , whereas a high-dose S1P (10 µM) produced a biphasic response in the amplitude of , i.e., an initial decrease followed by a sustained increase. The S1P-induced enhancement was abolished by BAPTA. Current-clamp studies showed that S1P (1 µM) increased the action potential (AP) firing. Simulation data revealed that the decreased BK conductance leads to increased AP firings in a modeling chromaffin cell. Over a similar dosage range, S1P (1 µM) inhibited and the permissive role of S1P on the BK activity was also effectively observed in the PC12 cell system. The S1P-mediated stimulation may result from the elevated Ca, whereas the inhibition of BK activity by S1P appears to be direct. By the differentiated tailoring BK channel function, S1P can modulate stimulus-secretion coupling in chromaffin cells.