Na-K-2Cl Cotransporter and Store-Operated Ca(2+) Entry in Pacemaking by Interstitial Cells of Cajal.

Pacemaker depolarization in interstitial cells of Cajal (ICCs) is believed to be induced by Ca(2+) transients and activation of anoctamin-1 (Ano1) channels in the plasma membrane. However, block of store-operated calcium entry (SOCE) or the Na-K-2Cl cotransporter (NKCC1) terminates pacemaker activity in ICC, indicating these transporters are involved in the initiation or maintenance of pacemaker activity. We hypothesized that SOCE contributes to pacemaker depolarization by maintaining [Ca(2+)] in the endoplasmic reticulum, which is the underlying source of Ca(2+) transients for activation of Ano1. NKCC1 maintains the Cl(-) gradient supporting the driving force for inward current mediated by Ano1. Currently mechanisms sustaining release of Ca(2+) and activation of Ano1 channels during the plateau phase of slow waves are unknown, but the reverse mode of the Na(+)/Ca(2+) exchange may contribute. We generated a mathematical model of pacemaker activity based on current empirical observations from ICC of mouse small intestine that incorporates functions of SOCE and NKCC1. This model reproduces experimental findings, suggesting roles for SOCE and Ano1 channels: blocking of either NKCC1 or SOCE in our model terminates pacemaker activity. Direct contribution of NKCC1 to pacemaker activity in a beat-to-beat manner is not predicted by our model. Instead, NKCC1 plays a maintenance role supporting the driving force for Cl(-) efflux. Incorporation of SOCE allows the model to drive pacemaker activity without a diastolic depolarization, as observed in cardiac pacemaking. Further biological experiments are necessary to validate and further refine the roles of NKCC1, Na(+)/Ca(2+) exchange, and Ano1 in the pacemaker mechanism of ICC.