Cell migration plays a central role in many physiological and pathophysiological processes. On a cellular level it is based on a highly coordinated restructuring of the cytoskeleton, a continuous cycle of adhesion and de-adhesion as well as on the activity of ion channels and transporters. The cytoplasmic Ca ²⁺ ([Ca ²⁺ ] _i ) concentration is an important coordinator of these intracellular processes. Thus, [Ca ²⁺ ] _i must be tightly controlled in migrating cells. This is among other things achieved by the activity of Ca ²⁺ permeable channels, the plasma membrane Ca ²⁺ -ATPase (PMCA) and the Na ⁺ /Ca ²⁺ exchanger (NCX) in the plasma membrane. Here, we wanted to determine the functional role of these transport proteins in cell migration. We therefore quantified the acute effect of inhibitors of these transport proteins (Gd ³⁺ , vanadate, KB-R7943) on migration, [Ca ²⁺ ] _i , and intracellular pH (pH _i ) of MDCK-F cells. Migration was monitored with computer-assisted time-lapse video microscopy. [Ca ²⁺ ] _i and pH _i . were measured with the fluorescent indicators fura-2 and BCECF. NCX expression in MDCK-F cells was verified with ion substitution experiments, and expression of PMCA was tested with RT-PCR. All blockers lead to a rapid impairment of cell migration. However, the most prominent effect is elicited by NCX-inhibition with KB-R7943. NCX-blockade leads to an almost complete inhibition of migration which is accompanied by a dose-dependent increase of [Ca ²⁺ ] _i and an intracellular alkalinisation. We show that inhibition of NCX and PMCA strongly affects lamellipodial dynamics of migrating MDCK-F cells. Taken together, our results show that PMCA and in particular NCX are of critical importance for cell migration.