Schematic models of possible mechanisms by which K+ channels could control cell migration and proliferation processes. A: changes in membrane potential (ΔVm), cell volume/shape, pH (ΔpH), Ca2+ signal {intracellular Ca2+ concentration ([Ca2+]in)}, or other signaling pathways could trigger the effect of K+ channel modulation on cell migration/proliferation. B: bidirectional autocrine loop linking K+ channels to growth factor receptors, such EGFR, may be another control mechanism of epithelial repair by K+ channels. C: direct interaction between K+ channels and proteins of the migratory machinery such as integrins and cytoskeleton may also occur during wound repair.