Differential properties of GTP- and Ca2+-Stimulated exocytosis from large dense core vesicles

Many cells utilize a GTP-dependent pathway to trigger exocytosis in addition to Ca2+-triggered exocytosis. However, little is known about the mechanism by which GTP triggers exocytosis independent of Ca2+. We used dual-color evanescent field microscopy to compare the motion and fusion of large dense core vesicles stimulated by either mastoparan (Mas) in Ca2+-free conditions or high K+ in the presence of Ca2+. We demonstrate that Mas is hardly effective in triggering the fusion of the predocked vesicles but predominantly mobilizes cytosolic vesicles. In contrast, Ca2+-dependent exocytosis is largely due to predocked vesicles. Fusion kinetics analysis and carbon-fiber amperometry reveal that Mas induces a brief 'kiss-and-run' fusion and releases only a small amount of the cargo, whereas Ca2+ stimulates a more persistent opening of the fusion pore and larger release of the contents. Furthermore, we show that Mas-released vesicles require a much shorter time to reach fusion competence once they approach the plasma membrane. Our data suggest the involvement of different mechanisms not only in triggering and fusion but also in the docking and priming process for Ca2+- and GTP-dependent exocytosis.