Dual pools of actin at presynaptic terminals 1 2 3 4 5 6 7

We investigated actin's function in vesicle recycling and exocytosis at lamprey synapses, and show that FM1-43 puncta and phalloidin-labeled filamentous actin (F-actin) structures are colocalized, yet recycling vesicles are not contained within F-actin clusters. Additionally, phalloidin also labels a plasma membrane-associated cortical actin. Injection of fluorescent G-actin revealed activity-independent dynamic actin incorparation into presynaptic synaptic vesicle clusters but not into cortical actin. Latrunculin-A, which sequesters G-actin, dispersed vesicle associated actin structures and prevented subsequent labeled G-actin and phalloidin accumulation at presynaptic puncta, yet cortical phalloidin labeling persisted. Dispersal of presynaptic F-actin structures by Latrunculin-A did not disrupt vesicle clustering or recycling, nor alter the amplitude or kinetics of EPSCs. However, it slightly enhanced release during repetitive stimulation. While dispersal of presynaptic actin puncta using Latrunculin-A failed to disperse synaptic vesicles or inhibit synaptic transmission, presynaptic phalloidin injection blocked exocytosis and reduced endocytosis measured by action potential-evoked FM1-43 staining. Furthermore, phalloidin stabilization of only cortical actin following pretreatment with Latrunculin-A was sufficient to inhibit synaptic transmission. Conversely, treatement of axons with jasplakinolide, which induces F-actin accumulation but disrupts F-actin structures in vivo, resulted in increased synaptic transmission accompanied by a loss of phalloidin labeling of cortical actin but no loss of actin labeling within vesicle clusters. Marked synaptic deficits seen with phalloidin stabilization of cortical F-actin, in contrast to the minimal effects of disruption of a synaptic vesicle associated F-actin, led us to conclude that two structurally and functionally distinct pools of actin exist at presynaptic sites.