Doc2 Is a Ca2+ Sensor Required for Asynchronous Neurotransmitter Release

SummarySynaptic transmission involves a fast synchronous phase and a slower asynchronous phase of neurotransmitter release that are regulated by distinct Ca2+ sensors. Though the Ca2+ sensor for rapid exocytosis, synaptotagmin I, has been studied in depth, the sensor for asynchronous release remains unknown. In a screen for neuronal Ca2+ sensors that respond to changes in [Ca2+] with markedly slower kinetics than synaptotagmin I, we observed that Doc2—another Ca2+, SNARE, and lipid-binding protein—operates on timescales consistent with asynchronous release. Moreover, up- and downregulation of Doc2 expression levels in hippocampal neurons increased or decreased, respectively, the slow phase of synaptic transmission. Synchronous release, when triggered by single action potentials, was unaffected by manipulation of Doc2 but was enhanced during repetitive stimulation in Doc2 knockdown neurons, potentially due to greater vesicle availability. In summary, we propose that Doc2 is a Ca2+ sensor that is kinetically tuned to regulate asynchronous neurotransmitter release.

Graphical AbstractFigure optionsDownload high-quality image (224 K)Download as PowerPoint slideHighlights
► Doc2 responds to changes in [Ca2+] with slower kinetics than synaptotagmin I
► Doc2 specifically modulates the asynchronous phase of neurotransmitter release
► Changes in Doc2 levels indirectly affect synchronous release
► Doc2 is required for persistent reverberation in a neural network