| Literature DB >> 31383765 |
Dinara Bulgari1, David L Deitcher2, Brigitte F Schmidt3, M Alexandra Carpenter4, Christopher Szent-Gyorgyi3, Marcel P Bruchez3,4,5, Edwin S Levitan6.
Abstract
Synaptic release of neuropeptides packaged in dense-core vesicles (DCVs) regulates synapses, circuits, and behaviors including feeding, sleeping, and pain perception. Here, synaptic DCV fusion pore openings are imaged without interference from cotransmitting small synaptic vesicles (SSVs) with the use of a fluorogen-activating protein (FAP). Activity-evoked kiss and run exocytosis opens synaptic DCV fusion pores away from active zones that readily conduct molecules larger than most native neuropeptides (i.e., molecular weight [MW] up to, at least, 4.5 kDa). Remarkably, these synaptic fusion pores also open spontaneously in the absence of stimulation and extracellular Ca2+ SNARE perturbations demonstrate different mechanisms for activity-evoked and spontaneous fusion pore openings with the latter sharing features of spontaneous small molecule transmitter release by active zone-associated SSVs. Fusion pore opening at resting synapses provides a mechanism for activity-independent peptidergic transmission.Entities:
Keywords: Drosophila; fusion pore; neuromuscular junction; neuropeptide release; secretory granule
Year: 2019 PMID: 31383765 PMCID: PMC6708360 DOI: 10.1073/pnas.1905322116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205