| Literature DB >> 28718765 |
Shin-Ya Takemura1, Yoshinori Aso1, Toshihide Hige1, Allan Wong1, Zhiyuan Lu1, C Shan Xu1, Patricia K Rivlin1, Harald Hess1, Ting Zhao1, Toufiq Parag1, Stuart Berg1, Gary Huang1, William Katz1, Donald J Olbris1, Stephen Plaza1, Lowell Umayam1, Roxanne Aniceto1, Lei-Ann Chang1, Shirley Lauchie1, Omotara Ogundeyi1, Christopher Ordish1, Aya Shinomiya1, Christopher Sigmund1, Satoko Takemura1, Julie Tran1, Glenn C Turner1, Gerald M Rubin1, Louis K Scheffer1.
Abstract
Understanding memory formation, storage and retrieval requires knowledge of the underlying neuronal circuits. In Drosophila, the mushroom body (MB) is the major site of associative learning. We reconstructed the morphologies and synaptic connections of all 983 neurons within the three functional units, or compartments, that compose the adult MB's α lobe, using a dataset of isotropic 8 nm voxels collected by focused ion-beam milling scanning electron microscopy. We found that Kenyon cells (KCs), whose sparse activity encodes sensory information, each make multiple en passant synapses to MB output neurons (MBONs) in each compartment. Some MBONs have inputs from all KCs, while others differentially sample sensory modalities. Only 6% of KC>MBON synapses receive a direct synapse from a dopaminergic neuron (DAN). We identified two unanticipated classes of synapses, KC>DAN and DAN>MBON. DAN activation produces a slow depolarization of the MBON in these DAN>MBON synapses and can weaken memory recall.Entities:
Keywords: D. melanogaster; EM reconstruction; dopaminergic neuron; memory recall; mushroom body; neuroscience
Mesh:
Year: 2017 PMID: 28718765 PMCID: PMC5550281 DOI: 10.7554/eLife.26975
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140