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Rewarding Capacity of Optogenetically Activating a Giant GABAergic Central-Brain Interneuron in Larval Drosophila.
Mancini, Nino; Thoener, Juliane; Tafani, Esmeralda; Pauls, Dennis; Mayseless, Oded; Strauch, Martin; Eichler, Katharina; Champion, Andrew; Kobler, Oliver; Weber, Denise; Sen, Edanur; Weiglein, Alice; Hartenstein, Volker; Chytoudis-Peroudis, Charalampos-Chrysovalantis; Jovanic, Tihana; Thum, Andreas S; Rohwedder, Astrid; Schleyer, Michael; Gerber, Bertram.
Afiliação
  • Mancini N; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany nino.mancini@mpfi.org bertram.gerber@lin-magdeburg.de.
  • Thoener J; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany.
  • Tafani E; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany.
  • Pauls D; Department of Animal Physiology, Institute of Biology, Leipzig University, Leipzig, 04103, Germany.
  • Mayseless O; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
  • Strauch M; Institute of Imaging and Computer Vision, RWTH Aachen University, Aachen, 52074, Germany.
  • Eichler K; Institute of Neurobiology, University of Puerto Rico Medical Science Campus, Old San Juan, Puerto Rico, 00901.
  • Champion A; Department of Physiology, Development and Neuroscience, Cambridge University, Cambridge, CB2 3EL, United Kingdom.
  • Kobler O; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, 20147, Virginia.
  • Weber D; Leibniz Institute for Neurobiology, Combinatorial Neuroimaging Core Facility, Magdeburg, 39118, Germany.
  • Sen E; Department of Genetics, Institute of Biology, Leipzig University, Leipzig, 04103, Germany.
  • Weiglein A; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany.
  • Hartenstein V; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany.
  • Chytoudis-Peroudis CC; University of California, Department of Molecular, Cell and Developmental Biology, Los Angeles, California 90095-1606.
  • Jovanic T; Université Paris-Saclay, Centre National de la Recherche Scientifique, Institut des neurosciences Paris-Saclay, Saclay, 91400, France.
  • Thum AS; Université Paris-Saclay, Centre National de la Recherche Scientifique, Institut des neurosciences Paris-Saclay, Saclay, 91400, France.
  • Rohwedder A; Department of Genetics, Institute of Biology, Leipzig University, Leipzig, 04103, Germany.
  • Schleyer M; Department of Genetics, Institute of Biology, Leipzig University, Leipzig, 04103, Germany.
  • Gerber B; Leibniz Institute for Neurobiology, Department Genetics of Learning and Memory, Magdeburg, 39118, Germany.
J Neurosci ; 43(44): 7393-7428, 2023 11 01.
Article em En | MEDLINE | ID: mdl-37734947
ABSTRACT
Larvae of the fruit fly Drosophila melanogaster are a powerful study case for understanding the neural circuits underlying behavior. Indeed, the numerical simplicity of the larval brain has permitted the reconstruction of its synaptic connectome, and genetic tools for manipulating single, identified neurons allow neural circuit function to be investigated with relative ease and precision. We focus on one of the most complex neurons in the brain of the larva (of either sex), the GABAergic anterior paired lateral neuron (APL). Using behavioral and connectomic analyses, optogenetics, Ca2+ imaging, and pharmacology, we study how APL affects associative olfactory memory. We first provide a detailed account of the structure, regional polarity, connectivity, and metamorphic development of APL, and further confirm that optogenetic activation of APL has an inhibiting effect on its main targets, the mushroom body Kenyon cells. All these findings are consistent with the previously identified function of APL in the sparsening of sensory representations. To our surprise, however, we found that optogenetically activating APL can also have a strong rewarding effect. Specifically, APL activation together with odor presentation establishes an odor-specific, appetitive, associative short-term memory, whereas naive olfactory behavior remains unaffected. An acute, systemic inhibition of dopamine synthesis as well as an ablation of the dopaminergic pPAM neurons impair reward learning through APL activation. Our findings provide a study case of complex circuit function in a numerically simple brain, and suggest a previously unrecognized capacity of central-brain GABAergic neurons to engage in dopaminergic reinforcement.SIGNIFICANCE STATEMENT The single, identified giant anterior paired lateral (APL) neuron is one of the most complex neurons in the insect brain. It is GABAergic and contributes to the sparsening of neuronal activity in the mushroom body, the memory center of insects. We provide the most detailed account yet of the structure of APL in larval Drosophila as a neurogenetically accessible study case. We further reveal that, contrary to expectations, the experimental activation of APL can exert a rewarding effect, likely via dopaminergic reward pathways. The present study both provides an example of unexpected circuit complexity in a numerically simple brain, and reports an unexpected effect of activity in central-brain GABAergic circuits.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Drosophila / Drosophila melanogaster Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Drosophila / Drosophila melanogaster Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2023 Tipo de documento: Article