Publication | Open Access
Mushroom body output neurons encode valence and guide memory-based action selection in Drosophila
751
Citations
139
References
2014
Year
Brain MechanismCircuit NeuroscienceAffective NeuroscienceMushroom BodySensory SystemsSynaptic SignalingSocial SciencesNeural MechanismSensory NeuroscienceCognitive ScienceMemory-based Action SelectionBehavioral NeuroscienceMbon PerturbationNervous SystemMbon NetworkBiologyNeurobiological MechanismComputational NeuroscienceCellular NeuroscienceNeural CircuitsNeuroscienceMedicineAnimal Behavior
We have content for each. Background: combine all three background sentences into one sentence. Summarize: "Animals discriminate stimuli, learn predictive value, and use this knowledge to modify behavior; in Drosophila, the mushroom body (MB) is key, with sensory stimuli sparsely represented by ~2000 Kenyon cells converging onto 34 output neurons (MBONs) of 21 types." Need to keep concise. Maybe: "Animals discriminate stimuli, learn their predictive value, and modify behavior; in Drosophila, the mushroom body, where ~2000 Kenyon cells sparsely encode sensory inputs onto 34 output neurons of 21 types, plays a key role in these processes." That is one sentence.
Animals discriminate stimuli, learn their predictive value and use this knowledge to modify their behavior. In Drosophila, the mushroom body (MB) plays a key role in these processes. Sensory stimuli are sparsely represented by ∼2000 Kenyon cells, which converge onto 34 output neurons (MBONs) of 21 types. We studied the role of MBONs in several associative learning tasks and in sleep regulation, revealing the extent to which information flow is segregated into distinct channels and suggesting possible roles for the multi-layered MBON network. We also show that optogenetic activation of MBONs can, depending on cell type, induce repulsion or attraction in flies. The behavioral effects of MBON perturbation are combinatorial, suggesting that the MBON ensemble collectively represents valence. We propose that local, stimulus-specific dopaminergic modulation selectively alters the balance within the MBON network for those stimuli. Our results suggest that valence encoded by the MBON ensemble biases memory-based action selection.
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