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Neuron-type-specific signals for reward and punishment in the ventral tegmental area
Naturevolume 482, pages85–88 (2012)Cite this article
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Abstract
Dopamine has a central role in motivation and reward. Dopaminergic neurons in the ventral tegmental area (VTA) signal the discrepancy between expected and actual rewards (that is, reward prediction error)1,2,3, but how they compute such signals is unknown. We recorded the activity of VTA neurons while mice associated different odour cues with appetitive and aversive outcomes. We found three types of neuron based on responses to odours and outcomes: approximately half of the neurons (type I, 52%) showed phasic excitation after reward-predicting odours and rewards in a manner consistent with reward prediction error coding; the other half of neurons showed persistent activity during the delay between odour and outcome that was modulated positively (type II, 31%) or negatively (type III, 18%) by the value of outcomes. Whereas the activity of type I neurons was sensitive to actual outcomes (that is, when the reward was delivered as expected compared to when it was unexpectedly omitted), the activity of type II and type III neurons was determined predominantly by reward-predicting odours. We ‘tagged’ dopaminergic and GABAergic neurons with the light-sensitive protein channelrhodopsin-2 and identified them based on their responses to optical stimulation while recording. All identified dopaminergic neurons were of type I and all GABAergic neurons were of type II. These results show that VTA GABAergic neurons signal expected reward, a key variable for dopaminergic neurons to calculate reward prediction error.
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Acknowledgements
We thank M. Meister, V. N. Murthy, J. D. Schall and R. P. Heitz for comments, C. Dulac for sharing resources, C. I. Moore, J. Ritt and J. Siegle for advice about microdrives, K. Deisseroth for the AAV-FLEX-ChR2 construct, and E. Soucy and J. Greenwood for technical support. This work was supported by a Howard Hughes Medical Institute Fellowship from the Helen Hay Whitney Foundation (J.Y.C.); the Human Frontiers Science Program (S.H.); a Howard Hughes Medical Institute Collaborative Innovation Award, a Smith Family New Investigator Award, the Alfred Sloan Foundation, the Milton Fund (N.U.); F32 DK078478, P30 DK046200 (L.V.); and R01 DK075632, R01 DK089044, P30 DK046200, P30 DK057521 (B.B.L.).
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Jeremiah Y. Cohen and Sebastian Haesler: These authors contributed equally to this work.
Authors and Affiliations
Department of Molecular and Cellular Biology, Center for Brain Science, Harvard University, Cambridge, 02138, Massachusetts, USA
Jeremiah Y. Cohen, Sebastian Haesler & Naoshige Uchida
Division of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, 02215, Massachusetts, USA
Linh Vong & Bradford B. Lowell
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Contributions
J.Y.C. and S.H. collected and analysed data. J.Y.C., S.H. and N.U. designed experiments and wrote the paper. L.V. and B.B.L. generatedVgat-Cre mice.
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Correspondence toNaoshige Uchida.
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Cohen, J., Haesler, S., Vong, L.et al. Neuron-type-specific signals for reward and punishment in the ventral tegmental area.Nature482, 85–88 (2012). https://doi.org/10.1038/nature10754
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