Value-guided remapping of sensory cortex by lateral orbitofrontal cortex.
Adaptation, Psychological
Animals
Brain Mapping
Calcium Signaling
Decision Making
/ physiology
Discrimination, Psychological
/ physiology
Male
Mice
Neuronal Plasticity
/ physiology
Physical Stimulation
Prefrontal Cortex
/ cytology
Reversal Learning
/ physiology
Sensory Receptor Cells
/ metabolism
Somatosensory Cortex
/ cytology
Touch Perception
/ physiology
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
16
10
2019
accepted:
22
06
2020
pubmed:
5
9
2020
medline:
22
9
2020
entrez:
5
9
2020
Statut:
ppublish
Résumé
Adaptive behaviour crucially depends on flexible decision-making, which in mammals relies on the frontal cortex, specifically the orbitofrontal cortex (OFC)
Identifiants
pubmed: 32884146
doi: 10.1038/s41586-020-2704-z
pii: 10.1038/s41586-020-2704-z
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
245-250Subventions
Organisme : European Research Council
Pays : International
Références
Fettes, P., Schulze, L. & Downar, J. Cortico-striatal-thalamic loop circuits of the orbitofrontal cortex: promising therapeutic targets in psychiatric illness. Front. Syst. Neurosci. 11, 25 (2017).
pubmed: 28496402
pmcid: 5406748
Miller, E. K. The prefrontal cortex and cognitive control. Nat. Rev. Neurosci. 1, 59–65 (2000).
pubmed: 11252769
Fuster, J. M. The prefrontal cortex—an update: time is of the essence. Neuron 30, 319–333 (2001).
pubmed: 11394996
Rolls, E. T. The orbitofrontal cortex and reward. Cereb. Cortex 10, 284–294 (2000).
pubmed: 10731223
Izquierdo, A. Functional heterogeneity within rat orbitofrontal cortex in reward learning and decision making. J. Neurosci. 37, 10529–10540 (2017).
pubmed: 29093055
pmcid: 6596524
Rudebeck, P. H. & Murray, E. A. The orbitofrontal oracle: cortical mechanisms for the prediction and evaluation of specific behavioral outcomes. Neuron 84, 1143–1156 (2014).
pubmed: 25521376
pmcid: 4271193
Rushworth, M. F. S., Noonan, M. P., Boorman, E. D., Walton, M. E. & Behrens, T. E. Frontal cortex and reward-guided learning and decision-making. Neuron 70, 1054–1069 (2011).
pubmed: 21689594
Wallis, J. D. Orbitofrontal cortex and its contribution to decision-making. Annu. Rev. Neurosci. 30, 31–56 (2007).
pubmed: 17417936
Carlén, M. What constitutes the prefrontal cortex? Science 358, 478–482 (2017).
pubmed: 29074767
Chen, J. L., Carta, S., Soldado-Magraner, J., Schneider, B. L. & Helmchen, F. Behaviour-dependent recruitment of long-range projection neurons in somatosensory cortex. Nature 499, 336–340 (2013).
pubmed: 23792559
Chen, J. L. et al. Pathway-specific reorganization of projection neurons in somatosensory cortex during learning. Nat. Neurosci. 18, 1101–1108 (2015).
pubmed: 26098757
Petersen, C. C. H. Sensorimotor processing in the rodent barrel cortex. Nat. Rev. Neurosci. 20, 533–546 (2019).
pubmed: 31367018
Bissonette, G. B., Schoenbaum, G., Roesch, M. R. & Powell, E. M. Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex. Biol. Psychiatry 77, 454–464 (2015).
pubmed: 25193243
Jennings, J. H. et al. Interacting neural ensembles in orbitofrontal cortex for social and feeding behaviour. Nature 565, 645–649 (2019).
pubmed: 30651638
pmcid: 6447429
Pho, G. N., Goard, M. J., Woodson, J., Crawford, B. & Sur, M. Task-dependent representations of stimulus and choice in mouse parietal cortex. Nat. Commun. 9, 2596 (2018).
pubmed: 29968709
pmcid: 6030204
Ramesh, R. N., Burgess, C. R., Sugden, A. U., Gyetvan, M. & Andermann, M. L. Intermingled ensembles in visual association cortex encode stimulus identity or predicted outcome. Neuron 100, 900–915.e9 (2018).
pubmed: 30318413
pmcid: 6250571
Voigt, F. F. et al. The mesoSPIM initiative: open-source light-sheet microscopes for imaging cleared tissue. Nat. Methods 16, 1105–1108 (2019).
pubmed: 31527839
pmcid: 6824906
Bastos, A. M. et al. Canonical microcircuits for predictive coding. Neuron 76, 695–711 (2012).
pubmed: 23177956
pmcid: 3777738
Schoenbaum, G., Roesch, M. R., Stalnaker, T. A. & Takahashi, Y. K. A new perspective on the role of the orbitofrontal cortex in adaptive behaviour. Nat. Rev. Neurosci. 10, 885–892 (2009).
pubmed: 19904278
pmcid: 2835299
Schultz, W. & Dickinson, A. Neuronal coding of prediction errors. Annu. Rev. Neurosci. 23, 473–500 (2000).
pubmed: 10845072
Sul, J. H., Kim, H., Huh, N., Lee, D. & Jung, M. W. Distinct roles of rodent orbitofrontal and medial prefrontal cortex in decision making. Neuron 66, 449–460 (2010).
pubmed: 20471357
pmcid: 2872629
Chudasama, Y. & Robbins, T. W. Dissociable contributions of the orbitofrontal and infralimbic cortex to Pavlovian autoshaping and discrimination reversal learning: further evidence for the functional heterogeneity of the rodent frontal cortex. J. Neurosci. 23, 8771–8780 (2003).
pubmed: 14507977
pmcid: 6740430
Groman, S. M. et al. Orbitofrontal circuits control multiple reinforcement-learning processes. Neuron 103, 734–746.e3 (2019).
Hattori, R., Danskin, B., Babic, Z., Mlynaryk, N. & Komiyama, T. Area-specificity and plasticity of history-dependent value coding during learning. Cell 177, 1858–1872 (2019).
pubmed: 31080067
pmcid: 6663310
Saez, R. A., Saez, A., Paton, J. J., Lau, B. & Salzman, C. D. Distinct roles for the amygdala and orbitofrontal cortex in representing the relative amount of expected reward. Neuron 95, 70–77.e3 (2017).
pubmed: 28683271
pmcid: 5710843
Rikhye, R. V., Gilra, A. & Halassa, M. M. Thalamic regulation of switching between cortical representations enables cognitive flexibility. Nat. Neurosci. 21, 1753–1763 (2018).
pubmed: 30455456
pmcid: 7225728
Shuler, M. G. & Bear, M. F. Reward timing in the primary visual cortex. Science 311, 1606–1609 (2006).
pubmed: 16543459
Chéreau, R. et al. Dynamic perceptual feature selectivity in primary somatosensory cortex upon reversal learning. Nat. Commun. 11, 3245 (2020).
Bari, A. et al. Serotonin modulates sensitivity to reward and negative feedback in a probabilistic reversal learning task in rats. Neuropsychopharmacology 35, 1290–1301 (2010).
pubmed: 20107431
pmcid: 3055347
Isaacson, J. S. & Scanziani, M. How inhibition shapes cortical activity. Neuron 72, 231–243 (2011).
pubmed: 22017986
pmcid: 3236361
Neftci, E. O. & Averbeck, B. B. Reinforcement learning in artificial and biological systems. Nat. Mach. Intell. 1, 133–143 (2019).
Mayford, M. et al. Control of memory formation through regulated expression of a CaMKII transgene. Science 274, 1678–1683 (1996).
pubmed: 8939850
Madisen, L. et al. Transgenic mice for intersectional targeting of neural sensors and effectors with high specificity and performance. Neuron 85, 942–958 (2015).
pubmed: 25741722
pmcid: 4365051
Harris, J. A. et al. Anatomical characterization of Cre driver mice for neural circuit mapping and manipulation. Front. Neural Circuits 8, 76 (2014).
pubmed: 25071457
pmcid: 4091307
Carandini, M. & Churchland, A. K. Probing perceptual decisions in rodents. Nat. Neurosci. 16, 824–831 (2013).
pubmed: 23799475
pmcid: 4105200
Bailey, K. R. & Crawley, J. N. in Methods in Behavioral Analysis in Neuroscience (eds Bailey, K. R., Crawley, J. N. & Buccafusco, J. J.) Ch. 5 (CRC, 2009).
Farr, T. D., Liu, L., Colwell, K. L., Whishaw, I. Q. & Metz, G. A. Bilateral alteration in stepping pattern after unilateral motor cortex injury: a new test strategy for analysis of skilled limb movements in neurological mouse models. J. Neurosci. Methods 153, 104–113 (2006).
pubmed: 16309746
Banerjee, A. et al. Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome. Proc. Natl Acad. Sci. USA 113, E7287–E7296 (2016).
pubmed: 27803317
Yang, B. et al. Single-cell phenotyping within transparent intact tissue through whole-body clearing. Cell 158, 945–958 (2014).
pubmed: 25088144
pmcid: 4153367
Chung, K. et al. Structural and molecular interrogation of intact biological systems. Nature 497, 332–337 (2013).
pubmed: 23575631
pmcid: 4092167
Gomez, J. L. et al. Chemogenetics revealed: DREADD occupancy and activation via converted clozapine. Science 357, 503–507 (2017).
pubmed: 28774929
pmcid: 7309169
Gilad, A., Gallero-Salas, Y., Groos, D. & Helmchen, F. Behavioral strategy determines frontal or posterior location of short-term memory in neocortex. Neuron 99, 814–828.e7 (2018).
pubmed: 30100254
Langer, D. et al. HelioScan: a software framework for controlling in vivo microscopy setups with high hardware flexibility, functional diversity and extendibility. J. Neurosci. Methods 215, 38–52 (2013).
pubmed: 23416135
Guo, Z. V. et al. Flow of cortical activity underlying a tactile decision in mice. Neuron 81, 179–194 (2014).
pubmed: 24361077
Sreenivasan, V. et al. Movement initiation signals in mouse whisker motor cortex. Neuron 92, 1368–1382 (2016).
pubmed: 28009277
pmcid: 5196025
Huber, D. et al. Multiple dynamic representations in the motor cortex during sensorimotor learning. Nature 484, 473–478 (2012).
pubmed: 22538608
pmcid: 4601999