@article{1ea6c868594442dea6b66abf58086406,
title = "Learning and attention increase visual response selectivity through distinct mechanisms",
abstract = "Selectivity of cortical neurons for sensory stimuli can increase across days as animals learn their behavioral relevance and across seconds when animals switch attention. While both phenomena occur in the same circuit, it is unknown whether they rely on similar mechanisms. We imaged primary visual cortex as mice learned a visual discrimination task and subsequently performed an attention switching task. Selectivity changes due to learning and attention were uncorrelated in individual neurons. Selectivity increases after learning mainly arose from selective suppression of responses to one of the stimuli but from selective enhancement and suppression during attention. Learning and attention differentially affected interactions between excitatory and PV, SOM, and VIP inhibitory cells. Circuit modeling revealed that cell class-specific top-down inputs best explained attentional modulation, while reorganization of local functional connectivity accounted for learning-related changes. Thus, distinct mechanisms underlie increased discriminability of relevant sensory stimuli across longer and shorter timescales.",
keywords = "Animals, Attention/physiology, Discrimination, Psychological, Learning/physiology, Mice, Neurons/physiology, Visual Perception/physiology",
author = "Jasper Poort and Katharina Wilmes and Antonin Blot and Angus Chadwick and Maneesh Sahani and Claudia Clopath and Thomas Mrsic-Flogel and Sonja Hofer and Adil Khan",
note = "Funding Information: We thank the GENIE Program and Janelia Research Campus of the Howard Hughes Medical Institute for making GCaMP6 material available. This work was supported by the European Research Council (S.B.H., HigherVision 337797 ; T.D.M.-F., NeuroV1sion 616509 ), the SNSF (S.B.H., 31003A_169525 ; A.G.K., PZ00P3_168046 ), EMBO (A.B., ALTF 74-2014 ), the Wellcome Trust (A.G.K., 206222/Z/17/Z ; J.P., 211258/Z/18/Z ; C.C., 200790/Z/16/Z ; T.D.M.-F. and S.B.H., 090843/F/09/Z ), the BBSRC (C.C., BB/N013956/1 and BB/N019008/1 ; A.G.K., BB/S015809/1 ), the EPSRC (C.C., EP/R035806/1 ), the Simons Foundation (C.C., 564408 ; M.S., SCGB 323228 and 543039 ), the Gatsby Charitable Foundation (M.S., T.D.M.-F., and S.B.H., GAT3361 ), the DFG ( KAW 398005926 ), and Biozentrum core funds (University of Basel ). Funding Information: We thank the GENIE Program and Janelia Research Campus of the Howard Hughes Medical Institute for making GCaMP6 material available. This work was supported by the European Research Council (S.B.H. HigherVision 337797; T.D.M.-F. NeuroV1sion 616509), the SNSF (S.B.H. 31003A_169525; A.G.K. PZ00P3_168046), EMBO (A.B. ALTF 74-2014), the Wellcome Trust (A.G.K. 206222/Z/17/Z; J.P. 211258/Z/18/Z; C.C. 200790/Z/16/Z; T.D.M.-F. and S.B.H. 090843/F/09/Z), the BBSRC (C.C. BB/N013956/1 and BB/N019008/1; A.G.K. BB/S015809/1), the EPSRC (C.C. EP/R035806/1), the Simons Foundation (C.C. 564408; M.S. SCGB 323228 and 543039), the Gatsby Charitable Foundation (M.S. T.D.M.-F. and S.B.H. GAT3361), the DFG (KAW 398005926), and Biozentrum core funds (University of Basel). J.P. T.D.M.-F. S.B.H. and A.G.K. designed the experiments. J.P. and A.G.K. performed the experiments and analyzed the data. K.W. developed and analyzed the circuit model, with supervision from C.C. A.C. developed and analyzed the MVAR model, with supervision from M.S. A.B. performed the immunostaining and contributed to the post hoc cell-matching procedure. All of the authors discussed the data. J.P. and A.G.K. wrote the article, with input from all of the authors. The authors declare no competing interests Publisher Copyright: {\textcopyright} 2021 The Authors",
year = "2022",
month = feb,
day = "16",
doi = "10.1016/j.neuron.2021.11.016",
language = "English",
volume = "110",
pages = "686--697.e6",
journal = "Neuron",
issn = "0896-6273",
publisher = "Cell Press",
number = "4",
}