Impaired hippocampal place cell dynamics in a mouse model of the 22q11.2 deletion

Hippocampal place cells represent the cellular substrate of episodic memory. Place cell ensembles reorganize to support learning but must also maintain stable representations to facilitate memory recall. Despite extensive research, the learning-related role of place cell dynamics in health and disease remains elusive. Using chronic two-photon Ca2+ imaging in hippocampal area CA1 of wild-type and Df(16)A+/− mice, an animal model of 22q11.2 deletion syndrome, one of the most common genetic risk factors for cognitive dysfunction and schizophrenia, we found that goal-oriented learning in wild-type mice was supported by stable spatial maps and robust remapping of place fields toward the goal location. Df(16)A+/− mice showed a significant learning deficit accompanied by reduced spatial map stability and the absence of goal-directed place cell reorganization. These results expand our understanding of the hippocampal ensemble dynamics supporting cognitive flexibility and demonstrate their importance in a model of 22q11.2-associated cognitive dysfunction.

[1]  D. Tank,et al.  Imaging Large-Scale Neural Activity with Cellular Resolution in Awake, Mobile Mice , 2007, Neuron.

[2]  William W Lytton,et al.  Unmasking the CA1 Ensemble Place Code by Exposures to Small and Large Environments: More Place Cells and Multiple, Irregularly Arranged, and Expanded Place Fields in the Larger Space , 2008, The Journal of Neuroscience.

[3]  Karl Peter Giese,et al.  Experience-Dependent Increase in CA1 Place Cell Spatial Information, But Not Spatial Reproducibility, Is Dependent on the Autophosphorylation of the α-Isoform of the Calcium/Calmodulin-Dependent Protein Kinase II , 2007, The Journal of Neuroscience.

[4]  Paul Pavlidis,et al.  Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model , 2008, Nature Genetics.

[5]  Charan Ranganath,et al.  The Cognitive Neuroscience of Memory Function and Dysfunction in Schizophrenia , 2008, Biological Psychiatry.

[6]  Ariane S Etienne,et al.  Path integration in mammals , 2004, Hippocampus.

[7]  Paul J. Harrison,et al.  Neuropathological studies of synaptic connectivity in the hippocampal formation in schizophrenia , 2001, Hippocampus.

[8]  Conor Liston,et al.  Projections from neocortex mediate top-down control of memory retrieval , 2015, Nature.

[9]  R. Passingham The hippocampus as a cognitive map J. O'Keefe & L. Nadel, Oxford University Press, Oxford (1978). 570 pp., £25.00 , 1979, Neuroscience.

[10]  Joseph A. Gogos,et al.  Molecular Substrates of Altered Axonal Growth and Brain Connectivity in a Mouse Model of Schizophrenia , 2015, Neuron.

[11]  R. Hampson,et al.  Hippocampal place cells: stereotypy and plasticity , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  L. Nadel,et al.  The Hippocampus as a Cognitive Map , 1978 .

[13]  Tony J. Simon,et al.  22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia , 2010, Nature Reviews Neuroscience.

[14]  Bruno Poucet,et al.  Goal-Related Activity in Hippocampal Place Cells , 2007, The Journal of Neuroscience.

[15]  Michael Lagler,et al.  Behavior-dependent specialization of identified hippocampal interneurons , 2012, Nature Neuroscience.

[16]  P. Somogyi,et al.  Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo , 2003, Nature.

[17]  William R Holmes,et al.  Analysis and comparison of morphological reconstructions of hippocampal field CA1 pyramidal cells , 2005, Hippocampus.

[18]  J. Mukai,et al.  Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion , 2009, Neuroscience Research.

[19]  Omar J. Ahmed,et al.  The hippocampal rate code: anatomy, physiology and theory , 2009, Trends in Neurosciences.

[20]  T. Ono,et al.  Task-dependent representations in rat hippocampal place neurons. , 1997, Journal of neurophysiology.

[21]  Joseph D. Monaco,et al.  Attentive Scanning Behavior Drives One-Trial Potentiation of Hippocampal Place Fields , 2014, Nature Neuroscience.

[22]  Attila Losonczy,et al.  Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1 , 2016, Neuron.

[23]  Matthew A. Wilson,et al.  Impaired Hippocampal Ripple-Associated Replay in a Mouse Model of Schizophrenia , 2013, Neuron.

[24]  B. McNaughton,et al.  Experience-dependent, asymmetric expansion of hippocampal place fields. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Bruce L. McNaughton,et al.  An Information-Theoretic Approach to Deciphering the Hippocampal Code , 1992, NIPS.

[26]  G. Buzsáki,et al.  Interneurons of the hippocampus , 1998, Hippocampus.

[27]  Jeffrey D. Zaremba,et al.  Distinct Contribution of Adult-Born Hippocampal Granule Cells to Context Encoding , 2016, Neuron.

[28]  Attila Losonczy,et al.  Dendritic Inhibition in the Hippocampus Supports Fear Learning , 2014, Science.

[29]  Hongbo Jia,et al.  In vivo two-photon imaging of sensory-evoked dendritic calcium signals in cortical neurons , 2011, Nature Protocols.

[30]  J. O’Keefe,et al.  Space in the brain: how the hippocampal formation supports spatial cognition , 2014, Philosophical Transactions of the Royal Society B: Biological Sciences.

[31]  R. Kahn,et al.  Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. , 2015, JAMA psychiatry.

[32]  Thomas J. Wills,et al.  Long-term plasticity in hippocampal place-cell representation of environmental geometry , 2002, Nature.

[33]  P. Somogyi,et al.  Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations , 2008, Science.

[34]  G. Buzsáki Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic memory and planning , 2015, Hippocampus.

[35]  Rosanna Weksberg,et al.  The schizophrenia phenotype in 22q11 deletion syndrome. , 2003, The American journal of psychiatry.

[36]  J. O'Keefe,et al.  The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. , 1971, Brain research.

[37]  A. Wagner,et al.  The hippocampal formation in schizophrenia. , 2010, The American journal of psychiatry.

[38]  J. O’Neill,et al.  The reorganization and reactivation of hippocampal maps predict spatial memory performance , 2010, Nature Neuroscience.

[39]  B L McNaughton,et al.  Dynamics of the hippocampal ensemble code for space. , 1993, Science.

[40]  Ashutosh Kumar Singh,et al.  The Elements of Statistical Learning: Data Mining, Inference, and Prediction , 2010 .

[41]  T. Goldberg,et al.  Episodic Memory in Schizophrenia , 2009, Neuropsychology Review.

[42]  G. Wahba,et al.  Bootstrap confidence intervals for smoothing splines and their comparison to bayesian confidence intervals , 1995 .

[43]  Eric A. Zilli,et al.  Gradual Translocation of Spatial Correlates of Neuronal Firing in the Hippocampus toward Prospective Reward Locations , 2006, Neuron.

[44]  G. Buzsáki,et al.  Memory, navigation and theta rhythm in the hippocampal-entorhinal system , 2013, Nature Neuroscience.

[45]  Attila Losonczy,et al.  Septo-hippocampal GABAergic signaling across multiple modalities in awake mice , 2013, Nature Neuroscience.

[46]  T. Freund,et al.  Different input and output properties characterize parvalbumin‐positive basket and Axo‐axonic cells in the hippocampal CA3 subfield , 2013, Hippocampus.

[47]  Ivan Soltesz,et al.  Quantitative assessment of CA1 local circuits: Knowledge base for interneuron‐pyramidal cell connectivity , 2013, Hippocampus.

[48]  H. Eichenbaum A cortical–hippocampal system for declarative memory , 2000, Nature Reviews Neuroscience.

[49]  K M Gothard,et al.  Dynamics of Mismatch Correction in the Hippocampal Ensemble Code for Space: Interaction between Path Integration and Environmental Cues , 1996, The Journal of Neuroscience.

[50]  B. Bogerts,et al.  Hippocampal CA1 deformity is related to symptom severity and antipsychotic dosage in schizophrenia. , 2013, Brain : a journal of neurology.

[51]  R. Kahn,et al.  Schizophrenia is a cognitive illness: time for a change in focus. , 2013, JAMA psychiatry.

[52]  Fraser T. Sparks,et al.  Neuronal code for extended time in the hippocampus , 2012, Proceedings of the National Academy of Sciences.

[53]  Lacey J. Kitch,et al.  Long-term dynamics of CA1 hippocampal place codes , 2013, Nature Neuroscience.

[54]  Joseph A. Gogos,et al.  Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia , 2014, Front. Synaptic Neurosci..

[55]  M. Moser,et al.  Impaired Recognition of the Goal Location during Spatial Navigation in Rats with Hippocampal Lesions , 2001, The Journal of Neuroscience.

[56]  Tobias Bast,et al.  The hippocampal learning-behavior translation and the functional significance of hippocampal dysfunction in schizophrenia , 2011, Current Opinion in Neurobiology.

[57]  P. Golshani,et al.  Frequency-invariant temporal ordering of interneuronal discharges during hippocampal oscillations in awake mice , 2012, Proceedings of the National Academy of Sciences.

[58]  J. Gordon,et al.  Developmental Inhibition of Gsk3 Rescues Behavioral and Neurophysiological Deficits in a Mouse Model of Schizophrenia Predisposition , 2016, Neuron.

[59]  E. Kandel,et al.  Increased Attention to Spatial Context Increases Both Place Field Stability and Spatial Memory , 2004, Neuron.

[60]  Lucien T. Thompson,et al.  Long-term stability of the place-field activity of single units recorded from the dorsal hippocampus of freely behaving rats , 1990, Brain Research.

[61]  Stefan R. Pulver,et al.  Ultra-sensitive fluorescent proteins for imaging neuronal activity , 2013, Nature.

[62]  L. Squire Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. , 1992, Psychological review.

[63]  L. Nadel,et al.  Decay happens: the role of active forgetting in memory , 2013, Trends in Cognitive Sciences.

[64]  L. Campbell,et al.  Visual scanpath abnormalities in 22q11.2 deletion syndrome: Is this a face specific deficit? , 2011, Psychiatry Research.

[65]  M. Fyhn,et al.  Hippocampal Neurons Responding to First-Time Dislocation of a Target Object , 2002, Neuron.

[66]  M. Moser,et al.  Understanding memory through hippocampal remapping , 2008, Trends in Neurosciences.

[67]  Attila Losonczy,et al.  SIMA: Python software for analysis of dynamic fluorescence imaging data , 2014, Front. Neuroinform..

[68]  Inah Lee,et al.  The relationship between the field-shifting phenomenon and representational coherence of place cells in CA1 and CA3 in a cue-altered environment. , 2007, Learning & memory.

[69]  T. Freund,et al.  Total Number and Ratio of Excitatory and Inhibitory Synapses Converging onto Single Interneurons of Different Types in the CA1 Area of the Rat Hippocampus , 1999, The Journal of Neuroscience.

[70]  W E Skaggs,et al.  Interactions between location and task affect the spatial and directional firing of hippocampal neurons , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[71]  H. Eichenbaum Memory: Organization and Control. , 2017, Annual review of psychology.

[72]  Mattias P. Karlsson,et al.  Network Dynamics Underlying the Formation of Sparse, Informative Representations in the Hippocampus , 2008, The Journal of Neuroscience.

[73]  S. Eliez,et al.  Encoding and retrieval processes in velo-cardio-facial syndrome (VCFS). , 2008, Neuropsychology.

[74]  Akira Sawa,et al.  Disordered Ripples Are a Common Feature of Genetically Distinct Mouse Models Relevant to Schizophrenia , 2015, Molecular Neuropsychiatry.

[75]  Lin Tian,et al.  Functional imaging of hippocampal place cells at cellular resolution during virtual navigation , 2010, Nature Neuroscience.

[76]  M. Andersson,et al.  Independent Codes for Spatial and Episodic Memory in Hippocampal Neuronal Ensembles , 2005 .