Routing Hippocampal Information Flow through Parvalbumin Interneuron Plasticity in Area CA2.

The hippocampus is critical for the formation of episodic memory. It is, therefore, important to understand intra-hippocampal circuitry, especially in the often overlooked area CA2. Using specific transgenic mouse lines combined with opto- and chemogenetics, we show that local plasticity of parvalbumin-expressing interneurons in area CA2 allows CA3 input to recruit CA2 pyramidal neurons (PNs), thereby increasing the excitatory drive between CA3 and CA1. CA2 PNs provide both stronger excitation and larger feed-forward inhibition onto deep, compared with superficial, CA1 PNs. This feed-forward inhibition, largely mediated by parvalbumin-expressing interneurons, normalizes the excitatory drive onto deep and superficial CA1 PNs. Finally, we identify a target of CA2 in area CA1, i.e., CA1 PNs, whose soma are located in stratum radiatum. These data provide insight into local hippocampal circuitry and reveal how localized plasticity can potentially control information flow in the larger hippocampal network.

[1]  Alex M. Thomson,et al.  Distribution of interneurons in the CA2 region of the rat hippocampus , 2014, Front. Neuroanat..

[2]  Vivien Chevaleyre,et al.  Inhibitory Plasticity Permits the Recruitment of CA2 Pyramidal Neurons by CA31,2,3 , 2015, eNeuro.

[3]  Y. Ben‐Ari,et al.  Blocking GABA(A) inhibition reveals AMPA- and NMDA-receptor-mediated polysynaptic responses in the CA1 region of the rat hippocampus. , 1997, Journal of neurophysiology.

[4]  Daniel Gomez-Dominguez,et al.  Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples , 2015, Nature Neuroscience.

[5]  S. Dudek,et al.  Role of the vasopressin 1b receptor in rodent aggressive behavior and synaptic plasticity in hippocampal area CA2 , 2014, Molecular Psychiatry.

[6]  Mattias P. Karlsson,et al.  A hippocampal network for spatial coding during immobility and sleep , 2016, Nature.

[7]  E. L. Stevenson,et al.  Lesions to the CA2 region of the hippocampus impair social memory in mice , 2014, The European journal of neuroscience.

[8]  N. Tamamaki,et al.  Three-dimensional analysis of the whole axonal arbors originating from single CA2 pyramidal neurons in the rat hippocampus with the aid of a computer graphic technique , 1988, Brain Research.

[9]  S. Dudek,et al.  Caffeine-induced synaptic potentiation in hippocampal CA2 neurons , 2011, Nature Neuroscience.

[10]  Dheeraj S. Roy,et al.  Ventral CA1 neurons store social memory , 2016, Science.

[11]  S. Siegelbaum,et al.  Strong CA2 Pyramidal Neuron Synapses Define a Powerful Disynaptic Cortico-Hippocampal Loop , 2010, Neuron.

[12]  David H. Brann,et al.  Input-Timing-Dependent Plasticity in the Hippocampal CA2 Region and Its Potential Role in Social Memory , 2017, Neuron.

[13]  Vivien Chevaleyre,et al.  Delta-Opioid Receptors Mediate Unique Plasticity onto Parvalbumin-Expressing Interneurons in Area CA2 of the Hippocampus , 2013, The Journal of Neuroscience.

[14]  Thomas J. McHugh,et al.  Chronic Loss of CA2 Transmission Leads to Hippocampal Hyperexcitability , 2017, Neuron.

[15]  Yun-Sik Choi,et al.  Synaptic Plasticity (and the Lack Thereof) in Hippocampal CA2 Neurons , 2007, The Journal of Neuroscience.

[16]  N. P. Poolos,et al.  Reversed somatodendritic Ih gradient in a class of rat hippocampal neurons with pyramidal morphology , 2007, The Journal of physiology.

[17]  G. Buzsáki,et al.  Hippocampal CA1 pyramidal cells form functionally distinct sublayers , 2011, Nature Neuroscience.

[18]  Y. Yaari,et al.  Unique Properties of NMDA Receptors Enhance Synaptic Excitation of Radiatum Giant Cells in Rat Hippocampus , 2000, The Journal of Neuroscience.

[19]  Joseph A. Gogos,et al.  Age-Dependent Specific Changes in Area CA2 of the Hippocampus and Social Memory Deficit in a Mouse Model of the 22q11.2 Deletion Syndrome , 2016, Neuron.

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

[21]  F. Helmchen,et al.  Spatially segregated feedforward and feedback neurons support differential odor processing in the lateral entorhinal cortex , 2016, Nature Neuroscience.

[22]  J. Vonesch,et al.  Distribution of delta opioid receptor-expressing neurons in the mouse hippocampus , 2012, Neuroscience.

[23]  N. Bannister,et al.  Dendritic morphology of CA1 pyramidal neurones from the rat hippocampus: I. Branching patterns , 1995, The Journal of comparative neurology.

[24]  J. O’Neill,et al.  Gamma Oscillatory Firing Reveals Distinct Populations of Pyramidal Cells in the CA1 Region of the Hippocampus , 2008, The Journal of Neuroscience.

[25]  K. Tóth,et al.  Stratum radiatum giant cells: a type of principal cell in the rat hippocampus , 1998, The European journal of neuroscience.

[26]  Fraser T. Sparks,et al.  Hippocampal CA2 Activity Patterns Change over Time to a Larger Extent than between Spatial Contexts , 2015, Neuron.

[27]  Ian R. Wickersham,et al.  Cell type-specific genetic and optogenetic tools reveal novel hippocampal CA2 circuits , 2013, Nature Neuroscience.

[28]  Antal Berényi,et al.  Role of Hippocampal CA2 Region in Triggering Sharp-Wave Ripples , 2016, Neuron.

[29]  Azahara Oliva,et al.  A hippocampal circuit linking dorsal CA2 to ventral CA1 critical for social memory dynamics , 2018, Nature Communications.

[30]  A. Losonczy,et al.  CA1 pyramidal cell diversity enabling parallel information processing in the hippocampus , 2018, Nature Neuroscience.

[31]  S. Siegelbaum,et al.  The hippocampal CA2 region is essential for social memory , 2014, Nature.

[32]  Thomas J McHugh,et al.  The Hippocampal CA2 Ensemble Is Sensitive to Contextual Change , 2014, The Journal of Neuroscience.

[33]  M. Webster,et al.  Molecular abnormalities of the hippocampus in severe psychiatric illness: postmortem findings from the Stanley Neuropathology Consortium , 2004, Molecular Psychiatry.

[34]  T. van Groen,et al.  Extrinsic projections from area CA1 of the rat hippocampus: Olfactory, cortical, subcortical, and bilateral hippocampal formation projections , 1990, The Journal of comparative neurology.

[35]  N. Lozovaya,et al.  Latent N-methyl-D-aspartate receptors in the recurrent excitatory pathway between hippocampal CA1 pyramidal neurons: Ca(2+)-dependent activation by blocking A1 adenosine receptors. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[36]  Lindsey L. Glickfeld,et al.  Complementary Modulation of Somatic Inhibition by Opioids and Cannabinoids , 2008, The Journal of Neuroscience.

[37]  Attila Losonczy,et al.  Parvalbumin-Positive Basket Cells Differentiate among Hippocampal Pyramidal Cells , 2014, Neuron.