December 4, 2021

Linking hippocampal multiplexed tuning, Hebbian plasticity and navigation – Nature

  • 1.

    Morris, R. G. M. Synaptic plasticity and learning: selective impairment of learning in rats and blockade of long-term potentiation in vivo by the N-methyl-d-aspartate receptor antagonist AP5. J. Neurosci. 9, 3040–3057 (1989).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 2.

    Bliss, T. V. P. & Lømo, T. Long-lasting potentiation of synaptic transmission in the dentate area of the anesthetized rabbit following stimulation of the perforant path. J. Physiol. 232, 331–356 (1973).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 3.

    O’Keefe, J. & Dostrovsky, J. The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. Brain Res. 34, 171–175 (1971).

    PubMed 
    Article 

    Google Scholar
     

  • 4.

    Scoville, W. B. & Milner, B. Loss of recent memory after bilateral hippocampal lesions. J. Neurol. Neurosurg. Psychiatry 20, 11–21 (1957).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 5.

    Cushman, J. D. et al. Multisensory control of multimodal behavior: do the legs know what the tongue is doing? PLoS ONE 8, e80465 (2013).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 6.

    Blum, K. I. & Abbott, L. F. A model of spatial map formation in the hippocampus of the rat. Neural Comp. 8, 85–93 (1996).

    CAS 
    Article 

    Google Scholar
     

  • 7.

    Mehta, M. R., Quirk, M. C. & Wilson, M. A. Experience-dependent asymmetric shape of hippocampal receptive fields. Neuron 25, 707–715 (2000).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 8.

    Tsodyks, M. & Sejnowski, T. Associative memory and hippocampal place cells. Int. J. Neural Syst. 6, 81–86 (1995).


    Google Scholar
     

  • 9.

    McNaughton, B. L. et al. Deciphering the hippocampal polyglot: the hippocampus as a path integration system. J. Exp. Biol. 199, 173–185 (1996).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 10.

    Buzsáki, G. & Moser, E. I. Memory, navigation and theta rhythm in the hippocampal–entorhinal system. Nat. Neurosci. 16, 130–138 (2013).

    PubMed 
    PubMed Central 
    Article 
    CAS 

    Google Scholar
     

  • 11.

    Hollup, S. A., Molden, S., Donnett, J. G., Moser, M. B. & Moser, E. I. Accumulation of hippocampal place fields at the goal location in an annular watermaze task. J. Neurosci. 21, 1635–1644 (2001).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 12.

    Pfeiffer, B. E. & Foster, D. J. Hippocampal place-cell sequences depict future paths to remembered goals. Nature 497, 74–79 (2013).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 13.

    Xu, H., Baracskay, P., O’Neill, J. & Csicsvari, J. Assembly responses of hippocampal CA1 place cells predict learned behavior in goal-directed spatial tasks on the radial eight-arm maze. Neuron 101, 119–132 (2019).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 14.

    Mehta, M. R., Barnes, C. A. & McNaughton, B. L. Experience-dependent, asymmetric expansion of hippocampal place fields. Proc. Natl Acad. Sci. USA 94, 8918–8921 (1997).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 15.

    Mehta, M. R. & McNaughton, B. L. Expansion and shift of hippocampal place fields: evidence for synaptic potentiation during behavior. Comput. Neurosci. Trends Res. 741–745 (1997).

  • 16.

    Mehta, M. R. From synaptic plasticity to spatial maps and sequence learning. Hippocampus 25, 756–762 (2015).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 17.

    Tulving, E. Episodic memory: from mind to brain. Annu. Rev. Psychol. 53, 1–25 (2002).

    ADS 
    PubMed 
    Article 

    Google Scholar
     

  • 18.

    Baraduc, P. & Wirth, S. Schema cells in the macaque hippocampus. Science 363, 635–639 (2019).

    ADS 
    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 19.

    Pastalkova, E., Itskov, V., Amarasingham, A. & Buzsáki, G. Internally generated cell assembly sequences in the rat hippocampus. Science 321, 1322–1327 (2008).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 20.

    Ravassard, P. et al. Multisensory control of hippocampal spatiotemporal selectivity. Science 340, 1342–1346 (2013).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 21.

    Aghajan, Z. M. et al. Impaired spatial selectivity and intact phase precession in two-dimensional virtual reality. Nat. Neurosci. 18, 121–128 (2015).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 22.

    Villette, V., Malvache, A., Tressard, T., Dupuy, N. & Cossart, R. Internally recurring hippocampal sequences as a population template of spatiotemporal information. Neuron 88, 357–366 (2015).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 23.

    Sarel, A., Finkelstein, A., Las, L. & Ulanovsky, N. Vectorial representation of spatial goals in the hippocampus of bats. Science 355, 176–180 (2017).

    ADS 
    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 24.

    Markram, H., Lübke, J. & Frotscher, M. Regulation of synaptic efficacy by coincidence of postsynaptic APs and EPSPs. Science 275, 213–215 (1997).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 25.

    Bi, G. & Poo, M. Synaptic modifications in cultured hippocampal neurons: dependence on spike timing, synaptic strength, and postsynaptic cell type. J. Neurosci. 18, 10464–10472 (1998).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 26.

    Mehta, M. R. & Wilson, M. A. From hippocampus to V1: effect of LTP on spatio-temporal dynamics of receptive fields. Neurocomputing 32–33, 905–911 (2000).

    Article 

    Google Scholar
     

  • 27.

    Kentros, C. et al. Abolition of long-term stability of new hippocampal place cell maps by NMDA receptor blockade. Science 280, 2121–2126 (1998).

    ADS 
    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 28.

    Ekstrom, A. D., Meltzer, J., McNaughton, B. L. & Barnes, C. A. NMDA receptor antagonism blocks experience-dependent expansion of hippocampal ‘place fields’. Neuron 31, 631–638 (2001).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 29.

    Sato, M. et al. Hippocampus-dependent goal localization by head-fixed mice in virtual reality. eNeuro 4, ENEURO.0369-16.2017 (2017).

    Article 

    Google Scholar
     

  • 30.

    Rowland, L. H. et al. Selective cognitive impairments associated with NMDA receptor blockade in humans. Neuropsychopharmacology 30, 633–639 (2005).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 31.

    Dupret, D., O’Neill, J., Pleydell-Bouverie, B. & Csicsvari, J. The reorganization and reactivation of hippocampal maps predict spatial memory performance. Nat. Neurosci. 13, 995–1002 (2010).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 32.

    Gothard, K. M., Skaggs, W. E. & McNaughton, B. L. Dynamics of mismatch correction in the hippocampal ensemble code for space: interaction between path integration and environmental cues. J. Neurosci. 16, 8027–8040 (1996).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 33.

    Acharya, L., Aghajan, Z. M., Vuong, C., Moore, J. J. & Mehta, M. R. Causal influence of visual cues on hippocampal directional selectivity. Cell 164, 197–207 (2016).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 34.

    Ziv, Y. et al. Long-term dynamics of CA1 hippocampal place codes. Nat. Neurosci. 16, 264–266 (2013).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 35.

    Howard, L. R. et al. The hippocampus and entorhinal cortex encode the path and euclidean distances to goals during navigation. Curr. Biol. 24, 1331–1340 (2014).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 36.

    MacDonald, C. J., Lepage, K. Q., Eden, U. T. & Eichenbaum, H. Hippocampal ‘time cells’ bridge the gap in memory for discontiguous events. Neuron 71, 737–749 (2011).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 37.

    Gauthier, J. L. & Tank, D. W. A dedicated population for reward coding in the hippocampus. Neuron 99, 179–193 (2018).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 38.

    Leutgeb, S. et al. Independent codes for spatial and episodic memory in hippocampal neuronal ensembles. Science 309, 619–623 (2005).

    ADS 
    CAS 
    PubMed 
    Article 
    PubMed Central 

    Google Scholar
     

  • 39.

    Rolls, E. T., Treves, A., Robertson, R. G., Georges-François, P. & Panzeri, S. Information about spatial view in an ensemble of primate hippocampal cells. J. Neurophysiol. 79, 1797–1813 (1998).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 40.

    Miller, J. F. et al. Neural activity in human hippocampal formation reveals the spatial context of retrieved memories. Science 342, 1111–1114 (2013).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 41.

    Jacobs, J., Kahana, M. J., Ekstrom, A. D., Mollison, M. V. & Fried, I. A sense of direction in human entorhinal cortex. Proc. Natl Acad. Sci. USA 107, 6487–6492 (2010).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 42.

    Aronov, D. & Tank, D. W. Engagement of neural circuits underlying 2D spatial navigation in a rodent virtual reality system. Neuron 84, 442–456 (2014).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 43.

    Chen, G., King, J. A., Lu, Y., Cacucci, F. & Burgess, N. Spatial cell firing during virtual navigation of open arenas by head-restrained mice. eLife 7, e34789 (2018).

    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 44.

    Resnik, E., McFarland, J. M., Sprengel, R., Sakmann, B. & Mehta, M. R. The effects of GluA1 deletion on the hippocampal population code for position. J. Neurosci. 32, 8952–8968 (2012).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 45.

    Tse, D. et al. Schemas and memory consolidation. Science 316, 76–82 (2007).

    ADS 
    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 46.

    Rubin, A., Yartsev, M. M. & Ulanovsky, N. Encoding of head direction by hippocampal place cells in bats. J. Neurosci. 34, 1067–1080 (2014).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 47.

    Shahi, M. et al. A generalized linear model approach to dissociate object-centric and allocentric directional responses in hippocampal place cells. Soc. Neurosci. Abstr. 1, (2017).

  • 48.

    Jercog, P. E. et al. Heading direction with respect to a reference point modulates place-cell activity. Nat. Commun. 10, 2333 (2019).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 49.

    Cabral, H. O., Fouquet, C., Rondi-Reig, L., Pennartz, C. M. A. & Battaglia, F. P. Single-trial properties of place cells in control and CA1 NMDA receptor subunit 1-KO mice. J. Neurosci. 34, 15861–15869 (2014).

    PubMed 
    PubMed Central 
    Article 
    CAS 

    Google Scholar
     

  • 50.

    Mehta, M. R. Neuronal dynamics of predictive coding. Neurosci. 7, 490–495 (2001).

    CAS 

    Google Scholar
     

  • 51.

    Harvey, C. D., Collman, F., Dombeck, D. A. & Tank, D. W. Intracellular dynamics of hippocampal place cells during virtual navigation. Nature 461, 941–946 (2009).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 52.

    Safaryan, K. & Mehta, M. Enhanced hippocampal theta rhythmicity and emergence of eta oscillation in virtual reality. Nat. Neurosci. 24, 1065–1070 (2021).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 53.

    Kumar, A. & Mehta, M. R. Frequency-dependent changes in NMDAR-dependent synaptic plasticity. Front. Comput. Neurosci. 5, 38 (2011).

    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 54.

    Wang, S. H. & Morris, R. G. M. Hippocampal-neocortical interactions in memory formation, consolidation, and reconsolidation. Annu. Rev. Psychol. 61, 49–79 (2010).

    PubMed 
    Article 

    Google Scholar
     

  • 55.

    Mehta, M. R. Cortico-hippocampal interaction during up-down states and memory consolidation. Nat. Neurosci. 10, 13–15 (2007).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 56.

    Brun, V. H. et al. Place cells and place recognition maintained by direct entorhinal–hippocampal circuitry. Science 296, 2243–2246 (2002).

    ADS 
    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 57.

    Ahmed, O. J. & Mehta, M. R. The hippocampal rate code: anatomy, physiology and theory. Trends Neurosci. 32, 329–338 (2009).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 58.

    Mehta, M. R. Contribution of Ih to LTP, place cells, and grid cells. Cell 147, 968–970 (2011).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 59.

    Moore, J. J. et al. Dynamics of cortical dendritic membrane potential and spikes in freely behaving rats. Science 355, eaaj1497 (2017).

    PubMed 
    Article 
    CAS 

    Google Scholar
     

  • 60.

    Mehta, M. R. Cooperative LTP can map memory sequences on dendritic branches. Trends Neurosci. 27, 69–72 (2004).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 61.

    Wolbers, T., Wiener, J. M., Mallot, H. A. & Büchel, C. Differential recruitment of the hippocampus, medial prefrontal cortex, and the human motion complex during path integration in humans. J. Neurosci. 27, 9408–9416 (2007).

    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 62.

    Hahn, T. T. G., McFarland, J. M., Berberich, S., Sakmann, B. & Mehta, M. R. Spontaneous persistent activity in entorhinal cortex modulates cortico-hippocampal interaction in vivo. Nat. Neurosci. 15, 1531–1538 (2012).

    CAS 
    PubMed 
    Article 

    Google Scholar
     

  • 63.

    Wang, C. et al. Egocentric coding of external items in the lateral entorhinal cortex. Science 362, 945–949 (2018).

    ADS 
    CAS 
    PubMed 
    PubMed Central 
    Article 

    Google Scholar
     

  • 64.

    Friedman, J., Hastie, T. & Tibshirani, R. Regularized paths for generalized linear models via coordinate descent. J. Stat. Softw. 33, 1–22 (2008).


    Google Scholar
     

  • 65.

    Boyd, J. P. Chebyshev and Fourier Spectral Methods. 2nd revised edn (Dover Publications, 2000).

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