Hubel, D. H. & Wiesel, T. N. Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex. J. Physiol. 160, 106–154 (1962).
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).
O’Keefe, J. & Nadel, L. The Hippocampus as a Cognitive Map (Clarendon Press, 1978).
Muller, R. U. & Kubie, J. L. The firing of hippocampal place cells predicts the future position of freely moving rats. J. Neurosci. 9, 4101–4110 (1989).
Mehta, M. R. Neuronal dynamics of predictive coding. Neuroscience 7, 490–495 (2001).
Battaglia, F. P., Sutherland, G. R. & McNaughton, B. L. Local sensory cues and place cell directionality: additional evidence of prospective coding in the hippocampus. J. Neurosci. 24, 4541–4550 (2004).
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).
Ravassard, P. et al. Multisensory control of hippocampal spatiotemporal selectivity. Science 340, 1342–1346 (2013).
Aghajan, Z. M. et al. Impaired spatial selectivity and intact phase precession in two-dimensional virtual reality. Nat. Neurosci. 18, 121–128 (2015).
Pastalkova, E., Itskov, V., Amarasingham, A., Buzsaki, G. & Buzsáki, G. Internally generated cell assembly sequences in the rat hippocampus. Science 321, 1322–1327 (2008).
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).
Moore, J. J., Cushman, J. D., Acharya, L., Popeney, B. & Mehta, M. R. Linking hippocampal multiplexed tuning, Hebbian plasticity and navigation. Nature 599, 442–448 (2021).
Fyhn, M., Molden, S., Witter, M. P., Moser, E. I. & Moser, M. B. Spatial representation in the entorhinal cortex. Science 305, 1258–1264 (2004).
Taube, J. S., Muller, R. U. & Ranck, J. B. Jr Head-direction cells recorded from the postsubiculum in freely moving rats. II. Effects of environmental manipulations. J. Neurosci. 10, 436–447 (1990).
Foster, T. C., Castro, C. A. & McNaughton, B. L. Spatial selectivity of rat hippocampal neurons: dependence on preparedness for movement. Science 244, 1580–1582 (1989).
McNaughton, B. L. et al. Deciphering the hippocampal polyglot: the hippocampus as a path integration system. J. Exp. Biol. 199, 173–185 (1996).
Sakurai, Y. Involvement of auditory cortical and hippocampal neurons in auditory working memory and reference memory in the rat. J. Neurosci. 14, 2606–2623 (1994).
Itskov, P. M. et al. Sound sensitivity of neurons in rat hippocampus during performance of a sound-guided task sound sensitivity of neurons in rat hippocampus during performance of a sound-guided task. J. Neurophysiol. 107, 1822–1834 (2012).
Aronov, D., Nevers, R. & Tank, D. W. Mapping of a non-spatial dimension by the hippocampal–entorhinal circuit. Nature 543, 719–722 (2017).
Omer, D. B., Maimon, S. R., Las, L. & Ulanovsky, N. Social place-cells in the bat hippocampus. Science 359, 218–224 (2018).
Danjo, T., Toyoizumi, T. & Fujisawa, S. Spatial representations of self and other in the hippocampus. Science 359, 213–218 (2018).
von Heimendahl, M., Rao, R. P. & Brecht, M. Weak and nondiscriminative responses to conspecifics in the rat hippocampus. J. Neurosci. 32, 2129–2141 (2012).
Mou, X. & Ji, D. Social observation enhances cross-environment activation of hippocampal place cell patterns. eLife 5, 1–26 (2016).
Dotson, N. M. & Yartsev, M. M. Nonlocal spatiotemporal representation in the hippocampus of freely flying bats. Science 373, 242–247 (2021).
Sakurai, Y. Coding of auditory temporal and pitch information by hippocampal individual cells and cell assemblies in the rat. Neuroscience 115, 1153–1163 (2002).
Cushman, J. D. et al. Multisensory control of multimodal behavior: do the legs know what the tongue is doing? PLoS ONE 8, e80465 (2013).
Malpeli, J. G. & Baker, F. H. The representation of the visual field in the lateral geniculate nucleus of Macaca mulatta. J. Comp. Neurol. 161, 569–594 (1975).
Mehta, M. R., Quirk, M. C. & Wilson, M. A. Experience-dependent asymmetric shape of hippocampal receptive fields. Neuron 25, 707–715 (2000).
Ahmed, O. J. & Mehta, M. R. The hippocampal rate code: anatomy, physiology and theory. Trends Neurosci. 32, 329–338 (2009).
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).
de Vries, S. E. J. et al. A large-scale standardized physiological survey reveals functional organization of the mouse visual cortex. Nat. Neurosci. 23, 138–151 (2020).
Wilson, M. A. & McNaughton, B. L. Dynamics of the hippocampal ensemble code for space. Science 261, 1055–1058 (1993).
Stefanini, F. et al. A distributed neural code in the dentate gyrus and in CA1. Neuron 107, 703–716.e4 (2020).
Muller, R. U., Kubie, J. L., Bostock, E. M., Taube, J. S. & Quirk, G. J. in Brain and Space (ed. Paillard, J.) 296–333 (Oxford Univ. Press, 1991).
Colgin, L. L., Moser, E. I. & Moser, M. B. Understanding memory through hippocampal remapping. Trends Neurosci. 31, 469–477 (2008).
Suzuki, W. A., Miller, E. K. & Desimone, R. Object and place memory in the macaque entorhinal cortex. J. Neurophysiol. 78, 1062–1081 (1997).
Saleem, A. B., Diamanti, E. M., Fournier, J., Harris, K. D. & Carandini, M. Coherent encoding of subjective spatial position in visual cortex and hippocampus. Nature 562, 124–127 (2018).
Markus, E. J. et al. Interactions between location and task affect the spatial and directional firing of hippocampal neurons. J. Neurosci. 15, 7079–7094 (1995).
Ziv, Y. et al. Long-term dynamics of CA1 hippocampal place codes. Nat. Neurosci. 16, 264–266 (2013).
Nakazawa, K. et al. Requirement for hippocampal CA3 NMDA receptors in associative memory recall. Science 297, 211–218 (2002).
Geiller, T., Fattahi, M., Choi, J.-S. S. & Royer, S. Place cells are more strongly tied to landmarks in deep than in superficial CA1. Nat. Commun. 8, 14531 (2017).
Taube, J. S. & Muller, R. U. Comparisons of head direction cell activity in the postsubiculum and anterior thalamus of freely moving rats. Hippocampus 8, 87–108 (1998).
Deacon, T. W., Eichenbaum, H., Rosenberg, P. & Eckmann, K. W. Afferent connections of the perirhinal cortex in the rat. J. Comp. Neurol. 220, 168–190 (1983).
Lozano, Y. R. et al. Retrosplenial and postsubicular head direction cells compared during visual landmark discrimination. Brain Neurosci. Adv. 1, 2398212817721859 (2017).
Felleman, D. J. & Van Essen, D. C. Distributed hierarchical processing in the primate cerebral cortex. Cereb. Cortex 1, 1–47 (1991).
Hubel, D. H. & Wiesel, T. N. Receptive fields of single neurones in the cat’s striate cortex. J. Physiol. 148, 574–591 (1959).
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).
Quiroga, R. Q., Reddy, L., Kreiman, G., Koch, C. & Fried, I. Invariant visual representation by single neurons in the human brain. Nature 435, 1102–1107 (2005).
Hahn, T. T., Sakmann, B. & Mehta, M. R. Phase-locking of hippocampal interneurons’ membrane potential to neocortical up-down states. Nat. Neurosci. 9, 1359–1361 (2006).
Hahn, T. T., Sakmann, B. & Mehta, M. R. Differential responses of hippocampal subfields to cortical up-down states. Proc. Natl Acad. Sci. USA 104, 5169–5174 (2007).
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).
Beltramo, R. & Scanziani, M. A collicular visual cortex: neocortical space for an ancient midbrain visual structure. Science 363, 64–69 (2019).
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).
Berens, P. CircStat: a MATLAB toolbox for circular statistics. J. Stat. Softw. 31, 1–21 (2009).
Ringach, D. L., Shapley, R. M. & Hawken, M. J. Orientation selectivity in macaque V1: diversity and laminar dependence. J. Neurosci. 22, 5639–5651 (2002).
Ghodrati, M., Zavitz, E., Rosa, M. G. P. & Price, N. S. C. Contrast and luminance adaptation alter neuronal coding and perception of stimulus orientation. Nat. Commun. 10, 941 (2019).
More News
Editorial Expression of Concern: Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase – Nature
Quantum control of a cat qubit with bit-flip times exceeding ten seconds – Nature
Venus water loss is dominated by HCO+ dissociative recombination – Nature