Place Cells and Place Recognition Maintained by Direct Entorhinal-Hippocampal Circuitry

By V. H. Brun, Mona K. Otnæss, S. Molden, H. Steffenach, Menno P. Witter, May-Britt Moser, Edvard I. Moser. Science, 2002

619 citations recorded by the source corpus.

Subfields: Cell Biology, Cellular and Molecular Neuroscience, Cognitive Neuroscience

View Paper: https://www.semanticscholar.org/paper/7108582228996d44ac36fda40ca18622ca158b46

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Citations in the corpus

Remembering the past and imagining the future (2007, neutral): “In our model, this recurrent connectivity allows for recall/pattern completion, as it is often argued to do in CA3 (Brun et al., 2002; Nakazawa et al., 2002).”
Progressive transformation of hippocampal neuronal representations in "morphed" environments. (2005, background): “However, nonlinear response patterns in CA1 may also reflect output from attractor networks in the neocortex (Hafting et al., 2005), which may influence place cells through direct connections from the entorhinal cortex (Brun et al., 2002).”
Modes and Models of Forebrain Cholinergic Neuromodulation of Cognition (2010, background): “Such local control of cholinergic activity may imply that the cholinergic system influences target regions in a more specific manner than previously assumed.”
A Spin Glass Model of Path Integration in Rat Medial Entorhinal Cortex (2006, background): “Place fields in CA1 are observed even when the Schaffer collateral projection from CA3 is severed (Brun et al., 2002).”
Impaired spatial representation in CA1 after lesion of direct input from entorhinal cortex. (2008, background): “Localized firing is maintained after selective disruption of all input from CA3 (Brun et al., 2002) as well as after reduced transmission through the indirect pathway by selective lesions of the dentate gyrus (McNaughton et al.”
Pattern separation, completion, and categorisation in the hippocampus and neocortex. (2016, background): “…is not necessarily required during recall in a reference memory spatial task, such as the water maze spatial navigation for a single spatial location task, is that CA3 lesioned rats are not impaired during recall of a previously learned water maze task (Brun et al., 2002; Florian & Roullet, 2004).”
Elements of a neurobiological theory of hippocampal function: the role of synaptic plasticity, synaptic tagging and schemas (2006, methodology): “Indeed, the internal recurrent connectivity of hippocampal area CA3 makes the region highly suitable for storage of just this type of patterned information, at least for an intermediate period of time and possibly for longer (Abraham et al., 2002).”
Hippocampal mechanisms for the context-dependent retrieval of episodes (2005, positive): “735 736 737 738 739 740 741 742 743 744 data showing that cutting the input from CA3 to CA1 does not impair recognition, but does impair selective recall (Brun et al., 2002).”
Differential control of learning and anxiety along the dorso-ventral axis of the dentate gyrus (2013, background): “In addition, our manipulations are specific to DG GCs, which leaves open the possibility that other areas of ventral hippocampus, most notably vCA1, may contribute to contextual fear conditioning or unconditioned anxiety.”