R. Boyce, S. Glasgow, S. Williams, and A. Adamantidis, Causal evidence for the role of REM sleep theta rhythm in contextual memory consolidation, Science, vol.352, issue.6287, pp.812-816, 2016.
DOI : 10.1126/science.aad5252

C. Denny, Hippocampal Memory Traces Are Differentially Modulated by Experience, Time, and Adult Neurogenesis, Neuron, vol.83, issue.1, pp.189-201, 2014.
DOI : 10.1016/j.neuron.2014.05.018

O. Gandrillon, F. Solari, C. Legrand, P. Jurdic, and J. Samarut, A rapid and convenient method to prepare DIG-labelled RNA probes for use in non-radioactivein situhybridization, Molecular and Cellular Probes, vol.10, issue.1, pp.51-55, 1996.
DOI : 10.1006/mcpr.1996.0007

M. Jouvet, F. Michel, and J. Courjon, Sur un stade d'activité e ´lectrique cérébrale rapide au cours du sommeil physiologique, CR Seances Soc Biol, vol.153, pp.1024-1028, 1959.

M. Kheirbek, Differential Control of Learning and Anxiety along the Dorsoventral Axis of the Dentate Gyrus, Neuron, vol.77, issue.5, pp.955-968, 2013.
DOI : 10.1016/j.neuron.2012.12.038

J. Kiss, A. Csaki, H. Bokor, M. Shanabrough, and C. Leranth, The supramammillo-hippocampal and supramammillo-septal glutamatergic/aspartatergic projections in the rat: a combined [3H]d-aspartate autoradiographic and immunohistochemical study, Neuroscience, vol.97, issue.4, pp.657-669, 2000.
DOI : 10.1016/S0306-4522(00)00127-5

L. Lerea and J. Mcnamara, Ionotropic glutamate receptor subtypes activate c-fos transcription by distinct calcium-requiring intracellular signaling pathways, Neuron, vol.10, issue.1, pp.31-41, 1993.
DOI : 10.1016/0896-6273(93)90239-N

X. Liu, S. Ramirez, P. Pang, C. Puryear, A. Govindarajan et al., Optogenetic stimulation of a hippocampal engram activates fear memory recall, Nature, vol.390, pp.381-38510, 1038.
DOI : 10.1038/nature11028

T. Mchugh, Dentate Gyrus NMDA Receptors Mediate Rapid Pattern Separation in the Hippocampal Network, Science, vol.317, issue.5834, pp.94-99, 2007.
DOI : 10.1126/science.1140263

S. Montgomery, A. Sirota, and G. Buzsaki, Theta and Gamma Coordination of Hippocampal Networks during Waking and Rapid Eye Movement Sleep, Journal of Neuroscience, vol.28, issue.26, pp.6731-6741, 2008.
DOI : 10.1523/JNEUROSCI.1227-08.2008

J. Neunuebel and J. Knierim, Spatial Firing Correlates of Physiologically Distinct Cell Types of the Rat Dentate Gyrus, Journal of Neuroscience, vol.32, issue.11, pp.3848-3858, 2012.
DOI : 10.1523/JNEUROSCI.6038-11.2012

S. Ohara, S. Sato, K. Tsutsui, M. Witter, and T. Iijima, Organization of Multisynaptic Inputs to the Dorsal and Ventral Dentate Gyrus: Retrograde Trans-Synaptic Tracing with Rabies Virus Vector in the Rat, PLoS ONE, vol.9, issue.11, 2013.
DOI : 10.1371/journal.pone.0078928.g012

P. Ravassard, REM Sleep-Dependent Bidirectional Regulation of Hippocampal-Based Emotional Memory and LTP, Cerebral Cortex, vol.26, issue.4, 2016.
DOI : 10.1093/cercor/bhu310

L. Renouard, The supramammillary nucleus and the claustrum activate the cortex during REM sleep, Science Advances, vol.1, issue.3, 2015.
DOI : 10.1126/sciadv.1400177

E. Sapin, Localization of the Brainstem GABAergic Neurons Controlling Paradoxical (REM) Sleep, PLoS ONE, vol.153, issue.1, 2009.
DOI : 10.1371/journal.pone.0004272.s006

E. Sapin, A. Berod, L. Leger, P. Herman, P. Luppi et al., A Very Large Number of GABAergic Neurons Are Activated in the Tuberal Hypothalamus during Paradoxical (REM) Sleep Hypersomnia, PLoS ONE, vol.556, issue.7, 2010.
DOI : 10.1371/journal.pone.0011766.t003

B. Schmidt, D. Marrone, and E. Markus, Disambiguating the similar: The dentate gyrus and pattern separation, Behavioural Brain Research, vol.226, issue.1, pp.56-65, 2012.
DOI : 10.1016/j.bbr.2011.08.039

R. Soussi, N. Zhang, S. Tahtakran, C. Houser, and M. Esclapez, Heterogeneity of the supramammillary-hippocampal pathways: evidence for a unique GABAergic neurotransmitter phenotype and regional differences, European Journal of Neuroscience, vol.405, issue.1-3, pp.771-785, 2010.
DOI : 10.1111/j.1460-9568.2010.07329.x

L. Swanson, Brain maps: structure of the rat brain A role of melanin-concentrating hormone producing neurons in the central regulation of paradoxical sleep, BMC Neurosci, vol.4, p.19, 1992.

R. Vertes, PHA-L analysis of projections from the supramammillary nucleus in the rat, The Journal of Comparative Neurology, vol.1, issue.4, pp.595-622, 1992.
DOI : 10.1002/cne.903260408

F. Wouterlood, Origin of calretinin-containing, vesicular glutamate transporter 2-coexpressing fiber terminals in the entorhinal cortex of the rat, The Journal of Comparative Neurology, vol.22, issue.2, pp.359-370, 2008.
DOI : 10.1002/cne.21555

L. Yassin, B. Benedetti, J. Jouhanneau, J. Wen, J. Poulet et al., An Embedded Subnetwork of Highly Active Neurons in the Neocortex, Neuron, vol.68, issue.6, 2010.
DOI : 10.1016/j.neuron.2010.11.029

. Fig, 5 FOS? neurons projecting to the vDG in PSR animals are mostly located in the medial entorhinal cortex. a, c, e Schematic distribution of singly FOS? (black dots), singly FG? (green dots), and FOS-FG double-labelled (red squares) neurons in the medial septum (a), the Sum (c), and the entorhinal cortex (e) in a representative PSR animal. b, d, f Photomicrographs showing FOS (black nuclear staining) and FG (brown cytoplasmatic staining) double-stained neurons in the medial septum, the Sum (d), and the entorhinal cortex (f) of a PSR rat. Note the dense cluster of doublelabelled neurons in the medial entorhinal cortex