• Claire E Manning, Andrew L Eagle, Christine C Kwiatkowski, Ridouane Achargui, Hillary Woodworth, Emily Potter, Yoshinori Ohnishi, Gina M Leinninger, and A J Robison.
• Department of Physiology, Michigan State University, East Lansing, MI, USA 48824.
• Neuroscience. 2019 May 15; 406: 225-233.

AbstractNeural proliferation in the dentate gyrus (DG) is closely linked with learning and memory, but the transcriptional programming that drives adult proliferation remains incompletely understood. Our lab previously elucidated the critical role of the transcription factor ΔFosB in the dorsal hippocampus (dHPC) in learning and memory, and the FosB gene has been suggested to play a role in neuronal proliferation. However, the subregion-specific and potentially cell-autonomous role of dHPC ΔFosB in neurogenesis-dependent learning has not been studied. Here, we crossed neurotensin receptor-2 (NtsR2) Cre mice, which express Cre within the subgranular zone (SGZ) of dHPC DG, with floxed FosB mice to show that knockout of ΔFosB in hippocampal SGZ neurons reduces antidepressant-induced neurogenesis and impedes hippocampus-dependent learning in the novel object recognition task. Taken together, these data indicate that FosB gene expression in SGZ is necessary for both hippocampal neurogenesis and memory formation.Copyright © 2019 IBRO. Published by Elsevier Ltd. All rights reserved.

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