Journal
JOURNAL OF NEUROSCIENCE
Volume 41, Issue 11, Pages 2475-2495Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1724-20.2021
Keywords
contextual fear conditioning; hilus; immediate early gene; memory; novelty; object recognition
Categories
Funding
- National Institutes of Health [R01 MH-109305]
- Natural Sciences and Engineering Research Council of Canada
- New York State Office of Mental Health
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The dentate gyrus (DG) of the hippocampus plays a crucial role in cognition and behavior, with mossy cells (MCs) potentially regulating anxiety-like behaviors and cognitive performance in specific ways. Manipulations of MCs can bidirectionally influence behaviors by activating or inhibiting MCs. Sex-specific effects were observed in some behaviors, with females showing more pronounced effects than males.
The dentate gyrus (DG) has many important cognitive roles as well as being associated with affective behavior. This study addressed how a glutamatergic DG cell type called mossy cells (MCs) contributes to diverse behaviors, which is timely because it is known that MCs regulate the activity of the primary DG cell type, granule cells (GCs), but how MC activity influences behavior is unclear. We show, surprisingly, that activating MCs can lead to adverse behavioral outcomes, and inhibiting MCs The dentate gyrus (DG) of the hippocampus is important for cognition and behavior. However, the circuits underlying these functions are unclear. DG mossy cells (MCs) are potentially important because of their excitatory synapses on the primary cell type, granule cells (GCs). However, MCs also activate GABAergic neurons, which inhibit GCs. We used viral delivery of designer receptors exclusively activated by designer drugs (DREADDs) in mice to implement a gain-and loss-of-function study of MCs in diverse behaviors. Using this approach, manipulations of MCs could bidirectionally regulate behavior. The results suggest that inhibiting MCs can reduce anxiety-like behavior and improve cognitive performance. However, not all cognitive or anxiety-related behaviors were influenced, suggesting specific roles of MCs in some, but not all, types of cognition and anxiety. Notably, several behaviors showed sex-specific effects, with females often showing more pronounced effects than the males. We also used the immediate early gene c-Fos to address whether DREADDs bidirectionally regulated MC or GC activity. We confirmed excitatory DREADDs increased MC c-Fos. However, there was no change in GC c-Fos, consistent with MC activation leading to GABAergic inhibition of GCs. In contrast, inhibitory DREADDs led to a large increase in GC c-Fos, consistent with a reduction in MC excitation of GABAergic neurons, and reduced inhibition of GCs. Together, these results suggest that MCs regulate anxiety and cognition in specific ways. We also raise the possibility that cognitive performance may be improved by reducing anxiety.
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