Abstract
Corticotropin-releasing hormone (CRH) signaling in the hippocampus has been established to be important for mediating the effects of stress on learning and memory. Given our laboratory’s recent characterization of a subset of hippocampal CRH neurons as a novel class of GABAergic interneurons, we hypothesized that these local GABAergic hippocampal CRH neurons may influence hippocampal function. Here we applied an array of molecular tools to selectively label and manipulate hippocampal CRH neurons in mice, in order to assess this interneuron population’s impact on hippocampus-dependent behaviors and hippocampal network excitability. Genetically-targeted ablation of hippocampal CRH neurons in vivo impaired object recognition memory and substantially enhanced the severity of kainic acid-induced seizures. Conversely, selective activation of CRH neurons in vitro suppressed the excitability of the mossy fiber-CA3 pathway. Additional experiments are needed to reconcile the functions of GABA and CRH signaling of hippocampal CRH neurons on hippocampal function. However, our results indicate that this interneuron population plays an important role in maintaining adaptive network excitability, and provide a specific circuit-level mechanism for this role.
Highlights
The hippocampus is critical for spatial navigation and episodic memory formation [1, 2]
The bacterial artificial chromosome (BAC) Corticotropin-releasing hormone (CRH)-Cre mouse is a useful tool for manipulating a subset of hippocampal CRH neurons
In order to determine whether the BAC CRH-Cre line faithfully targets Cre expression to bona fide hippocampal CRH neurons, we assessed CRH reporter expression and its colocalization with CRH peptide immunoreactivity in BAC CRH-Cre/Ai9 and CRH-iresCre/Ai9 hippocampal sections
Summary
The hippocampus is critical for spatial navigation and episodic memory formation [1, 2] Both of these tasks require precisely timed synchronous output, which is accomplished by over 20 distinct classes of hippocampal GABAergic interneurons [3, 4]. This must be done while clamping the overall excitability and synchrony of the hippocampus within an adaptive range, in order to avoid runaway excitation lead to an epileptic seizure, a pathological state of hypersynchronous hyperexcitability to which the hippocampus is vulnerable [5, 6].
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