Journal
MOLECULAR PSYCHIATRY
Volume 26, Issue 1, Pages 350-364Publisher
SPRINGERNATURE
DOI: 10.1038/s41380-019-0598-7
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Funding
- Intramural NIH HHS [ZIA ES100221-17, Z01 ES100221] Funding Source: Medline
- NIMH NIH HHS [R00 MH109626, K99 MH109626] Funding Source: Medline
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Mineralocorticoid receptors in the brain, specifically in the CA2 region of the hippocampus, play a crucial role in regulating neuronal properties and behaviors associated with CA2. Experiments showed that modulation of MRs affected molecular markers, synaptic inputs, synaptic currents, social behavior, and responses to novelty in CA2.
Mineralocorticoid receptors (MRs) in the brain play a role in learning and memory, neuronal differentiation, and regulation of the stress response. Within the hippocampus, the highest expression of MRs is in area CA2. CA2 pyramidal neurons have a distinct molecular makeup resulting in a plasticity-resistant phenotype, distinguishing them from neurons in CA1 and CA3. Thus, we asked whether MRs regulate CA2 neuron properties and CA2-related behaviors. Using three conditional knockout methods at different stages of development, we found a striking decrease in multiple molecular markers for CA2, an effect mimicked by chronic antagonism of MRs. Furthermore, embryonic deletion of MRs disrupted afferent inputs to CA2 and enabled synaptic potentiation of the normally LTP-resistant synaptic currents in CA2. We also found that CA2-targeted MR knockout was sufficient to disrupt social behavior and alter behavioral responses to novelty. Altogether, these results demonstrate an unappreciated role for MRs in controlling CA2 pyramidal cell identity and in facilitating CA2-dependent behaviors.
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