| First Author | Chen S | Year | 2020 |
| Journal | Nature | Volume | 586 |
| Issue | 7828 | Pages | 270-274 |
| PubMed ID | 32999460 | Mgi Jnum | J:297389 |
| Mgi Id | MGI:6472570 | Doi | 10.1038/s41586-020-2771-1 |
| Citation | Chen S, et al. (2020) A hypothalamic novelty signal modulates hippocampal memory. Nature 586(7828):270-274 |
| abstractText | The ability to recognize information that is incongruous with previous experience is critical for survival. Novelty signals have therefore evolved in the mammalian brain to enhance attention, perception and memory(1,2). Although the importance of regions such as the ventral tegmental area(3,4) and locus coeruleus(5) in broadly signalling novelty is well-established, these diffuse monoaminergic transmitters have yet to be shown to convey specific information on the type of stimuli that drive them. Whether distinct types of novelty, such as contextual and social novelty, are differently processed and routed in the brain is unknown. Here we identify the supramammillary nucleus (SuM) as a novelty hub in the hypothalamus(6). The SuM region is unique in that it not only responds broadly to novel stimuli, but also segregates and selectively routes different types of information to discrete cortical targets-the dentate gyrus and CA2 fields of the hippocampus-for the modulation of mnemonic processing. Using a new transgenic mouse line, SuM-Cre, we found that SuM neurons that project to the dentate gyrus are activated by contextual novelty, whereas the SuM-CA2 circuit is preferentially activated by novel social encounters. Circuit-based manipulation showed that divergent novelty channelling in these projections modifies hippocampal contextual or social memory. This content-specific routing of novelty signals represents a previously unknown mechanism that enables the hypothalamus to flexibly modulate select components of cognition. |
