Neuronal activity‐related transcription is blunted in immature compared to mature dentate granule cells
Year: 2023
Type: article
Abstract: Immature dentate granule cells (DGCs) generated in the hippocampus during adulthood are believed to play a unique role in dentate gyrus (DG) function. Although immature DGCs have hyperexcitable membrane properties in vitro, the consequences of this hyperexcitability in vivo remain unclear. In particular, the relationship between experiences that activate the DG, such as exploration of a novel environment (NE), and downstream molecular processes that modify DG circuitry in response to cellular activation is unknown in this cell population. We first performed quantification of immediate early gene (IEG) proteins in immature (5-week-old) and mature (13-week-old) DGCs from mice exposed to a NE. Paradoxically, we observed lower IEG protein expression in hyperexcitable immature DGCs. We then isolated nuclei from active and inactive immature DGCs and performed single-nuclei RNA-Sequencing. Compared to mature nuclei collected from the same animal, immature DGC nuclei showed less activity-induced transcriptional change, even though they were classified as active based on expression of ARC protein. These results demonstrate that the coupling of spatial exploration, cellular activation, and transcriptional change differs between immature and mature DGCs, with blunted activity-induced changes in immature cells.
Source: Hippocampus
DOI: 10.1002/hipo.23515
Institution: Salk Institute for Biological Studies
Language: English
Subfield: Developmental Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
Funders: American Heart Association, Brinson Foundation, Mary K. Chapman Foundation, Leona M. and Harry B. Helmsley Charitable Trust, JPB Foundation, Waitt Foundation, Paul G. Allen Frontiers Group, National Institutes of Health, National Institute on Aging, National Institute of Mental Health, National Cancer Institute
Awards: G4066625888, G4801963049, G6494258657, G7090803003, Understanding the cell biological drivers of aging as risk factors for cognitive impairment, UCSD Shiley-Marcos Alzheimer's Disease Research Center P30, Dynamics of activity-induced transcription in single dentate granule cells, Cancer Center Support Grant (CCSG)
OpenAlex ID: W4321496331
