Early life adversity shapes social subordination and cell type-specific transcriptomic patterning in the ventral hippocampus.
Aron KosJuan Pablo LopezJoeri BordesCarlo de DonnoJulien DineElena BrivioStoyo KaramihalevMalte Daniel LueckenSuellen Almeida-CorreaSerena GasperoniAlec DickLucas MirandaMaren BüttnerRainer StoffelCornelia FlachskammFabian Joachim TheisMathias V SchmidtAlon ChenPublished in: Science advances (2023)
Adverse events in early life can modulate the response to additional stressors later in life and increase the risk of developing psychiatric disorders. The underlying molecular mechanisms responsible for these effects remain unclear. Here, we uncover that early life adversity (ELA) in mice leads to social subordination. Using single-cell RNA sequencing (scRNA-seq), we identified cell type-specific changes in the transcriptional state of glutamatergic and GABAergic neurons in the ventral hippocampus of ELA mice after exposure to acute social stress in adulthood. These findings were reflected by an alteration in excitatory and inhibitory synaptic transmission induced by ELA in response to acute social stress. Finally, enhancing the inhibitory network function through transient diazepam treatment during an early developmental sensitive period reversed the ELA-induced social subordination. Collectively, this study significantly advances our understanding of the molecular, physiological, and behavioral alterations induced by ELA, uncovering a previously unknown cell type-specific vulnerability to ELA.
Keyphrases
- early life
- single cell
- healthcare
- mental health
- rna seq
- liver failure
- spinal cord
- prefrontal cortex
- drug induced
- respiratory failure
- deep brain stimulation
- adipose tissue
- high fat diet induced
- high throughput
- cerebral ischemia
- metabolic syndrome
- transcription factor
- cognitive impairment
- aortic dissection
- intensive care unit
- oxidative stress
- heat stress
- endothelial cells
- heat shock