Ventral hippocampal projections to the medial prefrontal cortex regulate social memory

Autor: Holly Anne Robinson, Lucas Pozzo-Miller, Mary L. Phillips
Jazyk: angličtina
Rok vydání: 2018
Předmět:
0301 basic medicine
Social memory
social memory
Mouse
Autism Spectrum Disorder
Hippocampus
Hippocampal formation
Mice
0302 clinical medicine
Rett syndrome
Biology (General)
Prefrontal cortex
0303 health sciences
Behavior
Animal

General Neuroscience
Pyramidal Cells
musculoskeletal
neural
and ocular physiology

General Medicine
Temporal Lobe
Autism spectrum disorder
Knockout mouse
behavior and behavior mechanisms
Medicine
psychological phenomena and processes
Research Article
QH301-705.5
Science
Prefrontal Cortex
autism
Biology
behavioral disciplines and activities
General Biochemistry
Genetics and Molecular Biology

MECP2
03 medical and health sciences
Memory
medicine
Animals
Humans
Mecp2
030304 developmental biology
General Immunology and Microbiology
Recall
medicine.disease
030104 developmental biology
nervous system
Autism
Neuroscience
ventral hippocampus
030217 neurology & neurosurgery
medial prefrontal cortex
Zdroj: eLife
eLife, Vol 8 (2019)
DOI: 10.1101/461533
Popis: SUMMARYInputs from the ventral hippocampus (vHIP) to the medial prefrontal cortex (mPFC) have been implicated in several neuropsychiatric disorders. Here, we show that the long-range vHIP-mPFC projection is hyperactive in the Mecp2 knockout (KO) mouse model of the autism spectrum disorder Rett syndrome, which has deficits in social memory. Chronically mimicking vHIP-mPFC hyperexcitability in wild-type mice impaired social memory, whereas chronic inhibition of mPFC-projecting vHIP neurons in Mecp2 KO mice rescued social memory deficits; the extent of memory rescue was negatively correlated with the strength of vHIP input to the mPFC. Acute manipulations of the vHIP-mPFC projection also affected social memory in a specific and selective manner, suggesting that proper vHIP-mPFC signaling is necessary to recall social memories. In addition, we identified an altered vHIP-mPFC innervation pattern and increased synaptic strength onto layer 5 pyramidal neurons as contributing factors in aberrant vHIP-mPFC signaling in Mecp2 KO mice.
Databáze: OpenAIRE