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Nicotinic regulation of local and long-range input balance drives top-down attentional circuit maturation
- Source :
- Science Advances
- Publication Year :
- 2021
- Publisher :
- American Association for the Advancement of Science, 2021.
-
Abstract
- Nicotinic signaling regulates top-down circuit maturation and restores attention deficits in mouse model of fragile X syndrome.<br />Cognitive function depends on frontal cortex development; however, the mechanisms driving this process are poorly understood. Here, we identify that dynamic regulation of the nicotinic cholinergic system is a key driver of attentional circuit maturation associated with top-down frontal neurons projecting to visual cortex. The top-down neurons receive robust cholinergic inputs, but their nicotinic tone decreases following adolescence by increasing expression of a nicotinic brake, Lynx1. Lynx1 shifts a balance between local and long-range inputs onto top-down frontal neurons following adolescence and promotes the establishment of attentional behavior in adulthood. This key maturational process is disrupted in a mouse model of fragile X syndrome but was rescued by a suppression of nicotinic tone through the introduction of Lynx1 in top-down projections. Nicotinic signaling may serve as a target to rebalance local/long-range balance and treat cognitive deficits in neurodevelopmental disorders.
- Subjects :
- Nicotine
Frontal cortex
Cholinergic Agents
Biology
03 medical and health sciences
Mice
0302 clinical medicine
Developmental Neuroscience
LYNX1
medicine
Animals
Attention
Research Articles
030304 developmental biology
Balance (ability)
Visual Cortex
Neurons
0303 health sciences
Multidisciplinary
SciAdv r-articles
Cognition
medicine.disease
Fragile X syndrome
Nicotinic agonist
Visual cortex
medicine.anatomical_structure
Cholinergic
Neuroscience
030217 neurology & neurosurgery
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 23752548
- Volume :
- 7
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- Science Advances
- Accession number :
- edsair.doi.dedup.....764ea546930993eb624465cebd5afa74