Cargando…

Nicotinic regulation of local and long-range input balance drives top-down attentional circuit maturation

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 proje...

Descripción completa

Detalles Bibliográficos
Autores principales: Falk, Elisa N., Norman, Kevin J., Garkun, Yury, Demars, Michael P., Im, Susanna, Taccheri, Giulia, Short, Jenna, Caro, Keaven, McCraney, Sarah E., Cho, Christina, Smith, Milo R., Lin, Hung-Mo, Koike, Hiroyuki, Bateh, Julia, Maccario, Priscilla, Waltrip, Leah, Janis, Meaghan, Morishita, Hirofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935362/
https://www.ncbi.nlm.nih.gov/pubmed/33674307
http://dx.doi.org/10.1126/sciadv.abe1527
Descripción
Sumario: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.