학술논문

Alterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors
Document Type
Report
Author abstract
Source
Proceedings of the National Academy of Sciences of the United States. June 22, 2010, Vol. 107 Issue 25, p11567, 6 p.
Subject
United States
Language
English
ISSN
0027-8424
Abstract
The neuronal nicotinic acetylcholine receptors (nAChRs) are allosteric membrane proteins involved in multiple cognitive processes, including attention, learning, and memory. The most abundant form of heterooligomeric nAChRs in the brain contains the [beta]2- and [alpha]4- subunits and binds nicotinic agonists with high affinity. In the present study, we investigated in the mouse the consequences of the deletion of one of the nAChR components: the [beta]2-subunit ([[beta]2.sup.-/-]) on the microanatomy of cortical pyramidal cells. Using an intracellular injection method, complete basal dendritic arbors of 650 layer III pyramidal neurons were sampled from seven cortical fields, including primary sensory, motor, and associational areas, in both [[beta].sup.-/-] and WT animals. We observed that the pyramidal cell phenotype shows significant quantitative differences among different cortical areas in mutant and WT mice. In WT mice, the density of dendritic spines was rather similar in all cortical fields, except in the prelimbic/infralimbic cortex, where it was significantly higher. In the absence of the [beta]2-subunit, the most significant reduction in the density of spines took place in this high-order associational field. Our data suggest that the [beta]2-subunit is involved in the dendritic morphogenesis of pyramidal neurons and, in particular, in the circuits that contribute to the high-order functional connectivity of the cerebral cortex. cerebral cortex | dendrites | dendritic spines | long-range connections | global neuronal workspace doi/ 10.1073/pnas.1006269107