Postnatal development of pre- and postsynaptic GABA markers at chandelier cell connections with pyramidal neurons in monkey prefrontal cortex
Article first published online: 3 SEP 2003
Copyright © 2003 Wiley-Liss, Inc.
Journal of Comparative Neurology
Volume 465, Issue 3, pages 385–400, 20 October 2003
How to Cite
Cruz, D. A., Eggan, S. M. and Lewis, D. A. (2003), Postnatal development of pre- and postsynaptic GABA markers at chandelier cell connections with pyramidal neurons in monkey prefrontal cortex. J. Comp. Neurol., 465: 385–400. doi: 10.1002/cne.10833
- Issue published online: 3 SEP 2003
- Article first published online: 3 SEP 2003
- Manuscript Accepted: 19 MAY 2003
- Manuscript Revised: 15 MAY 2003
- Manuscript Received: 12 MAR 2003
- U.S. Public Health Service. Grant Numbers: MH45156, MH43784
- GABA transporters;
- GABAA receptors
The protracted postnatal maturation of the primate prefrontal cortex (PFC) is associated with substantial changes in the number of excitatory synapses on pyramidal neurons, whereas the total number of inhibitory synapses appears to remain constant. In this study, we sought to determine whether the developmental changes in excitatory input to pyramidal cells are paralleled by changes in functional markers of inhibitory inputs to pyramidal neurons. The chandelier subclass of γ-aminobutyric acid (GABA) neurons provides potent inhibitory control over pyramidal neurons by virtue of their axon terminals, which form distinct vertical structures (termed cartridges) that synapse at the axon initial segment (AIS) of pyramidal neurons. Thus, we examined the relative densities, laminar distributions, and lengths of presynaptic chandelier axon cartridges immunoreactive for the GABA membrane transporter 1 (GAT1) or the calcium-binding protein parvalbumin (PV) and of postsynaptic pyramidal neuron AIS immunoreactive for the GABAA receptor α2 subunit (GABAA α2) in PFC area 46 of 38 rhesus monkeys (Macaca mulatta). From birth through 2 years of age, the relative densities and laminar distributions of these three markers exhibited different trajectories, suggesting developmental shifts in the weighting of at least some factors that determine inhibition at the AIS. In contrast, from 2 to 4 years of age, all three markers exhibited similar declines in density and length that paralleled the periadolescent pruning of excitatory synapses to pyramidal neurons. Across development, the predominant laminar location of PV-labeled cartridges and GABAA α2-immunoreactive AIS shifted from the middle to superficial layers, whereas the laminar distribution of GAT1-positive cartridges did not change. Together, these findings suggest that the maturation of inhibitory inputs to the AIS of PFC pyramidal neurons is a complex process that may differentially affect the firing patterns of subpopulations of pyramidal neurons at specific postnatal time points. J. Comp. Neurol. 465:385–400, 2003. © 2003 Wiley-Liss, Inc.