Chandelier cells control excessive cortical excitation: Characteristics of whisker-evoked synaptic responses of layer 2/3 nonpyramidal and pyramidal neurons

被引:102
|
作者
Zhu, YH
Stornetta, RL
Zhu, JJ
机构
[1] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[3] Max Planck Inst Med Res, Dept Cell Physiol, D-69120 Heidelberg, Germany
来源
JOURNAL OF NEUROSCIENCE | 2004年 / 24卷 / 22期
关键词
rat; somatosensory; excitation; inhibition; whisker; epilepsy;
D O I
10.1523/JNEUROSCI.0544-04.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chandelier cells form inhibitory axo-axonic synapses on pyramidal neurons with their characteristic candlestick-like axonal terminals. The functional role of chandelier cells is still unclear, although the preferential loss of this cell type at epileptic loci suggests a role in epilepsy. Here we report an examination of whisker-and spontaneous activity-evoked responses in chandelier cells and other fast-spiking nonpyramidal neurons and regular-spiking pyramidal neurons in layer 2/3 of the barrel cortex. Fast-spiking nonpyramidal neurons, including chandelier cells, basket cells, neurogliaform cells, double bouquet cells, net basket cells, bitufted cells, and regular-spiking pyramidal neurons all respond to stimulation of multiple whiskers on the contralateral face. Whisker stimulation, however, evokes small, delayed EPSPs preceded by an earlier IPSP and no action potentials in chandelier cells, different from other nonpyramidal and pyramidal neurons. In addition, chandelier cells display a larger receptive field with lower acuity than other fast-spiking nonpyramidal neurons and pyramidal neurons. Notably, simultaneous dual whole-cell in vivo recordings show that chandelier cells, which rarely fire action potentials spontaneously, fire more robustly than other types of cortical neurons when the overall cortical excitation increases. Thus, chandelier cells may not process fast ascending sensory information but instead may be reserved to prevent excessive excitatory activity in neuronal networks.
引用
收藏
页码:5101 / 5108
页数:8
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