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Dendritic Discrimination of Temporal Input Sequences in Cortical Neurons

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Journal Science
Specialty Science
Date 2010 Aug 14
PMID 20705816
Citations 209
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Abstract

The detection and discrimination of temporal sequences is fundamental to brain function and underlies perception, cognition, and motor output. By applying patterned, two-photon glutamate uncaging, we found that single dendrites of cortical pyramidal neurons exhibit sensitivity to the sequence of synaptic activation. This sensitivity is encoded by both local dendritic calcium signals and somatic depolarization, leading to sequence-selective spike output. The mechanism involves dendritic impedance gradients and nonlinear synaptic N-methyl-D-aspartate receptor activation and is generalizable to dendrites in different neuronal types. This enables discrimination of patterns delivered to a single dendrite, as well as patterns distributed randomly across the dendritic tree. Pyramidal cell dendrites can thus act as processing compartments for the detection of synaptic sequences, thereby implementing a fundamental cortical computation.

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References
1.
Euler T, Detwiler P, Denk W . Directionally selective calcium signals in dendrites of starburst amacrine cells. Nature. 2002; 418(6900):845-52. DOI: 10.1038/nature00931. View

2.
Mel B . Synaptic integration in an excitable dendritic tree. J Neurophysiol. 1993; 70(3):1086-101. DOI: 10.1152/jn.1993.70.3.1086. View

3.
Han F, Caporale N, Dan Y . Reverberation of recent visual experience in spontaneous cortical waves. Neuron. 2008; 60(2):321-7. PMC: 3576032. DOI: 10.1016/j.neuron.2008.08.026. View

4.
Losonczy A, Magee J . Integrative properties of radial oblique dendrites in hippocampal CA1 pyramidal neurons. Neuron. 2006; 50(2):291-307. DOI: 10.1016/j.neuron.2006.03.016. View

5.
Wehr M, Laurent G . Odour encoding by temporal sequences of firing in oscillating neural assemblies. Nature. 1996; 384(6605):162-6. DOI: 10.1038/384162a0. View