Properties of Piriform Cortex Pyramidal Cell Dendrites: Implications for Olfactory Circuit Design

被引:37
作者
Bathellier, Brice [1 ]
Margrie, Troy W. [2 ]
Larkum, Matthew E. [1 ]
机构
[1] Univ Bern, Dept Physiol, CH-3012 Bern, Switzerland
[2] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
基金
英国惠康基金; 瑞士国家科学基金会;
关键词
NEURONS IN-VITRO; ACTION-POTENTIAL BACKPROPAGATION; DEPENDENT SYNAPTIC PLASTICITY; BASAL DENDRITES; HIPPOCAMPAL-NEURONS; ONE BRANCH; INTEGRATION; SYNAPSES; BULB; HYPERPOLARIZATION;
D O I
10.1523/JNEUROSCI.1124-09.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Unlike the neocortex, sensory input to the piriform cortex is anatomically segregated in layer 1, making it ideal for studying the dendritic integration of synaptic inputs pivotal for sensory information processing. Here we investigated dendritic integration of olfactory bulb inputs in pyramidal cells using dual patch-clamp recordings along the soma-apical dendritic axis. We found that these dendrites are relatively compact with 50% maximal somatic current loss for synaptic inputs arriving at distal dendritic regions. Distal dendrites could generate small and fast local spikes, but they had little impact on the soma, indicating that they are only weakly active. In contrast to the neocortex, we found no evidence for dendritic Ca2+ or NMDA spikes though these dendrites actively supported action potential backpropagation with concomitant entry of Ca2+ ions. Based on experiments and simulations we suggest that regardless of dendritic location, olfactory bulb inputs have nearly uniform potency and are distributed diffusely over the distal apical tree (layer Ia), thereby minimizing sublinear summation effects. This indicates that any stimulus feature extraction performed by these cells will occur at the soma and is based on the nearly linear sum of olfactory bulb inputs, rather than on explicitly designed clusters of functionally related synapses in the dendritic tree.
引用
收藏
页码:12641 / 12652
页数:12
相关论文
共 48 条
[1]  
Arbib M.A., 1997, NEURAL ORG STRUCTURE
[2]   Dynamic ensemble odor coding in the mammalian olfactory bulb: Sensory information at different timescales [J].
Bathellier, Brice ;
Buhl, Derek L. ;
Accolla, Riccardo ;
Carleton, Alan .
NEURON, 2008, 57 (04) :586-598
[3]   Synaptic modifications in cultured hippocampal neurons: Dependence on spike timing, synaptic strength, and postsynaptic cell type [J].
Bi, GQ ;
Poo, MM .
JOURNAL OF NEUROSCIENCE, 1998, 18 (24) :10464-10472
[4]   Simple networks for spike-timing-based computation, with application to olfactory processing [J].
Brody, CD ;
Hopfield, JJ .
NEURON, 2003, 37 (05) :843-852
[5]   ELECTRO-PHYSIOLOGICAL CHARACTERIZATION OF REMOTE CHEMICAL SYNAPSES [J].
CARNEVALE, NT ;
JOHNSTON, D .
JOURNAL OF NEUROPHYSIOLOGY, 1982, 47 (04) :606-621
[6]   Strong single-fiber sensory inputs to olfactory cortex: Implications for olfactory coding [J].
Franks, KM ;
Isaacson, JS .
NEURON, 2006, 49 (03) :357-363
[7]   Spike-timing-dependent synaptic plasticity depends on dendritic location [J].
Froemke, RC ;
Poo, MM ;
Dan, Y .
NATURE, 2005, 434 (7030) :221-225
[8]   Mechanism of block by ZD 7288 of the hyperpolarization-activated inward rectifying current in guinea pig substantia nigra neurons in vitro [J].
Harris, NC ;
Constanti, A .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 74 (06) :2366-2378
[9]  
HASSELMO ME, 1990, COLD SH Q B, V55, P599
[10]   Differential shunting of EPSPs by action potentials [J].
Häusser, M ;
Major, G ;
Stuart, GJ .
SCIENCE, 2001, 291 (5501) :138-141