Dendrite-to-Soma Input/Output Function of Continuous Time-Varying Signals in Hippocampal CA1 Pyramidal Neurons
Author(s) -
Erik P. Cook,
Jennifer A. Guest,
Yong Liang,
Nicolas Y. Masse,
Costa M. Colbert
Publication year - 2007
Publication title -
journal of neurophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.302
H-Index - 245
eISSN - 1522-1598
pISSN - 0022-3077
DOI - 10.1152/jn.00414.2007
Subject(s) - soma , apical dendrite , pyramidal cell , subthreshold conduction , stimulus (psychology) , dendritic spike , dendrite (mathematics) , neuroscience , hippocampal formation , control theory (sociology) , automatic gain control , biological system , excitatory postsynaptic potential , physics , mathematics , biology , computer science , inhibitory postsynaptic potential , psychology , voltage , cmos , transistor , artificial intelligence , psychotherapist , amplifier , geometry , control (management) , quantum mechanics , optoelectronics
We examined how hippocamal CA1 neurons process complex time-varying inputs that dendrites are likely to receive in vivo. We propose a functional model of the dendrite-to-soma input/output relationship that combines temporal integration and static-gain control mechanisms. Using simultaneous dual whole cell recordings, we injected 50 s of subthreshold and suprathreshold zero-mean white-noise current into the primary dendritic trunk along the proximal 2/3 of stratum radiatum and measured the membrane potential at the soma. Applying a nonlinear system-identification analysis, we found that a cascade of a linear filter followed by an adapting static-gain term fully accounted for the nonspiking input/output relationship between the dendrite and soma. The estimated filters contained a prominent band-pass region in the 1- to 10-Hz frequency range that remained constant as a function of stimulus variance. The gain of the dendrite-to-soma input/output relationship, in contrast, varied as a function of stimulus variance. When the contribution of the voltage-dependent current I(h) was eliminated, the estimated filters lost their band-pass properties and the gain regulation was substantially altered. Our findings suggest that the dendrite-to-soma input/output relationship for proximal apical inputs to CA1 pyramidal neurons is well described as a band-pass filter in the theta frequency range followed by a gain-control nonlinearity that dynamically adapts to the statistics of the input signal.
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