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J Neurophysiol 102: 735-751, 2009. First published May 20, 2009; doi:10.1152/jn.00083.2009
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Postnatal Development of Dendritic Synaptic Integration in Rat Neocortical Pyramidal Neurons

Susan E. Atkinson and Stephen R. Williams

Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom

Submitted 27 January 2009; accepted in final form 12 May 2009

The dendritic tree of layer 5 (L5) pyramidal neurons spans the neocortical layers, allowing the integration of intra- and extracortical synaptic inputs. Here we investigate the postnatal development of the integrative properties of rat L5 pyramidal neurons using simultaneous whole cell recording from the soma and distal apical dendrite. In young (P9-10) neurons, apical dendritic excitatory synaptic input powerfully drove action potential output by efficiently summating at the axonal site of action potential generation. In contrast, in mature (P25-29) neurons, apical dendritic excitatory input provided little direct depolarization at the site of action potential generation but was integrated locally in the apical dendritic tree leading to the generation of dendritic spikes. Consequently, over the first postnatal month the fraction of action potentials driven by apical dendritic spikes increased dramatically. This developmental remodeling of the integrative operations of L5 pyramidal neurons was controlled by a >10-fold increase in the density of apical dendritic Hyperpolarization-activated cyclic nucleotide (HCN)-gated channels found in cell-attached patches or by immunostaining for the HCN channel isoform HCN1. Thus an age-dependent increase in apical dendritic HCN channel density ensures that L5 pyramidal neurons develop from compact temporal integrators to compartmentalized integrators of basal and apical dendritic synaptic input.


Address for reprint requests and other correspondence: S. R. Williams, Neurobiology Div., MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK (E-mail: srw{at}mrc-lmb.cam.ac.uk)







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