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J Neurophysiol 102: 1218-1226, 2009. First published June 24, 2009; doi:10.1152/jn.90513.2008
0022-3077/09 $8.00
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Dendritic Calcium Channels and Their Activation by Synaptic Signals in Auditory Coincidence Detector Neurons

Trillium Blackmer, Sidney P. Kuo*, Kevin J. Bender*, Pierre F. Apostolides* and Laurence O. Trussell

Vollum Institute and Oregon Hearing Research Center, Oregon Health and Science University, Portland, Oregon

Submitted 28 April 2008; accepted in final form 11 June 2009

The avian nucleus laminaris (NL) encodes the azimuthal location of low-frequency sound sources by detecting the coincidence of binaural signals. Accurate coincidence detection requires precise developmental regulation of the lengths of the fine, bitufted dendrites that characterize neurons in NL. Such regulation has been suggested to be driven by local, synaptically mediated, dendritic signals such as Ca2+. We examined Ca2+ signaling through patch clamp and ion imaging experiments in slices containing nucleus laminaris from embryonic chicks. Voltage-clamp recordings of neurons located in the NL showed the presence of large Ca2+ currents of two types, a low voltage–activated, fast inactivating Ni2+ sensitive channel resembling mammalian T-type channels, and a high voltage–activated, slowly inactivating Cd2+ sensitive channel. Two-photon Ca2+ imaging showed that both channel types were concentrated on dendrites, even at their distal tips. Single action potentials triggered synaptically or by somatic current injection immediately elevated Ca2+ throughout the entire cell. Ca2+ signals triggered by subthreshold synaptic activity were highly localized. Thus when electrical activity is suprathreshold, Ca2+ channels ensure that Ca2+ rises in all dendrites, even those that are synaptically inactive.


Address for reprint requests and other correspondence: L. O. Trussell, Oregon Health and Science Univ., 3181 SW Sam Jackson Park Rd., L335A, Portland, OR 97239 (E-mail: trussell{at}ohsu.edu)







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