JN Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 96: 3194-3208, 2006. First published September 13, 2006; doi:10.1152/jn.00484.2006
0022-3077/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
96/6/3194    most recent
00484.2006v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Verbny, Y. I.
Right arrow Articles by Banks, M. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Verbny, Y. I.
Right arrow Articles by Banks, M. I.

Properties of a Population of GABAergic Cells in Murine Auditory Cortex Weakly Excited by Thalamic Stimulation

Yakov I. Verbny1, Ferenc Erdélyi2, Gábor Szabó2 and Matthew I. Banks1

1Department of Anesthesiology, University of Wisconsin, Madison, Wisconsin; and 2Department of Gene Technology and Developmental Neurobiology, Institute of Experimental Medicine, Budapest, Hungary

Submitted 7 May 2006; accepted in final form 7 September 2006

Feedforward inhibition triggered by thalamocortical (TC) afferents sharpens onset responses and shapes receptive fields of pyramidal cells in auditory cortex (ACx). Previous studies focused only on interneurons located in and around layer IV in primary ACx, target of the dense thalamic projections from ventral medial geniculate. We investigated a population of feedforward interneurons located throughout layers I–V and activated by both afferents from primary and nonprimary thalamus using recordings from auditory TC brain slices obtained from mice expressing green fluorescent protein under control of the glutamic acid decarboxylase (GAD65) promoter in a subpopulation of cortical GABAergic cells. We studied the responses of these interneurons and of pyramidal cells in ACx to thalamic stimulation and to hyper- and depolarizing current pulses. Most interneurons exhibited monosynaptic responses to thalamic stimulation, but this excitation was weak and subthreshold. Interneurons had multipolar dendritic morphology with widespread and dense axonal projections extending several hundred micrometers from the soma. In pyramidal cells from layers II–IV, thalamic excitatory postsynaptic potentials were significantly larger than in interneurons and were superthreshold in 40% of cells, but in these cells, there was no evidence of feedforward inhibition. By contrast, feedforward inhibition was observed in 12 of 18 layer V pyramidal cells. Thus feedforward inhibition in supragranular layers of ACx is weak, and these interneurons require coincident excitation to be activated by thalamic inputs.


Address for reprint requests and other correspondence: Matthew I. Banks, Dept of Anesthesiology, University of Wisconsin, 1300 University Ave., Room 4605, Madison, WI 53706 (E-mail: mibanks{at}wisc.edu)




This article has been cited by other articles:


Home page
J. Neurosci.Home page
R. J. Richardson, J. A. Blundon, I. T. Bayazitov, and S. S. Zakharenko
Connectivity Patterns Revealed by Mapping of Active Inputs on Dendrites of Thalamorecipient Neurons in the Auditory Cortex
J. Neurosci., May 20, 2009; 29(20): 6406 - 6417.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
C. Ling, Y. I. Verbny, M. I. Banks, M. Sandor, and Z. Fabry
In Situ Activation of Antigen-Specific CD8+ T Cells in the Presence of Antigen in Organotypic Brain Slices
J. Immunol., June 15, 2008; 180(12): 8393 - 8399.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the The American Physiological Society.