WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, April 30, 2008, 28(18):4640-4648; doi:10.1523/JNEUROSCI.5486-07.2008

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
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 Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hurlock, E. C.
Right arrow Articles by Joho, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hurlock, E. C.
Right arrow Articles by Joho, R. H.

 Previous Article  |  Next Article 

Cellular/Molecular
Purkinje-Cell-Restricted Restoration of Kv3.3 Function Restores Complex Spikes and Rescues Motor Coordination in Kcnc3 Mutants

Edward C. Hurlock, Anne McMahon, and Rolf H. Joho

Department of Neuroscience, The University of Texas Southwestern Medical Center, Dallas, Texas 75390

Correspondence should be addressed to Dr. Rolf H. Joho, Department of Neuroscience, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9111. Email: rolf.joho{at}utsouthwestern.edu

The fast-activating/deactivating voltage-gated potassium channel Kv3.3 (Kcnc3) is expressed in various neuronal cell types involved in motor function, including cerebellar Purkinje cells. Spinocerebellar ataxia type 13 (SCA13) patients carrying dominant-negative mutations in Kcnc3 and Kcnc3-null mutant mice both display motor incoordination, suggested in mice by increased lateral deviation while ambulating and slips on a narrow beam. Motor skill learning, however, is spared. Mice lacking Kcnc3 also exhibit muscle twitches. In addition to broadened spikes, recordings of Kcnc3-null Purkinje cells revealed fewer spikelets in complex spikes and a lower intraburst frequency. Targeted reexpression of Kv3.3 channels exclusively in Purkinje cells in Kcnc3-null mice as well as in mice also heterozygous for Kv3.1 sufficed to restore simple spike brevity along with normal complex spikes and to rescue specifically coordination. Therefore, spike parameters requiring Kv3.3 function in Purkinje cells are involved in the ataxic null phenotype and motor coordination, but not motor learning.

Key words: K channels; burst firing; motor dysfunction; cerebellum; Purkinje cell; complex spike


Received Dec. 12, 2007; revised March 14, 2008; accepted March 17, 2008.

Correspondence should be addressed to Dr. Rolf H. Joho, Department of Neuroscience, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9111. Email: rolf.joho{at}utsouthwestern.edu




This article has been cited by other articles:


Home page
Arch NeurolHome page
V. G. Shakkottai and H. L. Paulson
Physiologic Alterations in Ataxia: Channeling Changes Into Novel Therapies
Arch Neurol, October 1, 2009; 66(10): 1196 - 1201.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. Ros, R. N. S. Sachdev, Y. Yu, N. Sestan, and D. A. McCormick
Neocortical Networks Entrain Neuronal Circuits in Cerebellar Cortex
J. Neurosci., August 19, 2009; 29(33): 10309 - 10320.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-