Am J Physiol Cell Physiol Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 291: C138-C146, 2006. First published February 22, 2006; doi:10.1152/ajpcell.00629.2005
0363-6143/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
291/1/C138    most recent
00629.2005v1
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 ISI Web of Science (15)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kang, D.
Right arrow Articles by Kim, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kang, D.
Right arrow Articles by Kim, D.

MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

TREK-2 (K2P10.1) and TRESK (K2P18.1) are major background K+ channels in dorsal root ganglion neurons

Dawon Kang1,2 and Donghee Kim1

1Department of Physiology and Biophysics, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois; and 2Department of Physiology, College of Medicine and Institute of Health Science, Gyeongsang National University, Jinju, Korea

Submitted 15 December 2005 ; accepted in final form 15 February 2006

Dorsal root ganglion (DRG) neurons express mRNAs for many two-pore domain K+ (K2P) channels that behave as background K+ channels. To identify functional background K+ channels in DRG neurons, we examined the properties of single-channel openings from cell-attached and inside-out patches from the cell bodies of DRG neurons. We found seven types of K+ channels, with single-channel conductance ranging from 14 to 120 pS in 150 mM KCl bath solution. Four of these K+ channels showed biophysical and pharmacological properties similar to TRESK (14 pS), TREK-1 (112 pS), TREK-2 (50 pS), and TRAAK (73 pS), which are members of the K2P channel family. The molecular identity of the three other K+ channels could not be determined, as they showed low channel activity and were observed infrequently. Of the four K2P channels, the TRESK-like (14 pS) K+ channel was most active at 24°C. At 37°C, the 50-pS (TREK-2 like) channel was the most active and contributed the most (69%) to the resting K+ current, followed by the TRESK-like 14-pS (16%), TREK-1-like 112-pS (12%), and TRAAK-like 73-pS (3%) channels. In DRG neurons, mRNAs of all four K2P channels, as well as those of TASK-1 and TASK-3, were expressed, as judged by RT-PCR analysis. Our results show that TREKs and TRESK together contribute >95% of the background K+ conductance of DRG neurons at 37°C. As TREKs and TRESK are targets of modulation by receptor agonists, they are likely to play an active role in the regulation of excitability in DRG neurons.

two-pore domain K+ channel; conductance; excitability



Address for reprint requests and other correspondence: D. Kim, Dept. of Physiology and Biophysics, Rosalind Franklin Univ. of Medicine and Science, Chicago Medical School, 3333 Green Bay Road, North Chicago, IL 60064 (e-mail: donghee.kim{at}rosalindfranklin.edu)




This article has been cited by other articles:


Home page
J. Physiol.Home page
D. Simkin, E. J. Cavanaugh, and D. Kim
Control of the single channel conductance of K2P10.1 (TREK-2) by the amino-terminus: role of alternative translation initiation
J. Physiol., December 1, 2008; 586(23): 5651 - 5663.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. Dobler, A. Springauf, S. Tovornik, M. Weber, A. Schmitt, R. Sedlmeier, E. Wischmeyer, and F. Doring
TRESK two-pore-domain K+ channels constitute a significant component of background potassium currents in murine dorsal root ganglion neurones
J. Physiol., December 15, 2007; 585(3): 867 - 879.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. Kang, C. Choe, E. Cavanaugh, and D. Kim
Properties of single two-pore domain TREK-2 channels expressed in mammalian cells
J. Physiol., August 15, 2007; 583(1): 57 - 69.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
T. Yang, E. Esteve, I. N. Pessah, T. F. Molinski, P. D. Allen, and J. R. Lopez
Elevated resting [Ca2+]i in myotubes expressing malignant hyperthermia RyR1 cDNAs is partially restored by modulation of passive calcium leak from the SR
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1591 - C1598.
[Abstract] [Full Text] [PDF]


Home page
GutHome page
J. R O'Hara, A. E Lomax, G. M Mawe, and K. A Sharkey
Ileitis alters neuronal and enteroendocrine signalling in guinea pig distal colon
Gut, February 1, 2007; 56(2): 186 - 194.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. Mathie
Neuronal two-pore-domain potassium channels and their regulation by G protein-coupled receptors
J. Physiol., January 15, 2007; 578(2): 377 - 385.
[Abstract] [Full Text] [PDF]




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