|
|
||||||||
The Journal of Neurophysiology Vol. 84 No. 6 December 2000, pp. 2888-2895
Copyright ©2000 by the American Physiological Society
1Curriculum in Oral Biology, School of Dentistry and 2Department of Cell and Molecular Physiology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599
Wang, Haibin and
Gerry
S. Oxford.
Voltage-Dependent Ion Channels in CAD Cells: A
Catecholaminergic Neuronal Line That Exhibits Inducible Differentiation. J. Neurophysiol. 84: 2888-2895, 2000. Cell
lines derived from tumors engineered in the CNS offer promise as models
of specific neuronal cell types. CAD cells are an unusual
subclone of a murine cell line derived from tyrosine hydroxylase (TH)
driven tumorigenesis, which undergoes reversible morphological
differentiation on serum deprivation. Using single-cell electrophysiology we have examined the properties of ion channels expressed in CAD cells. Despite relatively low resting potentials, CAD
cells can be induced to fire robust action potentials when mildly
artificially hyperpolarized. Correspondingly, voltage-dependent sodium
and potassium currents were elicited under voltage clamp. Sodium
currents are TTX sensitive and exhibit conventional activation and
inactivation properties. The potassium currents reflected two
pharmacologically distinguishable populations of delayed rectifier type
channels while no transient A-type channels were observed. Using barium
as a charge carrier, we observed an inactivating current that was
completely blocked by nimodipine and thus associated with L-type
calcium channels. On differentiation, three changes in functional
channel expression occurred; a 4-fold decrease in sodium current
density, a 1.5-fold increase in potassium current density, and the
induction of a small noninactivating barium current component. The
neuronal morphology, excitability properties, and changes in channel
function with differentiation make CAD cells an attractive model for
study of catecholaminergic neurons.
This article has been cited by other articles:
![]() |
M. J. McFarland, T. K. Bardell, M. L. Yates, E. A. Placzek, and E. L. Barker RNA Interference-Mediated Knockdown of Dynamin 2 Reduces Endocannabinoid Uptake into Neuronal dCAD Cells Mol. Pharmacol., July 1, 2008; 74(1): 101 - 108. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. Sousa, J. S. Berg, B. W. Robertson, R. B. Meeker, and R. E. Cheney Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons J. Cell Sci., January 1, 2006; 119(1): 184 - 194. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Colton, Q. Xu, J. R. Burke, S. Y. Bae, J. K. Wakefield, A. Nair, W. J. Strittmatter, and M. P. Vitek Disrupted Spermine Homeostasis: A Novel Mechanism in Polyglutamine-Mediated Aggregation and Cell Death J. Neurosci., August 11, 2004; 24(32): 7118 - 7127. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |