|
|
||||||||
Journal of Neurophysiology, Vol 73, Issue 6 2522-2534, Copyright © 1995 by APS
ARTICLES |
P. A. Goldstein, C. J. Lee and A. B. MacDermott
Department of Physiology and Cellular Biophysics, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA.
1. By measuring the apparent reversal potential (aErev) of kainate- and alpha-amino-3-hydroxyl-5-methyl-4-isoxazole propionic acid (AMPA)-evoked currents associated with changes in extracellular Ca2+ concentration ([Ca2+]e), we have been able to identify embryonic dorsal horn neurons grown in tissue culture that express Ca(2+)-permeable non-N-methyl-D-aspartic acid (NMDA) receptors. 2. The relative expression of Ca(2+)-permeable and Ca(2+)-impermeable non-NMDA receptors varies from cell to cell. This was evident from the range of a ErevS observed for kainate-evoked currents in a 0 mM [Na+]e, 10 mM [Ca2+]e bath. Under these conditions, aErev ranged from -96 to -21 mV, suggesting that the percentage of the non-NMDA receptors on each neuron that are Ca(2+)-permeable is variable. 3. To determine the extent to which the variability in aErev is due to variable receptor expression rather than experimental variability, we compared the effects of changes in [Ca2+]e on kainate-evoked currents and NMDA-evoked currents on the same cells. Assuming that all of the NMDA receptors on each neuron have a similar Ca2+ permeability, this approach provides an index of the sensitivity of our assay system. The reversal potential of NMDA-evoked currents in 10 mM [Ca2+]e ranged from -30 to -7 mV, whereas on the same population of neurons, the aErev of kainate-evoked currents ranged from -92 to -40 mV. 4. The rectification properties of the non-NMDA currents were generally linear or outwardly rectifying in normal bath solution. When the PCa/PCs ratio in 0 mM [Na+]e, 10 mM [Ca2+]e bath solution was assessed as a function of the rectification index in standard bath, a poor correlation was found between Ca2+ permeability and the rectification index. 5. The aErev of kainate-evoked currents was similar to that of cyclothiazide-enhanced AMPA-evoked currents observed on the same cells (-66.5 +/- 18.4 and -64.0 +/- 13.9 mV, mean +/- SD, respectively). This suggests that kainate is primarily activating the AMPA receptor and that the majority of non-NMDA receptors on embryonic dorsal horn neurons in culture are high-affinity AMPA receptors. 6. Immunocytochemical evidence suggests that the AMPA receptor subunits GluR1-4 are expressed to a variable degree from cell to cell in our cultures. We found evidence for low levels of expression of the kainate receptor subunits GluR5-7. The immunocytochemical observations support the physiological data indicating that much of the kainate-evoked current recorded in our experiments can be accounted for by kainate activation of AMPA receptors.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
M. Antal, Y. Fukazawa, M. Eordogh, D. Muszil, E. Molnar, M. Itakura, M. Takahashi, and R. Shigemoto Numbers, Densities, and Colocalization of AMPA- and NMDA-Type Glutamate Receptors at Individual Synapses in the Superficial Spinal Dorsal Horn of Rats J. Neurosci., September 24, 2008; 28(39): 9692 - 9701. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tsuzuki, H. Xing, J. Ling, and J. G. Gu Menthol-Induced Ca2+ Release from Presynaptic Ca2+ Stores Potentiates Sensory Synaptic Transmission J. Neurosci., January 21, 2004; 24(3): 762 - 771. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Ogoshi and J. H. Weiss Heterogeneity of Ca2+-Permeable AMPA/Kainate Channel Expression in Hippocampal Pyramidal Neurons: Fluorescence Imaging and Immunocytochemical Assessment J. Neurosci., November 19, 2003; 23(33): 10521 - 10530. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Van Damme, L. Van den Bosch, E. Van Houtte, G. Callewaert, and W. Robberecht GluR2-Dependent Properties of AMPA Receptors Determine the Selective Vulnerability of Motor Neurons to Excitotoxicity J Neurophysiol, September 1, 2002; 88(3): 1279 - 1287. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Vandenberghe, W. Robberecht, and J. R. Brorson AMPA Receptor Calcium Permeability, GluR2 Expression, and Selective Motoneuron Vulnerability J. Neurosci., January 1, 2000; 20(1): 123 - 132. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. R. Brorson, Z. Zhang, and W. Vandenberghe Ca2+ Permeation of AMPA Receptors in Cerebellar Neurons Expressing Glu Receptor 2 J. Neurosci., November 1, 1999; 19(21): 9149 - 9159. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. S. Engelman, T. B. Allen, and A. B. MacDermott The Distribution of Neurons Expressing Calcium-Permeable AMPA Receptors in the Superficial Laminae of the Spinal Cord Dorsal Horn J. Neurosci., March 15, 1999; 19(6): 2081 - 2089. [Abstract] [Full Text] [PDF] |
||||
![]() |
T.-L. Xu, J.-S. Li, Y.-H. Jin, and N. Akaike Modulation of the glycine response by Ca2+-permeable AMPA receptors in rat spinal neurones J. Physiol., February 1, 1999; 514(3): 701 - 711. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Washburn, M. Numberger, S. Zhang, and R. Dingledine Differential Dependence on GluR2 Expression of Three Characteristic Features of AMPA Receptors J. Neurosci., December 15, 1997; 17(24): 9393 - 9406. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. G. Carriedo, H. Z. Yin, and J. H. Weiss Motor Neurons Are Selectively Vulnerable to AMPA/Kainate Receptor-Mediated Injury In Vitro J. Neurosci., July 1, 1996; 16(13): 4069 - 4079. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |