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 270: C1145-C1152, 1996;
0363-6143/96 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Estacion, M.
Right arrow Articles by Gargus, J. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Estacion, M.
Right arrow Articles by Gargus, J. J.

AJP - Cell Physiology, Vol 270, Issue 4 C1145-C1152, Copyright © 1996 by American Physiological Society


ARTICLES

Calcium is permeable through a maitotoxin-activated nonselective cation channel in mouse L cells

M. Estacion, H. B. Nguyen and J. J. Gargus
Department of Physiology and Biophysics, University of California, Irvine 92717, USA.

The shellfish poison maitotoxin causes the irreversible opening of nonselective cation channels in mouse L cell fibroblasts, consistent with the action of this toxin in other cell types and the previously demonstrated existence of 28-pS voltage-insensitive nonselected cation channels that are activated by platelet-derived growth factor in these cells. Toxin-induced opening of these nonselective cation channels led to increases of intracellular calcium and secondary activation of calcium-activated potassium channel. These effects were completely dependent on influx of extracellular calcium, supporting the conclusion that the maitotoxin-activated nonselective cation channels are permeable to calcium as well as to sodium and potassium. The implication of this finding is that calcium signaling through this channel underlies its links into the growth factor response.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Estacion, J. S. Weinberg, W. G. Sinkins, and W. P. Schilling
Blockade of maitotoxin-induced endothelial cell lysis by glycine and L-alanine
Am J Physiol Cell Physiol, April 1, 2003; 284(4): C1006 - C1020.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
W. P. Schilling, W. G. Sinkins, and M. Estacion
Maitotoxin activates a nonselective cation channel and a P2Z/P2X7-like cytolytic pore in human skin fibroblasts
Am J Physiol Cell Physiol, October 1, 1999; 277(4): C755 - C765.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. A. Leech and J. F. Habener
Insulinotropic Glucagon-like Peptide-1-mediated Activation of Non-selective Cation Currents in Insulinoma Cells Is Mimicked by Maitotoxin
J. Biol. Chem., July 18, 1997; 272(29): 17987 - 17993.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online