Transitional Changes in Membrane Potential and Intracellular [Ca2+] in Rat Basophilic Leukemia Cells

Transitional Changes in Membrane Potential and Intracellular [Ca2+] in Rat Basophilic Leukemia Cells Using whole-cell current-clamp measurements we have found that thapsigargin-mediated activation of store-regulated Ca2+ entry in rat basophilic leukemia cells is accompanied by complex changes in membrane potential. These changes consisted of: (i) an initial slow, small depolarization, (ii) a transitional change in potential to a depolarized value and (iii) transitional changes between a hyperpolarized and a depolarized potential. These complex changes in potential can be explained by the interaction between the endogenous inwardly rectifying K+ conductance and the generation of a small inward current. To investigate the possible influence of these changes of potential on [Ca2+] i , single cell measurements of fura2 fluorescence were undertaken alone or in combination with current-clamp measurements. Thapsigargin-mediated activation of the store-regulated Ca2+ entry pathway was accompanied by a marked increase of [Ca2+] i . During this increase, transient, abrupt declines in [Ca2+] i were detected in approximately 60% of the cells investigated. These changes of [Ca2+] i are consistent with the observed changes of membrane potential recorded under current-clamp. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The Journal of Membrane Biology Springer Journals

Transitional Changes in Membrane Potential and Intracellular [Ca2+] in Rat Basophilic Leukemia Cells

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Publisher
Springer-Verlag
Copyright
Copyright © Inc. by 1999 Springer-Verlag New York
Subject
Life Sciences; Biochemistry, general; Human Physiology
ISSN
0022-2631
eISSN
1432-1424
D.O.I.
10.1007/s002329900539
Publisher site
See Article on Publisher Site

Abstract

Using whole-cell current-clamp measurements we have found that thapsigargin-mediated activation of store-regulated Ca2+ entry in rat basophilic leukemia cells is accompanied by complex changes in membrane potential. These changes consisted of: (i) an initial slow, small depolarization, (ii) a transitional change in potential to a depolarized value and (iii) transitional changes between a hyperpolarized and a depolarized potential. These complex changes in potential can be explained by the interaction between the endogenous inwardly rectifying K+ conductance and the generation of a small inward current. To investigate the possible influence of these changes of potential on [Ca2+] i , single cell measurements of fura2 fluorescence were undertaken alone or in combination with current-clamp measurements. Thapsigargin-mediated activation of the store-regulated Ca2+ entry pathway was accompanied by a marked increase of [Ca2+] i . During this increase, transient, abrupt declines in [Ca2+] i were detected in approximately 60% of the cells investigated. These changes of [Ca2+] i are consistent with the observed changes of membrane potential recorded under current-clamp.

Journal

The Journal of Membrane BiologySpringer Journals

Published: Jul 1, 1999

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