help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
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 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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Koopman, W. J. H.
Right arrow Articles by Jenks, B. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koopman, W. J. H.
Right arrow Articles by Jenks, B. G.

Biophys J, July 2001, p. 57-65, Vol. 81, No. 1

Membrane-Initiated Ca2+ Signals Are Reshaped during Propagation to Subcellular Regions

Werner J. H. Koopman,* Wim J. J. M. Scheenen,* Rachel J. Errington,dagger Dagger Peter H. G. M. Willems,dagger René J. M. Bindels,Dagger Eric W. Roubos,* and Bruce G. Jenks*

Departments of  *Cellular Animal Physiology,  dagger Biochemistry, and  Dagger Cell Physiology, University of Nijmegen, Nijmegen, The Netherlands

An important aspect of Ca2+ signaling is the ability of cells to generate intracellular Ca2+ waves. In this study we have analyzed the cellular and subcellular kinetics of Ca2+ waves in a neuroendocrine transducer cell, the melanotrope of Xenopus laevis, using the ratiometric Ca2+ probe indo-1 and video-rate UV confocal laser-scanning microscopy. The purpose of the present study was to investigate how local Ca2+ changes contribute to a global Ca2+ signal; subsequently we quantified how a Ca2+ wave is kinetically reshaped as it is propagated through the cell. The combined kinetics of all subcellular Ca2+ signals determined the shape of the total cellular Ca2+ signal, but each subcellular contribution to the cellular signal was not constant in time. Near the plasma membrane, [Ca2+]i increased and decreased rapidly, processes that can be described by a linear and exponential function, respectively. In more central parts of the cell slower kinetics were observed that were best described by a Hill equation. This reshaping of the Ca2+ wave was modeled with an equation derived from a low-pass RC filter. We propose that the differences in spatial kinetics of the Ca2+ signal serves as a mechanism by which the same cellular Ca2+ signal carries different regulatory information to different subcellular regions of the cell, thus evoking differential cellular responses.

Biophys J, July 2001, p. 57-65, Vol. 81, No. 1
© 2001 by the Biophysical Society   0006-3495/01/07/57/09  $2.00



This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
W. J. H. Koopman, H.-J. Visch, S. Verkaart, L. W. P. J. van den Heuvel, J. A. M. Smeitink, and P. H. G. M. Willems
Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency
Am J Physiol Cell Physiol, October 1, 2005; 289(4): C881 - C890.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
W. J. H. Koopman, S. Verkaart, H.-J. Visch, F. H. van der Westhuizen, M. P. Murphy, L. W. P. J. van den Heuvel, J. A. M. Smeitink, and P. H. G. M. Willems
Inhibition of complex I of the electron transport chain causes O2-{middle dot}-mediated mitochondrial outgrowth
Am J Physiol Cell Physiol, June 1, 2005; 288(6): C1440 - C1450.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
Z. Cseresnyes and M. F. Schneider
Peripheral Hot Spots for Local Ca2+ Release after Single Action Potentials in Sympathetic Ganglion Neurons
Biophys. J., January 1, 2004; 86(1): 163 - 181.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
W. J. H. Koopman, M. Renders, A. Oosterhof, T. H. van Kuppevelt, B. G. M. van Engelen, and P. H. G. M. Willems
Upregulation of Ca2+ removal in human skeletal muscle: a possible role for Ca2+-dependent priming of mitochondrial ATP synthesis
Am J Physiol Cell Physiol, November 1, 2003; 285(5): C1263 - C1269.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
W. J. H. Koopman, R. R. Bosch, S. E. van Emst-de Vries, M. Spaargaren, J. J. H. H. M. De Pont, and P. H. G. M. Willems
R-Ras Alters Ca2+ Homeostasis by Increasing the Ca2+ Leak across the Endoplasmic Reticular Membrane
J. Biol. Chem., April 11, 2003; 278(16): 13672 - 13679.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
L. J. Janssen
Ionic mechanisms and Ca2+ regulation in airway smooth muscle contraction: do the data contradict dogma?
Am J Physiol Lung Cell Mol Physiol, June 1, 2002; 282(6): L1161 - L1178.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. J. C. de Groof, J. A. M. Fransen, R. J. Errington, P. H. G. M. Willems, B. Wieringa, and W. J. H. Koopman
The Creatine Kinase System Is Essential for Optimal Refill of the Sarcoplasmic Reticulum Ca2+ Store in Skeletal Muscle
J. Biol. Chem., February 8, 2002; 277(7): 5275 - 5284.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the Biophysical Society.