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Volume 17, Number 19,
Issue of October 1, 1997
pp. 7359-7371
Copyright ©1997 Society for Neuroscience
Impact of Cytoplasmic Calcium Buffering on the Spatial and
Temporal Characteristics of Intercellular Calcium Signals in
Astrocytes
Received Feb. 14, 1997; revised June 19, 1997; accepted July 11, 1997.
Zhong Wang1,
Michael Tymianski2,
Owen T. Jones2, and
Maiken Nedergaard1
1 Departments of Cell Biology and Anatomy and
Neurosurgery, New York Medical College, Valhalla, New York 10595, and
2 Playfair Neuroscience Unit, University of Toronto, The
Toronto Hospital-Western Division, Toronto, Ontario, Canada M5T-2S8
The impact of calcium buffering on the initiation and propagation
of mechanically elicited intercellular Ca2+ waves
was studied using astrocytes loaded with different exogenous, cell
membrane-permeant Ca2+ chelators and a laser
scanning confocal or video fluorescence microscope. Using an ELISA with
a novel antibody to BAPTA, we showed that different cell-permeant
chelators, when applied at the same concentrations, accumulate to the
same degree inside the cells. Loading cultures with BAPTA, a high
Ca2+ affinity chelator, almost completely blocked
calcium wave occurrence. Chelators having lower Ca2+
affinities had lesser affects, as shown in their attenuation of both
the radius of spread and propagation velocity of the
Ca2+ wave. The chelators blocked the process of wave
propagation, not initiation, because large
[Ca2+]i increases elicited in the
mechanically stimulated cell were insufficient to trigger the wave in
the presence of high Ca2+ affinity buffers. Wave
attenuation was a function of cytoplasmic Ca2+
buffering capacity; i.e., loading increasing concentrations of low
Ca2+ affinity buffers mimicked the effects of lesser
quantities of high-affinity chelators. In chelator-treated astrocytes,
changes in calcium wave properties were independent of the
Ca2+-binding rate constants of the chelators, of
chelation of other ions such as Zn2+, and of effects
on gap junction function. Slowing of the wave could be completely
accounted for by the slowing of Ca2+ ion diffusion
within the cytoplasm of individual astrocytes. The data obtained
suggest that alterations in Ca2+ buffering may
provide a potent mechanism by which the localized spread of astrocytic
Ca2+ signals is controlled.
Key words:
calcium buffering;
astrocytes;
calcium chelators;
BAPTA;
calcium waves;
cell culture;
digital imaging
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