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Volume 272, Number 45,
Issue of November 7, 1997
pp. 28274-28280
©1997 by The American Society for Biochemistry and Molecular Biology, Inc.
Measurement of Ca2+ Fluxes during Elicitation of the
Oxidative Burst in Aequorin-transformed Tobacco Cells
(Received for publication, April 4, 1997, and in revised form, August 4, 1997)
Sreeganga
Chandra
and
Philip S.
Low
From the Department of Chemistry, Purdue University, West
Lafayette, Indiana 47907
We have employed suspension cultured
aequorin-transformed tobacco cells to examine the involvement of
Ca2+ in signal transduction of the oxidative burst.
Use of cultured cells for this purpose was validated by demonstrating
that the cells responded to cold shock quantitatively and qualitatively similarly to the intact transgenic plants from which they were derived.
Stimulation of the oxidative burst in the cell suspension was achieved
by administration of oligogalacturonic acid, Mas-7 (a peptide known to
activate G proteins and Ca2+ fluxes), hypo-osmotic stress,
or harpin (a protein from the pathogenic bacterium Erwinia
amylovora). The latter failed to promote any detectable increase
in cytoplasmic Ca2+ concentration, whereas each of the
former three triggered a rapid rise in cytosolic Ca2+
followed by a return within seconds to basal Ca2+ levels.
Peak Ca2+ concentrations induced by the former three
elicitors were ~0.7, 1.4, and 1.3 µM, respectively.
Three lines of evidence suggest that the observed Ca2+
pulses are essential to transduction of the oxidative burst signals by
their respective elicitors: (i) inhibition of the Ca2+
transients with Ca2+ chelators or Ca2+ channel
blockers prevented expression of the oxidative burst, (ii) introduction
of exogenous Ca2+ into the same cells initiated the burst
even in the absence of other inducers of the response, and (iii) the
observed Ca2+ transients often returned to near basal
levels well before any H2O2 synthesis could be
detected, suggesting that the Ca2+ influx is required to
communicate the burst signal but not maintain the defense response.
These data suggest that Ca2+ pulses serve frequently, but
not invariably, to transduce an oxidative burst signal.

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Copyright © 1997 by the American Society for Biochemistry and Molecular Biology.
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