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(Received for publication, March 11, 1997, and in revised form, April 30, 1997)
From the Department of Physiology, Emory University School of
Medicine, Atlanta, Georgia 30322
Cyclic ADP-ribose (cADPr) has been shown to
release intracellular Ca2+ from sea urchin eggs and a
variety of vertebrate cell types, although its mechanism of action
remains elusive. We employed the caged version of cADPr to study the
[Ca2+] transient kinetics in intact sea urchin eggs for
insights into how cADPr gates Ca2+ release.
Ca2+ release triggered by photolytic production of cADPr
was initially slow, with an effective delay of several hundred
milliseconds before the onset of a rapid Ca2+ release
phase. In contrast, Ca2+ release induced by photolysis of
caged inositol 1,4,5-trisphosphate was immediate in onset and roughly
an order of magnitude faster. The delay before cADPr-induced
Ca2+ release was eliminated when the [Ca2+]
was step-elevated coincident with the photoliberation of cADPr and
greatly prolonged in the presence of exogenous Ca2+
buffers. Thus, the slow onset of Ca2+ release does not
reflect an intrinsically slow rate by which cADPr gates release
channels. Rather, a [Ca2+] rise from resting levels is
needed to achieve more than minimal cADPr activity. Full release of
Ca2+ by cADPr in intact sea urchin eggs requires a positive
Ca2+ feedback.
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