The Journal of General Physiology
Cell MicroControls
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Published 1 July 2001. doi:10.1085/jgp.118.1.11
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© The Rockefeller University Press, 0022-1295/2001//11/ $5.00
Journal of General Physiology, Volume 118, Number 1, 2001


Original Article

Electrically Triggered All-or-None Ca2+-Liberation during Action Potential in the Giant Alga Chara

Michael Wacke and Gerhard Thiela

a Albrecht-von-Haller Institute for Plant Sciences, Plant Biophysics, University of Göttingen, 37073 Göttingen, Germany
Department of Botany, TU-Darmstadt, Schnittspahnstrasse 3, 64287 Darmstadt, Germany.49-6151-164630

thiel{at}bio.tu-darmstadt.de

Electrically triggered action potentials in the giant alga Chara corallina are associated with a transient rise in the concentration of free Ca2+ in the cytoplasm (Ca2+cyt). The present measurements of Ca2+cyt during membrane excitation show that stimulating pulses of low magnitude (subthreshold pulse) had no perceivable effect on Ca2+cyt. When the strength of a pulse exceeded a narrow threshold (suprathreshold pulse) it evoked the full extent of the Ca2+cyt elevation. This suggests an all-or-none mechanism for Ca2+ mobilization. A transient calcium rise could also be induced by one subthreshold pulse if it was after another subthreshold pulse of the same kind after a suitable interval, i.e., not closer than a few 100 ms and not longer than a few seconds. This dependency of Ca2+ mobilization on single and double pulses can be simulated by a model in which a second messenger is produced in a voltage-dependent manner. This second messenger liberates Ca2+ from internal stores in an all-or-none manner once a critical concentration (threshold) of the second messenger is exceeded in the cytoplasm. The positive effect of a single suprathreshold pulse and two optimally spaced subthreshold pulses on Ca2+ mobilization can be explained on the basis of relative velocity for second messenger production and decomposition as well as the availability of the precursor for the second messenger production. Assuming that inositol-1,4,5,-trisphosphate (IP3) is the second messenger in question, the present data provide the major rate constants for IP3 metabolism.

Key Words: calcium mobilization • Fura-2 • simulation • voltage-dependent second messenger production


© 2001 The Rockefeller University Press


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