The Journal of General Physiology
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Published online 15 March 2004 doi:10.1085/jgp.200308999
The Rockefeller University Press, 0022-1295 $8.00
JGP, Volume 123, Number 4, 377-386
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RYR2 Proteins Contribute to the Formation of Ca2+ Sparks in Smooth Muscle

Guangju Ji1, Morris E. Feldman1, Kai Su Greene1, Vincenzo Sorrentino2, Hong-Bo Xin1, and Michael I. Kotlikoff1

1 Department of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853
2 Molecular Medicine Section Department of Neuroscience, University of Siena, Siena, Italy 53100

Address correspondence to Michael Kotlikoff, Department of Biomedical Sciences, Cornell University, T4018 VRT, Box 11, Ithaca, NY 14853-6401. Fax: (607) 253-3317; email: mik7{at}cornell.edu

Calcium release through ryanodine receptors (RYR) activates calcium-dependent membrane conductances and plays an important role in excitation-contraction coupling in smooth muscle. The specific RYR isoforms associated with this release in smooth muscle, and the role of RYR-associated proteins such as FK506 binding proteins (FKBPs), has not been clearly established, however. FKBP12.6 proteins interact with RYR2 Ca2+ release channels and the absence of these proteins predictably alters the amplitude and kinetics of RYR2 unitary Ca2+ release events (Ca2+ sparks). To evaluate the role of specific RYR2 and FBKP12.6 proteins in Ca2+ release processes in smooth muscle, we compared spontaneous transient outward currents (STOCs), Ca2+ sparks, Ca2+-induced Ca2+ release, and Ca2+ waves in smooth muscle cells freshly isolated from wild-type, FKBP12.6-/-, and RYR3-/- mouse bladders. Consistent with a role of FKBP12.6 and RYR2 proteins in spontaneous Ca2+ sparks, we show that the frequency, amplitude, and kinetics of spontaneous, transient outward currents (STOCs) and spontaneous Ca2+ sparks are altered in FKBP12.6 deficient myocytes relative to wild-type and RYR3 null cells, which were not significantly different from each other. Ca2+ -induced Ca2+ release was similarly augmented in FKBP12.6-/-, but not in RYR3 null cells relative to wild-type. Finally, Ca2+ wave speed evoked by CICR was not different in RYR3 cells relative to control, indicating that these proteins are not necessary for normal Ca2+ wave propagation. The effect of FKBP12.6 deletion on the frequency, amplitude, and kinetics of spontaneous and evoked Ca2+ sparks in smooth muscle, and the finding of normal Ca2+ sparks and CICR in RYR3 null mice, indicate that Ca2+ release through RYR2 molecules contributes to the formation of spontaneous and evoked Ca2+ sparks, and associated STOCs, in smooth muscle.

Key Words: Ca2+ -induced Ca2+ release • ryanodine receptor • FKBP12.6 • RYR3 • knockout mouse


Abbreviations used in this paper: CICR, calcium-induced calcium release; SICR, stretch-induced calcium release; STOC, spontaneous, transient outward current.


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