Circulation Research. 2002
Published online before print July 8, 2002, doi: 10.1161/01.RES.0000028455.36940.5E
Published online before print July 8, 2002, doi: 10.1161/01.RES.0000028455.36940.5E
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Submitted on February 7, 2002
Revised on June 21, 2002
Accepted on June 24, 2002
Enhanced Basal Activity of a Cardiac Ca2+ Release Channel (Ryanodine Receptor) Mutant Associated With Ventricular Tachycardia and Sudden Death
Dawei Jiang ;
From the Cardiovascular Research Group, Departments of Physiology and Biophysics and Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta, Canada.
* To whom correspondence should be addressed. E-mail: swchen{at}ucalgary.ca.
Mutations in the human cardiac Ca2+ release channel (ryanodine receptor, RyR2) gene have recently been shown to cause effort-induced ventricular arrhythmias. However, the consequences of these disease-causing mutations in RyR2 channel function are unknown. In the present study, we characterized the properties of mutation R4496C of mouse RyR2, which is equivalent to a disease-causing human RyR2 mutation R4497C, by heterologous expression of the mutant in HEK293 cells. [3H]ryanodine binding studies revealed that the R4496C mutation resulted in an increase in RyR2 channel activity in particular at low Ca2+ concentrations. This increased basal channel activity remained sensitive to modulation by caffeine, ATP, Mg2+, and ruthenium red. In addition, the R4496C mutation enhanced the sensitivity of RyR2 to activation by Ca2+ and by caffeine. Single-channel analysis showed that single R4496C mutant channels exhibited considerable channel openings at low Ca2+ concentrations. HEK293 cells transfected with mutant R4496C displayed spontaneous Ca2+ oscillations more frequently than cells transfected with wild-type RyR2. Substitution of a negatively charged glutamate for the positively charged R4496 (R4496E) further enhanced the basal channel activity, whereas replacement of R4496 by a positively charged lysine (R4496K) had no significant effect on the basal activity. These observations indicate that the charge and polarity at residue 4496 plays an essential role in RyR2 channel gating. Enhanced basal activity of RyR2 may underlie an arrhythmogenic mechanism for effort-induced ventricular tachycardia.
Key words: ryanodine receptor • Ca2+ release • excitation-contraction coupling • mutations • ventricular arrhythmias
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