Skip to main content
. 2006 Aug 24;116(9):2510–2520. doi: 10.1172/JCI29128

Figure 4. Casq2–/– myocytes display spontaneous Ca2+ releases and triggered beats but largely maintain normal contractility, SR Ca2+ release amplitudes, and SR Ca2+ content.

Figure 4

(A) Examples of [Ca2+]i transients (top traces) and cell shortening (bottom traces) recorded from fura-2/AM–loaded, field-stimulated myocytes (1 Hz). Application of 1 μmol/l isoproterenol (ISO) significantly increased Ca2+ transients and cell shortening in both myocytes. Note that shortly after ISO application was started, only the Casq2–/–myocyte displayed spontaneous Ca2+ releases and aftercontractions of increasing amplitude following each paced twitch (vertical lines). (B and C) Comparison of the incidence of spontaneous (Spont.) Ca2+ release events (B) and Ca2+ oscillations (C) at baseline and in the presence of ISO. Data represent the fraction (%) of myocytes that displayed at least 1 event during a 20-second recording period. Insets show representative examples of spontaneous Ca2+ after-releases (arrows in B, inset) and Ca2+ oscillations (C, inset) induced by spontaneous Ca2+ releases and triggered beats (# in C, inset). *P < 0.05, **P < 0.01, P < 0.001, Casq2–/– versus Casq2+/+ myocytes by Fisher’s exact test. Casq2+/+ myocytes: n = 45 (baseline) and 27 (ISO); Casq2–/–myocytes: n = 71 (baseline) and 43 (ISO).