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. Author manuscript; available in PMC: 2010 Jan 1.
Published in final edited form as: Cell Calcium. 2008 Jul 11;45(1):29–37. doi: 10.1016/j.ceca.2008.05.006

Table 1.

Effects of junctin/triadin knockdown on stored Ca2+ release in C2C12 myotubes

Addition Control Junctin knockdown Triadin knockdown Junctin/triadin knockdown
10 mM KCl 1.98 ± 0.25 1.61 ± 0.18* 1.49 ± 0.13* 1.27 ± 0.08*
0.4 mM 4-chloro-m-cresol 1.88 ± 0.23 1.65 ± 0.17* 2.05 ± 0.14 1.60 ± 0.11*
10 mM caffeine 1.83 ± 0.17 1.65 ± 0.14* 1.88 ± 0.24 1.69 ± 0.18*
1 μM thapsigargin 1.86 ± 0.17 1.64 ± 0.16* 1.93 ± 0.24 1.63 ± 0.14*
0.4 mM UTP 2.07 ± 0.29 1.46 ± 0.08* 1.90 ± 0.16 1.48 ± 0.07*

Peak values of fluorescence increases (F/F0) in C2C12 myotubes were determined in Fluo-4 loaded cells in Ca2+-free KRH buffer. Data are the mean ± S.E. of 8–17 experiments.

*

p < 0.05 compared to control.