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. 2009 Oct 21;298(1):C149–C162. doi: 10.1152/ajpcell.00241.2009

Fig. 2.

Fig. 2.

Store-operated entry of Ca2+ in muscle fibers from TRPC1+/+ and TRPC1−/− mice. A and B: Ca2+ release from the stores was triggered by stimulation with 20 mM caffeine and 1 μM thapsigargin (Tg) in the presence of 1 mM Mn2+. This induced an increase of intracellular Ca2+ concentration ([Ca2+]i) (reflected by an increase of the fluorescence ratio F340/F360; B) and an increase of Ca2+ entry (reflected by an increase of the quenching rate of fura-PE3 by Mn2+; A). C: comparison of fura-PE3 quenching rates by Mn2+ at rest (gray bars) and after Ca2+ release induced by caffeine and Tg stimulation (black bars representing difference between fura-PE3 quenching rates after and before stimulation) in muscle fibers from TRPC1+/+ (n = 13) and TRPC1−/− mice (n = 14). Results are means ± SE.