Figure 3.
Figure 3. The effect of low extracellular [Ca2+]i (50 nM) and thapsigargin on the APC-induced [Ca2+]i signal. (A) BECs in media containing 1.8 mM or 50 nM Ca2+ were subjected to APC (100 nM) perfusions. Traces represent [Ca2+]i of 12 to 15 single cells from a representative experiment. Horizontal line indicates the time of APC addition. (B) Thapsigargin (1 μM; TG) was introduced to BEC culture as indicated by the horizontal line, and APC (100 nM) was administered for 60 seconds at the time indicated by the arrow. Traces show [Ca2+]i in single cells from representative experiments.

The effect of low extracellular [Ca2+]i (50 nM) and thapsigargin on the APC-induced [Ca2+]i signal. (A) BECs in media containing 1.8 mM or 50 nM Ca2+ were subjected to APC (100 nM) perfusions. Traces represent [Ca2+]i of 12 to 15 single cells from a representative experiment. Horizontal line indicates the time of APC addition. (B) Thapsigargin (1 μM; TG) was introduced to BEC culture as indicated by the horizontal line, and APC (100 nM) was administered for 60 seconds at the time indicated by the arrow. Traces show [Ca2+]i in single cells from representative experiments.

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