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. 2010 Feb 26;393(1):50–54. doi: 10.1016/j.bbrc.2010.01.074

Fig. 3.

Fig. 3

Pb2+ inhibits TRPM2 and TRPM3 channels. Data from multiwell [Ca2+]i measurement from T-rex HEK 293 cells. (A) Mean response from three independent experiments for change in [Ca2+]i in response to Pb2+ (10 μM), and H2O2 (1 mM) in cells with TRPM2 over-expression. (B) Example time-series graph for [Ca2+]i in response to H2O2 (1 mM) in cells with TRPM2 over-expression incubated for 15 min in SBS with or without Pb2+ (10 μM). The data points represent the mean ± SEM for three wells. (C) As of (B) but showing the mean data for three independent experiments. (tet+, induced TRPM2 cells; tet−, control cells.) (D) Mean response from three independent experiments for change in [Ca2+]i in response to Pb2+ (10 μM), and pregnenolone sulphate (PregS; 10 μM) in cells with TRPM3 over-expression. (E) Example time-series graph for [Ca2+]i in response to PregS (10 μM) in cells with TRPM3 over-expression incubated for 15 min in SBS with or without Pb2+ (10 μM). The data points represent the mean ± SEM for three wells. (F) As of (E) but showing the mean data for three independent experiments. (tet+, induced TRPM3 cells; tet−, control cells.)