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. 2017 Apr 11;112(7):1406–1416. doi: 10.1016/j.bpj.2017.01.036

Figure 2.

Figure 2

BK channel is critical in substrate stiffness regulation of L-type Ca2+ channel in ventricular myocytes. (A) Representative whole-cell recordings of Ba2+ currents from cells cultured on the soft and stiff substrates after treatment with 100 nM IBTX for 10 min. (B) Mean I-V relationships from 12 cells in three preparations for each case. (C) Representative whole-cell recordings of Ca2+ currents from cells cultured on the soft and stiff substrates after treatment with 100 nM IBTX for 10 min. (D) Mean I-V relationships from 10 cells in three preparations for each case. (E) Voltage dependence of L-type channel activation determined with tail currents from 12 cells cultured on the soft and stiff substrates after treatment with 100 nM IBTX for 10 min. (F) Voltage dependence of L-type channel inactivation from 12 cells in three preparations on the soft and stiff substrates after treatment with 100 nM IBTX for 10 min.