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. 2021 Jul 22;22(15):7852. doi: 10.3390/ijms22157852

Figure 7.

Figure 7

Activation of TMEM16A whole-cell currents is potentiated by brevenal. (A) Dose-dependent activation of endogenous TMEM16A whole-cell currents in CFBE airway epithelial cells, by the purinergic agonist ATP. Clamp voltages ± 100 mV in steps of 20 mV. (B) Corresponding current/voltage relationships. (C,D) Activation of whole-cell currents obtained from cells pre-incubated with brevenal (500 nM, 15 min) and corresponding current/voltage relationships. (E) Activation of whole-cell currents in brevenal-incubated cells, in which expression of TMEM16A has been knocked down by treatment with siRNA-TMEM16A (c.f. Supplementary Figure E2). (F) Corresponding current/voltage relationships. Mean ± SEM (number of cells). * significant activation by ATP (p < 0.05, ANOVA). The inhibitor of Ca2+-activated KCNN4 K+ channels, TRAM-34 (100 nM), was present in all patch clamp experiments to avoid potential activation of Ca2+-activated K+ channels. # significant difference when compared to the absence of brevenal (p < 0.05, ANOVA). No currents were activated in siRNA-TMEM16A-treated cells.