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. Author manuscript; available in PMC: 2008 Feb 1.
Published in final edited form as: Biochim Biophys Acta. 2006 Oct 3;1773(2):192–200. doi: 10.1016/j.bbamcr.2006.09.031

Fig. 3.

Fig. 3

CFTR-mediated chloride currents across excised membrane patches are reduced by pre-treating BHK-CFTR cells with wiskostatin or latrunculin B. A,B. Representative macroscopic currents recordings for inside-out membrane patches excised from a control BHK-CFTR cell (A) or from a cell pre-treated with 5 μM wiskostatin for 2h (B). Inhibitory PKA peptide (PKI; 1.4 μg/ml) ) was added at the first arrow followed by glibenclamide (250 μM), a voltage-dependent pore blocker. Currents were elicited using a voltage ramp protocol (see Methods). C. Mean glibenclamide-sensitive currents (at −80 mV) for membrane patches excised from control cells and from cells pre-treated for 2h with wiskostatin (5 μM) or latrunculin B (1 μM). Data are means ± S.D. calculated from 4–7 experiments. Asterisk indicates p<0.05 relative to control. ( p = 0.09, for latrunculin B-treated cells)