Why the study?
Does ß-catenin expression upregulate HERG channel activity in Xenopus oocytes?
Does ß-catenin expression upregulate HERG channel activity in Xenopus oocytes?
ß-catenin upregulates HERG channel activity by increasing channel abundance at the cell membrane, independent of transcription.
Hypothesis-generating in Xenopus oocytes; leaves open β-catenin effects on human cardiac repolarization or arrhythmia risk.
The multifunctional protein ß-catenin governs as transcription factor the expression of a wide variety of genes relevant for cell proliferation and cell survival. In addition, ß-catenin is localized at the cell membrane and may influence the function of channels. The present study explored the possibility that ß-catenin participates in the regulation of the HERG K(+) channel. To this end, HERG was expressed in Xenopus oocytes with or without ß-catenin and the voltage-gated current determined utilizing the dual electrode voltage clamp. As a result, expression of ß-catenin markedly upregulated HERG channel activity, an effect not sensitive to inhibition of transcription with actinomycin D (10 µM). According to chemiluminescence, ß-catenin may increase HERG channel abundance within the oocyte cell membrane. Following inhibition of channel insertion into the cell membrane by brefeldin A (5 µM) the decay of current was similar in oocytes expressing HERG together with ß-catenin to oocytes expressing HERG alone. The experiments uncover a novel function of APC/ß-catenin, i.e. the regulation of HERG channels.
No takes yet. Share an insight, caveat, or question.
Muñoz et al. (2012) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: