Abstract

Introduction: One approach to the treatment of Type 1 diabetes is the creation of an 'artificial beta cell'. The stable transfection of insulin cDNA into the human liver cell line Huh7 resulted in synthesis, storage and regulated release of insulin to a glucose stimulus (Huh7ins cells). The aim of the present study was to determine if Huh7ins cells respond to glucose via activation of ATP-sensitve potassium channels (KATP) and voltage-gated calcium channels, as is the case with pancreatic beta cells.

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