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Limited access to human islets has prompted the development of human beta cell models. The human beta cell lines EndoC-βH1 and EndoC-βH2 are increasingly used by the research community. However, little is known of their electrophysiological and secretory properties. Here, we monitored parameters that constitute the glucose-triggering pathway of insulin release. Both cell lines respond to glucose (6 and 20 mM) with 2- to 3-fold stimulation of insulin secretion which correlated with an elevation of [Ca 2+ ] i , membrane depolarisation and increased action potential firing. Similar to human primary beta cells, K ATP  channel activity is low at 1 mM glucose and is further reduced upon increasing glucose concentration; an effect that was mimicked by the K ATP  channel blocker tolbutamide. The upstroke of the action potentials reflects the activation of Ca 2+  channels with some small contribution of TTX-sensitive Na +  channels. The repolarisation involves activation of voltage-gated Kv2.2 channels and large-conductance Ca 2+ -activated K +  channels. Exocytosis presented a similar kinetics to human primary beta cells. The ultrastructure of these cells shows insulin vesicles composed of an electron-dense core surrounded by a thin clear halo. We conclude that the EndoC-βH1 and -βH2 cells share many features of primary human β-cells and thus represent a useful experimental model.

Electrophysiological properties of human beta-cell lines EndoC-βH1 and -βH2 conform with human beta-cells