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  • Hastoy, B. (author)

Electrophysiological properties of human beta-cell lines EndoC-beta H1 and -beta H2 conform with human beta-cells

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-11-19
  • Springer Science and Business Media LLC,2018

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/273888
  • https://gup.ub.gu.se/publication/273888URI
  • https://doi.org/10.1038/s41598-018-34743-7DOI

Supplementary language notes

  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Limited access to human islets has prompted the development of human beta cell models. The human beta cell lines EndoC-beta H1 and EndoC-beta H2 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 [Ca2+](i), membrane depolarisation and increased action potential firing. Similar to human primary beta cells, K-ATP channel activity is low at 1mM 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 Ca2+ channels with some small contribution of TTX-sensitive Na+ channels. The repolarisation involves activation of voltage-gated Kv2.2 channels and large-conductance Ca2+-activated K+ channels. Exocytosis presented a similar kinetics to human primary beta cells. The ultrastructure of these cells shows insulin vesicles composed of an electrondense core surrounded by a thin clear halo. We conclude that the EndoC-beta H1 and -beta H2 cells share many features of primary human beta-cells and thus represent a useful experimental model.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Godazgar, M. (author)
  • Clark, A. (author)
  • Nylander, V. (author)
  • Spiliotis, I. (author)
  • van de Bunt, M. (author)
  • Chibalina, M. V. (author)
  • Barrett, A. (author)
  • Burrows, C. (author)
  • Tarasov, A. I. (author)
  • Scharfmann, R. (author)
  • Gloyn, A. L. (author)
  • Rorsman, Patrik,1959Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology(Swepub:gu)xrorpa (author)
  • Göteborgs universitetInstitutionen för neurovetenskap och fysiologi, sektionen för fysiologi (creator_code:org_t)

Related titles

  • In:Scientific Reports: Springer Science and Business Media LLC82045-2322

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