A window in time for β-cell regeneration

Genes Dev. 2020 Dec 1;34(23-24):1559-1561. doi: 10.1101/gad.345769.120.

Abstract

In vivo regeneration of β cells provides hope for self-renewal of functional insulin-secreting cells following β-cell failure, a historically fatal condition now sustainable only by administration of exogenous insulin. Despite advances in the treatment of diabetes mellitus, the path toward endogenous renewal of β-cell populations has remained elusive. Intensive efforts have focused on elucidating pancreatic transcriptional programs that can drive the division and (trans-)differentiation of non-β cells to produce insulin. A surprise has been the identification of an essential role of the molecular circadian clock in the regulation of competent insulin-producing β cells. In this issue of Genes & Development, work by Petrenko and colleagues (pp. 1650-1665) now shows a requirement for the intrinsic clock in the regenerative capacity of insulin-producing cells following genetic ablation of β cells. These studies raise the possibility that enhancing core clock activity may provide an adjuvant in cell replacement therapies.

Keywords: Insulin-rtTA/TET-DTA mouse model; circadian clockwork; diabetes; glucose metabolism; pancreatic α and β cells; β-cell proliferation; β-cell regeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review
  • Comment

MeSH terms

  • Circadian Clocks*
  • Diabetes Mellitus*
  • Humans
  • Insulin
  • Insulin-Secreting Cells*
  • Pancreas

Substances

  • Insulin