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Virgin β-Cells at the Neogenic Niche Proliferate Normally and Mature Slowly.

Sharon LeeJing ZhangSupraja SaravanakumarMarcus F FlisherDavid R GrimmTalitha van der MeulenMark O Huising
Published in: Diabetes (2021)
Proliferation of pancreatic β-cells has long been known to reach its peak in the neonatal stages and decline during adulthood. However, β-cell proliferation has been studied under the assumption that all β-cells constitute a single, homogenous population. It is unknown whether a subpopulation of β-cells retains the capacity to proliferate at a higher rate and thus contributes disproportionately to the maintenance of mature β-cell mass in adults. We therefore assessed the proliferative capacity and turnover potential of virgin β-cells, a novel population of immature β-cells found at the islet periphery. We demonstrate that virgin β-cells can proliferate but do so at rates similar to those of mature β-cells from the same islet under normal and challenged conditions. Virgin β-cell proliferation rates also conform to the age-dependent decline previously reported for β-cells at large. We further show that virgin β-cells represent a long-lived, stable subpopulation of β-cells with low turnover into mature β-cells under healthy conditions. Our observations indicate that virgin β-cells at the islet periphery can divide but do not contribute disproportionately to the maintenance of adult β-cell mass.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • cell proliferation
  • endoplasmic reticulum stress
  • signaling pathway
  • stem cells
  • cell death
  • mesenchymal stem cells
  • bone marrow
  • climate change
  • postmenopausal women
  • early life