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Virgin Beta Cells Persist throughout Life at a Neogenic Niche within Pancreatic Islets.

Cell metabolism | 2017

Postnatal maintenance or regeneration of pancreatic beta cells is considered to occur exclusively via the replication of existing beta cells, but clinically meaningful restoration of human beta cell mass by proliferation has never been achieved. We discovered a population of immature beta cells that is present throughout life and forms from non-beta precursors at a specialized micro-environment or "neogenic niche" at the islet periphery. These cells express insulin, but lack other key beta cell markers, and are transcriptionally immature, incapable of sensing glucose, and unable to support calcium influx. They constitute an intermediate stage in the transdifferentiation of alpha cells to cells that are functionally indistinguishable from conventional beta cells. We thus identified a lifelong source of new beta cells at a specialized site within healthy islets. By comparing co-existing immature and mature beta cells within healthy islets, we stand to learn how to mature insulin-expressing cells into functional beta cells.

Pubmed ID: 28380380 RIS Download

Research resources used in this publication

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: P30 CA093373
  • Agency: NCRR NIH HHS, United States
    Id: S10 RR026825
  • Agency: NIDDK NIH HHS, United States
    Id: UC4 DK116271
  • Agency: NIDDK NIH HHS, United States
    Id: U01 DK089529
  • Agency: NIDDK NIH HHS, United States
    Id: UC4 DK104119
  • Agency: NCRR NIH HHS, United States
    Id: C06 RR012088

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This is a list of tools and resources that we have found mentioned in this publication.


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