PUBLICATION

Insulin-producing β-cells regenerate ectopically from a mesodermal origin under the perturbation of hemato-endothelial specification

Authors
Liu, K.C., Villasenor, A., Bertuzzi, M., Schmitner, N., Radros, N., Rautio, L., Mattonet, K., Matsuoka, R.L., Reischauer, S., Stainier, D.Y., Andersson, O.
ID
ZDB-PUB-210818-9
Date
2021
Source
eLIFE   10: (Journal)
Registered Authors
Liu, Ka-Cheuk, Matsuoka, Ryota, Reischauer, Sven, Stainier, Didier
Keywords
beta-cell regeneration, cellular origin, developmental biology, differentiation, ectopic beta-cells, regenerative medicine, stem cells, zebrafish
MeSH Terms
  • Animals
  • Cell Differentiation*
  • Endothelium/physiology
  • Insulin-Secreting Cells/physiology*
  • Insulins/metabolism
  • Mesoderm/embryology*
  • Regeneration*
  • Zebrafish/embryology*
  • Zebrafish/physiology
PubMed
34403334 Full text @ Elife
Abstract
To investigate the role of the vasculature in pancreatic β-cell regeneration, we crossed a zebrafish β-cell ablation model into the avascular npas4l mutant (i.e. cloche). Surprisingly, β-cell regeneration increased markedly in npas4l mutants owing to the ectopic differentiation of β-cells in the mesenchyme, a phenotype not previously reported in any models. The ectopic β-cells expressed endocrine markers of pancreatic β-cells, and also responded to glucose with increased calcium influx. Through lineage tracing, we determined that the vast majority of these ectopic β-cells has a mesodermal origin. Notably, ectopic β-cells were found in npas4l mutants as well as following knockdown of the endothelial/myeloid determinant Etsrp. Together, these data indicate that under the perturbation of endothelial/myeloid specification, mesodermal cells possess a remarkable plasticity enabling them to form β-cells, which are normally endodermal in origin. Understanding the restriction of this differentiation plasticity will help exploit an alternative source for β-cell regeneration.
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