4.7 Article

Connexin 43 Functions as a Positive Regulator of Stem Cell Differentiation into Definitive Endoderm and Pancreatic Progenitors

期刊

ISCIENCE
卷 19, 期 -, 页码 450-+

出版社

CELL PRESS
DOI: 10.1016/j.isci.2019.07.033

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资金

  1. WA State Life Sciences Discovery Fund Program Grant [4553677]
  2. Innovation Pilot Award from the UW Institute for Stem Cell and Regenerative Medicine
  3. State of Washington
  4. Pharm. Sci. Training grant [5T32GM007750-34]
  5. Diabetes Research Connection
  6. Howard Hughes Medical Institute (Med-Into-Grad program) [56006778]
  7. Tom and Sue Ellison Stem Cell Core
  8. [R01 DK103711]
  9. [R01GM055632]
  10. [RO1 HL075270]
  11. [R01 DK114693]

向作者/读者索取更多资源

Efficient stem cell differentiation into pancreatic islet cells is of critical importance for the development of cell replacement therapies for diabetes. Here, we identify the expression pattern of connexin 43 (Cx43), a gap junction (GJ) channel protein, in human embryonic stem cell (hESC)-derived definitive endoderm (DE) and primitive gut tube cells, representing early lineages for posterior foregut (PF), pancreatic progenitors (PP), pancreatic endocrine progenitors (PE), and islet cells. As the function of GJ channels is dependent on their gating status, we tested the impact of supplementing hESC-derived PP cell cultures with AAP10, a peptide that promotes Cx43 GJ channel opening. We found that this treatment promotes the expression of DE markers FoxA2 and Sox17, leads to a more efficient derivation of DE, and improves the yield of PF, PP, and PE cells. These results demonstrate a functional involvement of GJ channels in the differentiation of embryonic stem cells into pancreatic cell lineages.

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