Glucocorticoid treatment independently affects expansion and transdifferentiation of porcine neonatal pancreas cell clusters

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10 Scopus citations

Abstract

The purpose of this study was to determine the effects of duration and timing of glucocorticoid treatment on the expansion and differentiation of porcine neonatal pancreas cell clusters (NPCCs) into β-cells. After transplantation of NPCCs, the ductal cyst area and β-cell mass in the grafts both showed positive and negative correlations with duration of dexamethasone (Dx) treatment. Pdx-1 and HNF-3β gene expression was significantly downregulated following Dx treatment, whereas PGC-1α expression increased. Pancreatic duct cell apoptosis significantly increased following Dx treatment, whereas proliferation did not change. Altogether, transdifferentiation of porcine NPCCs into β-cells was influenced by the duration of Dx treatment, which might have been due to the suppression of key pancreatic transcription factors. PGC-1α plays an important role in the expansion and transdifferentiation of porcine NPCCs, and the initial 2 weeks following transplantation of porcine NPCCs is a critical period in determining the final β-cell mass in grafts.

Original languageEnglish
Pages (from-to)51-56
Number of pages6
JournalBMB Reports
Volume45
Issue number1
DOIs
StatePublished - Jan 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Dexamethasone (Dx)
  • Diabetes mellitus
  • Neonatal porcine pancreas cell clusters (NPCCs)
  • Pancreatic β-cells
  • Transdifferentiation

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