Identification of insulin-producing cells derived from embryonic stem cells by zinc-chelating dithizone

Stem Cells. 2002;20(4):284-92. doi: 10.1634/stemcells.20-4-284.

Abstract

Background and aims: Embryonic stem (ES) cells have a pluripotent ability to differentiate into a variety of cell lineages in vitro. We have recently identified the emergence of cellular clusters within differentiated ES cell cultures by staining with dithizone (DTZ). DTZ is a zinc-chelating agent known to selectively stain pancreatic beta cells because of their high zinc content. The aim of the present study was to investigate the characteristics of DTZ-stained cellular clusters originating from ES cells.

Methods: Embryoid bodies (EBs), formed by a 5-day hanging drop culture of ES cells, were allowed to form outgrowths in the culture. The outgrowths were incubated in DTZ solution (final concentration, 100 microg/ml ) for 15 minutes before being examined microscopically. The gene expression of endocrine pancreatic markers was also analyzed by reverse transcriptase-polymerase chain reaction. In addition, insulin production was examined immunohistochemically, and its secretion was examined using enzyme-linked immunosorbent assay.

Results: DTZ-stained cellular clusters appeared after approximately 16 days in the EB culture and became more apparent by day 23. They were found to be immunoreactive to insulin and expressed pancreatic-duodenal homeobox 1 (PDX1), proinsulin 1, proinsulin 2, glucagon, pancreatic polypeptide, glucose transporter-2 (GLUT2), and islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP) mRNA. They were also able to secrete detectable amounts of insulin.

Conclusions: ES cell-derived DTZ-positive cellular clusters possess characteristics of the endocrine pancreas, including insulin secretion. Further, DTZ staining is a useful method for the identification of differentiated pancreatic islets developed from EBs in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Cell Separation / methods*
  • Cell Separation / trends
  • Cells, Cultured
  • Chelating Agents*
  • Diabetes Mellitus / therapy*
  • Dithizone*
  • Female
  • Glucose Transporter Type 2
  • Glucose-6-Phosphatase*
  • Immunohistochemistry
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / cytology
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / metabolism
  • Mice
  • Mice, Inbred Strains
  • Monosaccharide Transport Proteins / genetics
  • Proinsulin / genetics
  • Proteins / genetics
  • Stem Cell Transplantation / methods*
  • Stem Cell Transplantation / trends
  • Totipotent Stem Cells / cytology
  • Totipotent Stem Cells / metabolism
  • Totipotent Stem Cells / transplantation*
  • Zinc / metabolism

Substances

  • Chelating Agents
  • Glucose Transporter Type 2
  • Insulin
  • Monosaccharide Transport Proteins
  • Proteins
  • Dithizone
  • Proinsulin
  • Glucose-6-Phosphatase
  • G6pc2 protein, mouse
  • Zinc