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Artifactual Insulin Release From Differentiated Embryonic Stem Cells

  1. Mattias Hansson1,
  2. Anna Tonning2,
  3. Ulrik Frandsen1,
  4. Andreas Petri13,
  5. Jayaraj Rajagopal4,
  6. Mikael C.O. Englund5,
  7. R. Scott Heller1,
  8. Joakim Håkansson2,
  9. Jan Fleckner3,
  10. Helen Nilsson Sköld2,
  11. Douglas Melton4,
  12. Henrik Semb2 and
  13. Palle Serup1
  1. 1Department of Developmental Biology, Hagedorn Research Institute, Gentofte, Denmark
  2. 2Department of Medical Biochemistry, Göteborg University, Göteborg, Sweden
  3. 3Department of Molecular Genetics, Novo Nordisk A/S, Bagsvaerd, Denmark
  4. 4Department of Molecular and Cellular Biology, Howard Hughes Medical Institute, Harvard University, Cambridge, Massachusetts
  5. 5Cell Therapeutics Scandinavia, Göteborg, Sweden
  1. Address correspondence and reprint requests to Palle Serup, Ph.D., Department of Developmental Biology, Hagedorn Research Institute, Niels Steensens vej 6, DK-2820 Gentofte, Denmark. E-mail: pas{at}hagedorn.dk. Or to Henrik Semb, Section for Endocrinology, Lunds University, Lund, Sweden. E-mail: henrik.semb{at}endo.mas.lu.se

Abstract

Several recent reports claim the generation of insulin-producing cells from embryonic stem cells via the differentiation of progenitors that express nestin. Here, we investigate further the properties of these insulin-containing cells. We find that although differentiated cells contain immunoreactive insulin, they do not contain proinsulin-derived C-peptide. Furthermore, we find variable insulin release from these cells upon glucose addition, but C-peptide release is never detected. In addition, many of the insulin-immunoreactive cells are undergoing apoptosis or necrosis. We further show that cells cultured in the presence of a phosphoinositide 3-kinase inhibitor, which previously was reported to facilitate the differentiation of insulin+ cells, are not C-peptide immunoreactive but take up fluorescein isothiocyanate–labeled insulin from the culture medium. Together, these data suggest that nestin+ progenitor cells give rise to a population of cells that contain insulin, not as a result of biosynthesis but from the uptake of exogenous insulin. We conclude that C-peptide biosynthesis and secretion should be demonstrated to claim insulin production from embryonic stem cell progeny.

Footnotes

  • M.H., A.T., and U.F. contributed equally to this work.

    H.S.’s current affiliation is with the Section for Endocrinology, Lunds University, Lund, Sweden. U.F.’s current affiliation is with Odense University Hospital, Clinical Molecular Endocrinology, Odense, Denmark.

    • Accepted July 1, 2004.
    • Received March 18, 2004.
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