AI Article Synopsis

  • Teratoma tumor formation is vital for assessing the pluripotency of human pluripotent stem cells, but there's no consistent testing method currently.
  • A new detailed teratoma assay involves transplanting undifferentiated human embryonic stem cells (hESCs) with inactive feeder cells into immunodeficient mice, showing high efficiency and reproducibility.
  • The assay is sensitive enough to detect teratoma-forming cells even in differentiated cell populations, laying the groundwork for a standardized method for both pluripotency and bio-safety evaluations.

Article Abstract

Teratoma tumor formation is an essential criterion in determining the pluripotency of human pluripotent stem cells. However, currently there is no consistent protocol for assessment of teratoma forming ability. Here we present detailed characterization of a teratoma assay that is based on subcutaneous co-transplantation of defined numbers of undifferentiated human embryonic stem cells (hESCs) with mitotically inactivated feeder cells and Matrigel into immunodeficient mice. The assay was highly reproducible and 100% efficient when 100,000 hESCs were transplanted. It was sensitive, promoting teratoma formation after transplantation of 100 hESCs, though larger numbers of animals and longer follow-up were required. The assay could detect residual teratoma forming cells within differentiated hESC populations however its sensitivity was decreased in the presence of differentiated cells. Our data lay the foundation, for standardization of a teratoma assay for pluripotency analysis. The assay can also be used for bio-safety analysis of pluripotent stem cell-derived differentiated progeny.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458078PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0045532PLOS

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