Long-term self-renewal and directed differentiation of human embryonic stem cells in chemically defined conditions Academic Article uri icon

Overview

MeSH Major

  • Cell Culture Techniques
  • Cell Differentiation
  • Culture Media
  • Embryo, Mammalian
  • Stem Cells

abstract

  • Chemically defined medium (CDM) conditions for controlling human embryonic stem cell (hESC) fate will not only facilitate the practical application of hESCs in research and therapy but also provide an excellent system for studying the molecular mechanisms underlying self-renewal and differentiation, without the multiple unknown and variable factors associated with feeder cells and serum. Here we report a simple CDM that supports efficient self-renewal of hESCs grown on a Matrigel-coated surface over multiple passages. Expanded hESCs under such conditions maintain expression of multiple hESC-specific markers, retain the characteristic hESC morphology, possess a normal karyotype in vitro, as well as develop teratomas in vivo. Additionally, several growth factors were found to selectively induce monolayer differentiation of hESC cultures toward neural, definitive endoderm/pancreatic and early cardiac muscle cells, respectively, in our CDM conditions. Therefore, this CDM condition provides a basic platform for further characterization of hESC self-renewal and directed differentiation, as well as the development of novel therapies.

publication date

  • May 2, 2006

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC1458992

Digital Object Identifier (DOI)

  • 10.1073/pnas.0602280103

PubMed ID

  • 16632596

Additional Document Info

start page

  • 6907

end page

  • 12

volume

  • 103

number

  • 18