Hematoendothelial differentiation of human embryonic stem cells

Curr Protoc Cell Biol. 2007 Sep:Chapter 23:Unit 23.6. doi: 10.1002/0471143030.cb2306s36.

Abstract

Human embryonic stem cells (hESCs) represent a unique population of cells capable of self-renewal and differentiation into all types of somatic cells, including hematopoietic and endothelial cells. Since the pattern of hematopoietic and endothelial development observed in the embryo can be reproduced using ESCs differentiated in culture, hESCs can be used as a model for studies of specification and diversification of hematoendothelial progenitors. In addition, hESCs can be seen as a scalable source of hematopoietic and endothelial cells for in vitro studies. This unit describes a method for efficient differentiation of hESCs into hematopoietic progenitors and endothelial cells through coculture with mouse OP9 bone marrow stromal cells, as well as an approach for their analysis and isolation. Support protocols are provided for culture of mouse embryonic fibroblasts, evaluation of hematopoietic and endothelial differentiation by flow cytometry and colony-forming assay, removal of OP9 cells, and propagation of hESC-derived endothelial cells. Curr. Protoc.

MeSH terms

  • Adult
  • Animals
  • Biomarkers
  • Blood Cells / cytology*
  • Cell Culture Techniques / instrumentation
  • Cell Culture Techniques / methods*
  • Cell Differentiation
  • Cell Separation / methods
  • Cells, Cultured / cytology
  • Cells, Cultured / drug effects
  • Coculture Techniques
  • Colony-Forming Units Assay / methods
  • Culture Media / pharmacology
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / drug effects
  • Endothelial Cells / cytology*
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Flow Cytometry / methods
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Humans
  • Mice
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / drug effects
  • Stromal Cells / cytology
  • Stromal Cells / metabolism

Substances

  • Biomarkers
  • Culture Media