Derivation and Chondrogenic Commitment of Human Embryonic Stem Cell-Derived Mesenchymal Progenitors

Methods Mol Biol. 2015:1340:65-78. doi: 10.1007/978-1-4939-2938-2_5.

Abstract

The induction of human embryonic stem cells to a mesenchymal-like progenitor population constitutes a developmentally relevant approach for efficient directed differentiation of human embryonic stem (hES) cells to the chondrogenic lineage. The initial enrichment of a hemangioblast intermediate has been shown to yield a replenishable population of highly purified progenitor cells that exhibit the typical mesenchymal stem cell (MSC) surface markers as well as the capacity for multilineage differentiation to bone, fat, and cartilage. Herein, we provide detailed methodologies for the derivation and characterization of potent mesenchymal-like progenitors from hES cells and describe in vitro assays for bone morphogenetic protein (BMP)-2-mediated differentiation to the chondrogenic lineage.

Keywords: BMP-2; Chondrogenic differentiation; Hemangioblast; Human embryonic stem cells; Mesenchymal stem cells; Pellet culture.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Bone Morphogenetic Protein 2 / pharmacology
  • Cell Differentiation
  • Cell Lineage
  • Cell Separation
  • Chondrocytes / drug effects
  • Chondrocytes / metabolism
  • Chondrocytes / physiology*
  • Chondrocytes / transplantation
  • Chondrogenesis* / drug effects
  • Chondrogenesis* / genetics
  • Coculture Techniques
  • Embryonic Stem Cells / drug effects
  • Embryonic Stem Cells / metabolism
  • Embryonic Stem Cells / physiology*
  • Embryonic Stem Cells / transplantation
  • Feeder Cells
  • Flow Cytometry
  • Gene Expression Regulation, Developmental
  • Humans
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / physiology*
  • Mice
  • Phenotype
  • Regenerative Medicine / methods*
  • Tissue Engineering / methods*
  • Tissue Scaffolds

Substances

  • BMP2 protein, human
  • Biomarkers
  • Bone Morphogenetic Protein 2