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Specification of chondrocytes and cartilage tissues from embryonic stem cells.

Publication ,  Journal Article
Craft, AM; Ahmed, N; Rockel, JS; Baht, GS; Alman, BA; Kandel, RA; Grigoriadis, AE; Keller, GM
Published in: Development
June 2013

Osteoarthritis primarily affects the articular cartilage of synovial joints. Cell and/or cartilage replacement is a promising therapy, provided there is access to appropriate tissue and sufficient numbers of articular chondrocytes. Embryonic stem cells (ESCs) represent a potentially unlimited source of chondrocytes and tissues as they can generate a broad spectrum of cell types under appropriate conditions in vitro. Here, we demonstrate that mouse ESC-derived chondrogenic mesoderm arises from a Flk-1(-)/Pdgfrα(+) (F(-)P(+)) population that emerges in a defined temporal pattern following the development of an early cardiogenic F(-)P(+) population. Specification of the late-arising F(-)P(+) population with BMP4 generated a highly enriched population of chondrocytes expressing genes associated with growth plate hypertrophic chondrocytes. By contrast, specification with Gdf5, together with inhibition of hedgehog and BMP signaling pathways, generated a population of non-hypertrophic chondrocytes that displayed properties of articular chondrocytes. The two chondrocyte populations retained their hypertrophic and non-hypertrophic properties when induced to generate spatially organized proteoglycan-rich cartilage-like tissue in vitro. Transplantation of either type of chondrocyte, or tissue generated from them, into immunodeficient recipients resulted in the development of cartilage tissue and bone within an 8-week period. Significant ossification was not observed when the tissue was transplanted into osteoblast-depleted mice or into diffusion chambers that prevent vascularization. Thus, through stage-specific manipulation of appropriate signaling pathways it is possible to efficiently and reproducibly derive hypertrophic and non-hypertrophic chondrocyte populations from mouse ESCs that are able to generate distinct cartilage-like tissue in vitro and maintain a cartilage tissue phenotype within an avascular and/or osteoblast-free niche in vivo.

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Published In

Development

DOI

EISSN

1477-9129

Publication Date

June 2013

Volume

140

Issue

12

Start / End Page

2597 / 2610

Location

England

Related Subject Headings

  • Time Factors
  • Signal Transduction
  • Receptor, Platelet-Derived Growth Factor alpha
  • Osteogenesis
  • Osteoblasts
  • Mice
  • Mesoderm
  • Immunohistochemistry
  • Hypertrophy
  • Growth Differentiation Factor 5
 

Citation

APA
Chicago
ICMJE
MLA
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Craft, A. M., Ahmed, N., Rockel, J. S., Baht, G. S., Alman, B. A., Kandel, R. A., … Keller, G. M. (2013). Specification of chondrocytes and cartilage tissues from embryonic stem cells. Development, 140(12), 2597–2610. https://doi.org/10.1242/dev.087890
Craft, April M., Nazish Ahmed, Jason S. Rockel, Gurpreet S. Baht, Benjamin A. Alman, Rita A. Kandel, Agamemnon E. Grigoriadis, and Gordon M. Keller. “Specification of chondrocytes and cartilage tissues from embryonic stem cells.Development 140, no. 12 (June 2013): 2597–2610. https://doi.org/10.1242/dev.087890.
Craft AM, Ahmed N, Rockel JS, Baht GS, Alman BA, Kandel RA, et al. Specification of chondrocytes and cartilage tissues from embryonic stem cells. Development. 2013 Jun;140(12):2597–610.
Craft, April M., et al. “Specification of chondrocytes and cartilage tissues from embryonic stem cells.Development, vol. 140, no. 12, June 2013, pp. 2597–610. Pubmed, doi:10.1242/dev.087890.
Craft AM, Ahmed N, Rockel JS, Baht GS, Alman BA, Kandel RA, Grigoriadis AE, Keller GM. Specification of chondrocytes and cartilage tissues from embryonic stem cells. Development. 2013 Jun;140(12):2597–2610.
Journal cover image

Published In

Development

DOI

EISSN

1477-9129

Publication Date

June 2013

Volume

140

Issue

12

Start / End Page

2597 / 2610

Location

England

Related Subject Headings

  • Time Factors
  • Signal Transduction
  • Receptor, Platelet-Derived Growth Factor alpha
  • Osteogenesis
  • Osteoblasts
  • Mice
  • Mesoderm
  • Immunohistochemistry
  • Hypertrophy
  • Growth Differentiation Factor 5