Volume 54, Issue 10 pp. 3254-3266
Research Article

Premature induction of hypertrophy during in vitro chondrogenesis of human mesenchymal stem cells correlates with calcification and vascular invasion after ectopic transplantation in SCID mice

Karoliina Pelttari

Karoliina Pelttari

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

Ms Pelttari and Dr. Winter contributed equally to this work.

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Anja Winter

Anja Winter

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

Ms Pelttari and Dr. Winter contributed equally to this work.

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Eric Steck

Eric Steck

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

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Katrin Goetzke

Katrin Goetzke

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

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Thea Hennig

Thea Hennig

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

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Bjoern Gunnar Ochs

Bjoern Gunnar Ochs

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

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Thomas Aigner

Thomas Aigner

Institute of Pathology, Leipzig, Germany

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Wiltrud Richter

Corresponding Author

Wiltrud Richter

Orthopaedic University Hospital of Heidelberg, Heidelberg, Germany

Division of Experimental Orthopaedics, Orthopaedic Clinic, University of Heidelberg, Schlierbacher Landstrasse 200a, D-69118 Heidelberg, GermanySearch for more papers by this author
First published: 28 September 2006
Citations: 637

Abstract

Objective

Functional suitability and phenotypic stability of ectopic transplants are crucial factors in the clinical application of mesenchymal stem cells (MSCs) for articular cartilage repair, and might require a stringent control of chondrogenic differentiation. This study evaluated whether human bone marrow–derived MSCs adopt natural differentiation stages during induction of chondrogenesis in vitro, and whether they can form ectopic stable cartilage that is resistant to vascular invasion and calcification in vivo.

Methods

During in vitro chondrogenesis of MSCs, the expression of 44 cartilage-, stem cell–, and bone-related genes and the deposition of aggrecan and types II and X collagen were determined. Similarly treated, expanded articular chondrocytes served as controls. MSC pellets were allowed to differentiate in chondrogenic medium for 3–7 weeks, after which the chondrocytes were implanted subcutaneously into SCID mice; after 4 weeks in vivo, samples were evaluated by histology.

Results

The 3-stage chondrogenic differentiation cascade initiated in MSCs was primarily characterized by sequential up-regulation of common cartilage genes. Premature induction of hypertrophy-related molecules (type X collagen and matrix metalloproteinase 13) occurred before production of type II collagen and was followed by up-regulation of alkaline phosphatase activity. In contrast, hypertrophy-associated genes were not induced in chondrocyte controls. Whereas control chondrocyte pellets resisted calcification and vascular invasion in vivo, most MSC pellets mineralized, in spite of persisting proteoglycan and type II collagen content.

Conclusion

An unnatural pathway of differentiation to chondrocyte-like cells was induced in MSCs by common in vitro protocols. MSC pellets transplanted to ectopic sites in SCID mice underwent alterations related to endochondral ossification rather than adopting a stable chondrogenic phenotype. Further studies are needed to evaluate whether a more stringent control of MSC differentiation to chondrocytes can be achieved during cartilage repair in a natural joint environment.

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