Periostin secreted by mesenchymal stem cells supports tendon formation in an ectopic mouse model.
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Authors
Noack, SandraSeiffart, Virginia
Willbold, Elmar
Laggies, Sandra
Winkel, Andreas
Shahab-Osterloh, Sandra
Flörkemeier, Thilo
Hertwig, Falk
Steinhoff, Christine
Nuber, Ulrike A
Gross, Gerhard
Hoffmann, Andrea
Issue Date
2014-08-15
Metadata
Show full item recordAbstract
True tendon regeneration in human patients remains a vision of musculoskeletal therapies. In comparison to other mesenchymal lineages the biology of tenogenic differentiation is barely understood. Specifically, easy and efficient protocols are lacking that might enable tendon cell and tissue differentiation based on adult (stem) cell sources. In the murine mesenchymal progenitor cell line C3H10T½, overexpression of the growth factor bone morphogenetic protein 2 (BMP2) and a constitutively active transcription factor, Smad8 L+MH2, mediates tendon cell differentiation in vitro and the formation of tendon-like tissue in vivo. We hypothesized that during this differentiation secreted factors involved in extracellular matrix formation exert a major impact on tendon development. Gene expression analyses revealed four genes encoding secreted factors that are notably upregulated: periostin, C-type lectin domain family 3 (member b), RNase A4, and follistatin-like 1. These factors have not previously been implicated in tendon biology. Among these, periostin showed a specific expression in tenocytes of adult mouse Achilles tendon and in chondrocytes within the nonmineralized fibrocartilage zone of the enthesis with the calcaneus. Overexpression of periostin alone or in combination with constitutively active BMP receptor type in human mesenchymal stem cells and subsequent implantation into ectopic sites in mice demonstrated a reproducible moderate tenogenic capacity that has not been described before. Therefore, periostin may belong to the factors contributing to the development of tenogenic tissue.Citation
Periostin secreted by mesenchymal stem cells supports tendon formation in an ectopic mouse model. 2014, 23 (16):1844-57 Stem Cells Dev.Affiliation
1 Department of Orthopaedic Trauma, Hannover Medical School (MHH), Hannover, Germany .Journal
Stem cells and developmentPubMed ID
24809660Type
ArticleLanguage
enISSN
1557-8534ae974a485f413a2113503eed53cd6c53
10.1089/scd.2014.0124
Scopus Count
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