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DOI 10.1007/s00264-012-1578-6

Медицинская библиотека · International orthopaedics · 2012

Behaviour of human physeal chondro-progenitorcells in early growth plate injury response in vitro.

Pichler Karin, Schmidt Barbara, Fischerauer Eva E, Rinner Beate, Dohr Gottfried, Leithner Andreas, Weinberg Annelie M

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Аннотация

PURPOSE: The aim of this study was to investigate the proliferation and differentiation behaviour of a defined cell population gained from the human growth plate, namely, chondro-progenitorcells (CPCs), in the initial inflammatory phase of growth plate injury response in vitro.

METHODS

Growth plate cells were sorted via FACS and differentiated along adipogenic and osteogenic lineage to confirm their progenitor features. To mimic the inflammatory phase of injury response at the growth plate they were treated with IL-1β and exposed to cyclic mechanical loading. A BrdU assay was used to investigate CPC proliferation. CPC differentiation behaviour was analysed by RT-PCR.

RESULTS

CPCs (CD45-, CD34-, CD73+, CD90+, and CD105+) showed a successful differentiation along adipogenic and osteogenic lineage. Under conditions simulating the inflammatory phase of injury response at the growth plate in vitro CPCs differentiated towards hypertrophy while chondrogenesis and ossification were inhibited. Proliferation was not significantly altered.

CONCLUSION

This study showed that CPCs can be isolated from the human growth plate and expanded in vitro. In the first phase of injury response at the growth plate these cells differentiate towards hypertrophy. As longitudinal growth is obtained by chondrocyte proliferation and volume increase during hypertrophy this maturation might be the first step towards post-traumatic growth disorders such as unwanted premature ossification of the growth plate.

Для цитирования: Pichler Karin, Schmidt Barbara, Fischerauer Eva E, Rinner Beate, Dohr Gottfried, Leithner Andreas, Weinberg Annelie M. Behaviour of human physeal chondro-progenitorcells in early growth plate injury response in vitro.. International orthopaedics. 2012. DOI: 10.1007/s00264-012-1578-6.

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