Behaviour of human physeal chondro-progenitorcells in early growth plate injury response in vitro View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2012-05-25

AUTHORS

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

ABSTRACT

PurposeThe 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.MethodsGrowth 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.ResultsCPCs (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.ConclusionThis 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. More... »

PAGES

1961-1966

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00264-012-1578-6

DOI

http://dx.doi.org/10.1007/s00264-012-1578-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1010297607

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22627866


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