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Pichler, K; Schmidt, B; Fischerauer, EE; Rinner, B; Dohr, G; Leithner, A; Weinberg, AM.
Behaviour of human physeal chondro-progenitorcells in early growth plate injury response in vitro.
Int Orthop. 2012; 36(9):1961-6 Doi: 10.1007/s00264-012-1578-6 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Pichler Karin
Co-authors Med Uni Graz
Amerstorfer Eva
Dohr Gottfried
Leithner Andreas
Rinner Beate
Schmidt Barbara
Weinberg Annelie-Martina
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Abstract:
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.
Find related publications in this database (using NLM MeSH Indexing)
Adipocytes - drug effects, pathology, physiology
Cell Differentiation - drug effects
Cell Enlargement - drug effects
Cell Proliferation - drug effects
Cell Separation - administration & dosage
Cells, Cultured - administration & dosage
Chondrocytes - drug effects, pathology, physiology
Chondrogenesis - drug effects
Flow Cytometry - administration & dosage
Growth Plate - pathology
Humans - administration & dosage
Interleukin-1beta - pharmacology
Ossification, Heterotopic - chemically induced, pathology, physiopathology
Osteocytes - drug effects, pathology, physiology
Osteogenesis - drug effects
Salter-Harris Fractures - administration & dosage
Stem Cells - drug effects, pathology, physiology
Stress, Mechanical - administration & dosage
Weight-Bearing - administration & dosage

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