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Progression of Gene Expression Changes following a Mechanical Injury to Articular Cartilage as a Model of Early Stage Osteoarthritis.
McCulloch, R S; Ashwell, M S; Maltecca, C; O'Nan, A T; Mente, P L.
Afiliação
  • McCulloch RS; Joint Department of Biomedical Engineering, North Carolina State University, Raleigh, NC 27695, USA ; University of North Carolina, Chapel Hill, NC 27599, USA ; Human Physiology Department, Gonzaga University, Spokane, WA 99258, USA.
  • Ashwell MS; Department of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
  • Maltecca C; Department of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
  • O'Nan AT; Department of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
  • Mente PL; Joint Department of Biomedical Engineering, North Carolina State University, Raleigh, NC 27695, USA ; University of North Carolina, Chapel Hill, NC 27599, USA.
Arthritis ; 2014: 371426, 2014.
Article em En | MEDLINE | ID: mdl-25478225
An impact injury model of early stage osteoarthritis (OA) progression was developed using a mechanical insult to an articular cartilage surface to evaluate differential gene expression changes over time and treatment. Porcine patellae with intact cartilage surfaces were randomized to one of three treatments: nonimpacted control, axial impaction (2000 N), or a shear impaction (500 N axial, with tangential displacement to induce shear forces). After impact, the patellae were returned to culture for 0, 3, 7, or 14 days. At the appropriate time point, RNA was extracted from full-thickness cartilage slices at the impact site. Quantitative real-time PCR was used to evaluate differential gene expression for 18 OA related genes from four categories: cartilage matrix, degradative enzymes and inhibitors, inflammatory response and signaling, and cell apoptosis. The shear impacted specimens were compared to the axial impacted specimens and showed that shear specimens more highly expressed type I collagen (Col1a1) at the early time points. In addition, there was generally elevated expression of degradative enzymes, inflammatory response genes, and apoptosis markers at the early time points. These changes suggest that the more physiologically relevant shear loading may initially be more damaging to the cartilage and induces more repair efforts after loading.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2014 Tipo de documento: Article