14.01.2013 Views

Profilaksa DVT kod velikih ortopedskih operacija - Depol ...

Profilaksa DVT kod velikih ortopedskih operacija - Depol ...

Profilaksa DVT kod velikih ortopedskih operacija - Depol ...

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

92<br />

2 st INTERNATIONAL CONFERENCE ON REGENERATIVE ORTHOPAEDICS<br />

CELLULAR AND MOLECULAR ARCHITECTURE OF TENDON AND<br />

LIGAMENT<br />

Andrea Wagner, Paracelsus Medical Universtiy Salzburg, Tendon and Bone Regeneration, Salzburg,<br />

Austria<br />

Renate Gehwolf, Paracelsus Medical Universtiy Salzburg, Tendon and Bone Regeneration, Salzburg,<br />

Austria<br />

Corinna Hirzinger, Universtiy Hospital Salzburg, Traumatology and Sports Injuries, Salzbug, Austria<br />

Milan Toljan, Sportmed Institute, Linz, Austria<br />

Herbert Resch , Universtiy Hospital Salzburg, Traumatology and Sports Injuries, Salzbug, Austria<br />

Hans-Cjristian Bauer, Paracelsus Medical Universtiy Salzburg, Salzburg, Austria<br />

Tendons and ligaments are both dense connective tissues which resemble each other in many aspects but exert<br />

different functions. While the cellular constituents of tendon tissue including tendon progenitor cells have been<br />

well characterized, less information for ligament cells or progenitor cells in ligaments is available. We explore similarities<br />

and differences between tendon and ligament cells at a molecular and biochemical level. Therefore we<br />

used biopsy tissue of semitendinosus tendon (ST) and anterior cruciate ligament (ACL) since ruptured ACL often<br />

is reconstructed by autologous ST grafts.<br />

The expression of progenitor cell markers (Nestin, CD133, Scleraxis) in ACL and ST was analysed by immunhistochemistry<br />

and quantitative RT-PCR. Our analyses revealed differences in the expression levels and expression patterns<br />

of these marker molecules. We also determined the expression of extracellular matrix components (Collagen<br />

type 1, Collagen type 3 and Aggrecan), matrix remodelling proteins (MMP-2, MMP-9, Lysyl oxidase) and Substance<br />

P, a neurotransmitter in pain perception. The mRNA expression of Collagen type 1 and type 3, MMP-2 and Lysyl<br />

oxidase was significantly higher in ACL than in ST. Substance P was only detectable in ACL, Scleraxis and Nestin<br />

showed no differences. The ratio of Collagen type 1 to type 3 mRNA was significantly higher in ACL.<br />

Our results may contribute to the understanding of tendon and ligament nature and origin, and will provide a clue<br />

towards new therapeutic ways in ligament regeneration or reconstruction.<br />

Supported: PMU-FFF E-09/09/051-BAH & ABT GmbH

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!