Searchable abstracts of presentations at key conferences on calcified tissues

ba0001pp56 | Bone biomechanics and quality | ECTS2013

Quantitative assessment of bone remodelling and osteophytogenesis in murine osteoarthritis

Borges Patricia , Vincent Tonia , Marenzana Massimo

Subchondral bone remodelling and osteophyte growth are widely recognised hallmarks of knee osteoarthritis (OA) although their contribution to disease is not fully understood. Murine models, with targeted genetic modifications, have become powerful tools for discovering disease pathophysiology. Our unpublished observations suggest that osteophyte formation is independent of cartilage loss thereby implying potentially independent molecular drivers. We have developed a novel imag...

ba0003pp20 | Bone biomechanics and quality | ECTS2014

Subchondral bone sclerosis in the DMM model of murine OA is not associated with changes in either BMD or nanomechanical properties

Borges Patricia Das Neves , Vincent Tonia L , Oyen Michelle L , Marenzana Massimo

It has long been known that osteoarthritis induces dramatic structural changes in subchondral bone. Studies on patientsÂ’ biopsies have also shown that the new sclerotic bone is hypomineralized and has decreased elastic modulus. Due to their amenability for genetic studies, murine models of OA are particularly important for drug target discovery. However, whilst osteosclerosis has been reported also in murine OA models, little is known about the compositional and mechanica...

ba0005oc6.6 | Development and differentiation (or Aging) | ECTS2016

Loss of the longevity gene SirT1 dysregulates chondrocytes and leads to an arthritic phenotype in vivo, via impaired autophagy

Sacitharan Pradeep Kumar , Zarebska Jadwiga , Gharios George Bou , Vincent Tonia , Edwards James

Ageing is universally linked to skeletal deterioration. Common mechanisms may control both processes, where dysregulation may predispose to bone loss and osteoarthritis (OA). The epigenetic modifier SirT1 controls lifespan and decreases with age. However, the role of SirT1 in joint disease is unclear. Human tissue samples, novel genetically modified mice, a surgical disease model and advanced cellular and molecular studies were employed to explore the hypothesis that SirT1 is ...