Genetic ablation of adenosine receptor A3 results in articular cartilage degeneration

Osteoarthritis (oa), the most common form of arthritis, is characterized by inflammation of joints and cartilage degradation leading to disability, discomfort, severe pain, inflammation, and stiffness of the joint. it has been shown that adenosine, a purine nucleoside composed of adenine attached to ribofuranose, is enzymatically produced by the human synovium. however, the functional significance of adenosine signaling in homeostasis and pathology of synovial joints remains unclear. adenosine acts through four cell surface receptors, i.e., a1, a2a, a2b, and a3, and here, we have systematically analyzed mice with a deficiency for a3 receptor as well as pharmacological modulations of this receptor with specific analogs. the data show that adenosine receptor signaling plays an essential role in downregulating catabolic mechanisms resulting in prevention of cartilage degeneration. ablation of a3 resulted in development of oa in aged mice. mechanistically, a3 signaling inhibited cellular catabolic processes in chondrocytes including downregulation of ca2+/calmodulin-dependent protein kinase (camkii), an enzyme that promotes matrix degradation and inflammation, as well as runt-related transcription factor 2 (runx2). additionally, selective a3 agonists protected chondrocytes from cell apoptosis caused by pro-inflammatory cytokines or hypo-osmotic stress. these novel data illuminate the protective role of a3, which is mediated via inhibition of intracellular camkii kinase and runx2 transcription factor, the two major pro-catabolic regulators in articular cartilage.