2 research outputs found
Nociceptive Sensitizers Are Regulated in Damaged Joint Tissues, Including Articular Cartilage, When Osteoarthritic Mice Display Pain Behavior
OBJECTIVE: Pain is the most common symptom of osteoarthritis (OA), yet where it originates in the joint and how it is driven are unknown. The aim of this study was to identify painâsensitizing molecules that are regulated in the joint when mice subjected to surgical joint destabilization develop OAârelated pain behavior, the tissues in which these molecules are being regulated, and the factors that control their regulation. METHODS: Tenâweekâold mice underwent sham surgery, partial meniscectomy, or surgical destabilization of the medial meniscus (DMM). Painârelated behavior as determined by a variety of methods (testing of responses to von Frey filaments, cold plate testing for cold sensitivity, analgesiometry, incapacitance testing, and forced flexion testing) was assessed weekly. Once painârelated behavior was established, RNA was extracted from either whole joints or microdissected tissue samples (articular cartilage, meniscus, and bone). Reverse transcriptionâpolymerase chain reaction analysis was performed to analyze the expression of 54 genes known to regulate pain sensitization. Cartilage injury assays were performed using avulsed immature hips from wildâtype or genetically modified mice or by explanting articular cartilage from porcine joints preinjected with pharmacologic inhibitors. Levels of nerve growth factor (NGF) protein were measured by enzymeâlinked immunosorbent assay. RESULTS: Mice developed painârelated behavior 8 weeks after undergoing partial meniscectomy or 12 weeks after undergoing DMM. NGF, bradykinin receptors B1 and B2, tachykinin, and tachykinin receptor 1 were significantly regulated in the joints of mice displaying painârelated behavior. Little regulation of inflammatory cytokines, leukocyte activation markers, or chemokines was observed. When tissue samples from articular cartilage, meniscus, and bone were analyzed separately, NGF was consistently regulated in the articular cartilage. The other pain sensitizers were also largely regulated in the articular cartilage, although there were some differences between the 2 models. NGF and tachykinin were strongly regulated by simple mechanical injury of cartilage in vitro in a transforming growth factor βâactivated kinase 1â, fibroblast growth factor 2â, and Src kinaseâdependent manner. CONCLUSION: Damaged joint tissues produce proalgesic molecules, including NGF, in murine OA
Digital Twin Hub: Governance and Trust Working Group : Connected Digital Twin Executive Summary
The Digital Twin (DT) Hub was created in 2020 by the Centre for Digital Britain at the University of Cambridge. In 2022, the DT Hub transitioned to a multi-sector Industry and Catapult Network partnership housed at the Connected Places Catapult. It operates in collaboration with the new National Digital Twin Programme run by the Government's Department for Business, Energy and Industrial Strategy. In order to advance their work, the Hub created four working groups that sought to establish key ambitions, good practice guidance, and showcase events and materials, to support the deployment of digital twins in the UK. This first report by the Governance and Trust working group sets out key understandings and objectives for Digital twins, as they relate to Purpose, Value Creation, and the sustaining of trust in future Connected Digital Twin initiatives