We propose to identify HA fragments sizes that are useful for promoting wound repair using an assay funnel of 2 D culture screens to identify relevant reagents and then characterize their effects on wound repair using an animal model of excisional skin wounds and human 3D co-culture of skin cells.
Thrombolytic therapy is the mainstay of stroke treatment. However, this treatment can be potentially harmful. A patient-specific model of expected outcome would greatly facilitate the treatment decision making process both for clinicians and patients. We propose to develop a clinical tool by incorporating the imaging and clinical dataset to predict the fate of tissue in ischemic stroke. We expect the product to enable real-time quantification of expected tissue outcomes using patient- and tissue- specific thresholds.
Nowadays, most of cell biomechanics studies based on cell stretching have focused on small stretching magnitude, without the ability to visualize cell behavior and morphology during stretch. We therefor decided to build a cell stretcher/incubator providing the physiological conditions of cell culture (37°C, 5% CO2) while also allowing the application of a wide range of stretching magnitudes. The device consists of a cell stretcher/incubator designed specifically to be mounted on a microscope stage and thus, allows long term (several hours) in situ visualization of cell morphology.
Breast cancer (BC) accounts for 15% of all cancer cases in Ontario, affecting 8,700 women in 2009. Thus, there is a great need for the development of new anti-cancer agents and the identification of patients who are best suited for tailored treatment. The drug metformin has emerged as a potential therapy for BC. Metformin is commonly used to treat type 2 diabetes, but clinical studies have demonstrated that it can inhibit BC. However, it is unclear how metformin inhibits BC and which patients would be most suitable for metformin therapy. Therefore, the goal of the project is to determi
Insulin controls blood sugar and is required for the entry of sugar (glucose) into blood cells from blood. Excess body fat in obesity or high fat diet makes body resistant to insulin. Due to this insulin resistance, sugar accumulates in the blood and over time this leads to an increase in blood sugar and development of type 2 diabetes (T2D). Normally insulin resistance precedes the development of T2D by 10-20 years. Because insulin resistance is associated with cardiovascular problems, people with T2D are at a high risk for heart disease.