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Bioregulation Group: | Immunology & Inflammation | Bone Physiology | Collaboration | Facilities | Members & Research Interests | Equipment
Understanding and manipulating immune responses, inflammation, and bone
turnover will lead to more effective treatment of numerous conditions, including
infectious diseases, chronic inflammatory diseases (arthritis and periodontitis),
autoimmune diseases (multiple sclerosis and insulin-dependent diabetes),
metabolic bone diseases (osteoporosis), malocclusions, abnormal craniofacial
development and cancer. Secreted cytokines and cell surface receptors regulate
the immune system, bone-turnover and tissue repair. It is, therefore, critical
to identify these cytokines and their receptors, as well as their genes,
promoter sequences, and associated transcription factors. Discovery of novel
cytokines, synthetic analogues, or blocking agents that improve the course
of the inflammatory, immune and bone responses will be more predictable
using this information.
Human model protocols used by the Bioregulation Group (BRG) in these
endeavors are of three main types:
- experimental bone turnover caused by controlled tooth movement
- chronic inflammation caused by natural accumulation of bacteria in
the gingival crevice, or micro-wounding
- regulation of cytokine expression in cells of the immune system and
bone microenvironment, including the impact of dramatic changes in the
systemic endocrine systems, such as estrogen deficiency in menopause
Cytokine production and modulation are currently studied in vivo using harvested
tissues and exudates from specific microenvironments, and in vitro using
cell and bone cultures. Modulating factors being investigated include endotoxin
and other bacterial products, tobacco products, estrogen, antibiotics, nonantibacterial
tetracyclines, and nonsteroidal anti-inflammatory drugs.
Rodent model protocols used include:
- investigation of costimulatory factors and other mechanisms by which
cytokine profiles are regulated
- effects of cytokines and growth factors (rodent and human) on in vivo
bone growth and resorption
- characterization of signalling pathways for the expression of cytokines
and inducible nitric oxide synthase in glial cells and spinal cord of
experimental allergic encephalomyelitis (animal model for multiple sclerosis)
- effects of topical drugs (e.g. simvastatin) and anti-inflamatory agents
on bone growth in a bilateral rat mandible model.
Last modified:
April 2, 2007 6:14 PM