The overall purpose of our research is to understand how glucose stimulates insulin secretion by pancreatic islet cells and to characterize and reverse abnormalities in this process that are present in diabetes. Insulin secretion by pancreatic islets is very tightly coupled to changes in the blood glucose; abnormalities in insulin secretion are a major factor in both type 1 and type 2 diabetes. Our research utilizes a variety of research approaches including RNA and protein analysis, genetically modified mice, in vivo physiology, radioimmunoassay, adenovirus mediated gene transfer, transplantation of murine and human islets, confocal microscopy, and immunocytochemistry and involves collaborations with vascular biologists, development biologists, biomedical engineers, and transplant biologists.
More information is available on our lab's website:
7465 Medical Research Bldg IV
2215 Garland Avenue
Nashville, TN 37232-0475
(615) 936-7678 (p)
(615) 936-0063 (f)
MeSH terms are retrieved from PubMed records. Learn more.
Key: MeSH Term KeywordAdult Animals, Laboratory Brain Chickens diabetes Gene Expression Profiling Genes, Reporter Glucagon Glucagon-Secreting Cells Glucose GSIS Image Interpretation, Computer-Assisted imaging insulin islets Islets of Langerhans MafB Transcription Factor Mice, Inbred NOD Mitochondrial Proteins Paired Box Transcription Factors pancreas Pancreas Pancreatitis PAX6 Transcription Factor Recombinant Fusion Proteins regeneration Regional Blood Flow Signal Transduction Species Specificity Spectrometry, Fluorescence Superoxide Dismutase Time Factors Tissue Preservation Tomography, X-Ray Computed Trans-Activators vascularization Whole Body Imaging Zebrafish