Beta-Cell Mass And Function In Implants and Pancreas
Beta-Cell Mass And Function In Implants and Pancreas
批准号:
6576257
负责人:
Wen-hong Li
金额:
$14.48万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-30 至 2004-08-31
关键词:
bioimaging /biomedical imaging biomarker cell population study diabetes mellitus diabetes mellitus therapy genetically modified animals insulin laboratory mouse laboratory rat leptin magnetic resonance imaging membrane permeability method development noninvasive diagnosis pancreas pancreas imaging /visualization pancreatic islet function pancreatic islet transplantation pancreatic islets reagent /indicator receptor expression tissue /cell culture
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Beta-cells of the islets of Langerhans play important roles in regulating metabolism through the action of secreting insulin. In type 1diabetes, beta cells are quickly damaged or destroyed. In type 2 diabetes, beta-cells appear to be gradually injured over a prolonged period. However, the details of this injury process are poorly understood, in part because we have no method to localize beta-cells in vivo. Attempts to treat diabetes by introducing beta-cells are also limited in part by uncertainty about the fate of the cells. This proposed technology development project is designed to demonstrate new methods of imaging beta-cellls in vivo. We have synthesized novel magnetic resonance imaging (MRI) contrast agents that can diffuse inside cells and accumulate to high concentrations. Preliminary studies suggested that labeled beta-cells grew and secreted insulin normally in response to glucose. We plan to implant these labeled beta-cells in nude rats and follow their distribution and mass by MRI. This part of work may provide us a non-invasive imaging method for future studies of transplanted islets or insulin secreted beta-cells in encapsulated devices for treating type I diabetes. We will also develop new strategies for imaging endogenous beta-cells of pancreas in transgenic mice with a diabetic genetic background. Islets and beta-cells of these mice undergo hyperplasia. The increased islet number/size will be advantageous for MRI detection. We will explore new methods for the selective labeling of beta-cells of pancreas, including selectively expressing molecular markers on beta-cells of transgenic mice, and applying beta novel class of beta-cell specific peptides isolated by the phage display technique at UTSW. This part of work may provide us MR imaging methods for studying beta-cells in diabetic animal models, and may become a powerful research tool for characterizing beta-cells in many other transgenic mice available. Future development and application of these imaging methods may help us better understand the dynamic changes of beta-cell mass and function of pancreas during the pathogenesis of type II diabetes, and may help us monitor the effects of medical treatments on beta-cells.
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