Bioengineering A Bioartificial Pancreas

生物工程生物人工胰腺

• 批准号: 7655762
• 负责人: Emmanuel C. Opara
• 金额: $ 50.88万
• 依托单位: WAKE FOREST UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-05 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7655762
• 关键词: Acids; Address; Alginates; Allografting; Angiogenic Proteins; Animal Model; Animals; Biomedical Engineering; Blood Circulation; Blood Glucose; Blood capillaries; Blood flow; C-Peptide; Caliber; Cells; Chimera organism; Clinical; Control Animal; Control Groups; Data; Diffusion; Drug Formulations; Encapsulated; Endocrine; Evaluation; Exclusion; Experimental Models; Fibroblast Growth Factor 1; Gel; Glucocorticoids; Glucose; Graft Rejection; Greater sac of peritoneum; Growth Factor; Human; Imaging Techniques; Immunosuppression; Immunosuppressive Agents; In Vitro; Inbred Lew Rats; Inbred WF Rats; Individual; Insulin; Insulin-Dependent Diabetes Mellitus; Islets of Langerhans Transplantation; Isogenic transplantation; Kinetics; Length; Liver; Longevity; Measurement; Measures; Metabolism; Methods; Microcapsules drug delivery system; Microencapsulations; Modeling; Monkeys; Nature; Nutrient; Nutritional; Omentum; Outcome; Oxygen; Oxygen measurement, partial pressure, arterial; Pancreas; Patients; Permeability; Pharmaceutical Preparations; Principal Investigator; Problem Solving; Procedures; Proteins; Protocols documentation; Rattus; Reaction; Reporting; Resected; Resistance; Retrieval; Site; Source; Starvation; Steroids; Streptozocin; Structure; Surface; System; Techniques; Testing; Therapeutic; Three-Dimensional Imaging; Thrombin; Tissues; Toxic effect; Transplant Recipients; Transplantation; Treatment Protocols; Vascular blood supply; Vascularization; Viscosity; Waste Products; Work; Xenograft procedure; angiogen; base; capillary; cohort; density; design; diabetic; diabetic patient; diabetic rat; fluorescence imaging; follow-up; graft failure; image processing; improved; improved functioning; in vitro Model; in vitro testing; in vivo; islet; islet xenograft; method development; mutant; neovascularization; novel; pleiotrophin; polyornithine; prevent; programs; public health relevance; research study; response; theories

DESCRIPTION (provided by applicant): Despite the promise of the Edmonton protocol, the need to use immunosuppressive drugs and the severe shortage of human islets remain major barriers to clinical islet transplantation. An attractive strategy to overcome these two barriers is the technique of microencapsulation of islets prior to transplantation. Still, there are a number of issues that need to be resolved before this approach can become a clinical reality. Microencapsulated islet transplantation is currently performed in the unmodified peritoneal cavity because of the need for a large space to accommodate the large graft volume for which conventional islet transplant sites, such as the liver, are not suitable. The relatively large surface-to-volume ratio of microcapsules and the absence of a blood supply in the peritoneal cavity pose challenges to adequate supply of oxygen and nutrients to the encapsulated islets as well as exchange of glucose and insulin between the encapsulated islets and the systemic circulation. We will test the hypothesis that neovascularization of encapsulated islet transplants would enhance the viability of the islets because of adequate supply of oxygen and nutrients. The specific aims of this proposal are: 1) To design an optimum delivery system for angiogenic proteins to induce neovascularization around alginate microcapsules. After encapsulating the novel HBGAM-R136K angiogen in either of the alginate layers of alginate-polyornithine- alginate microcapsules, we will first study its release kinetics in vitro and the nature and level of microvasculature in vitro using fluorescence and image processing techniques. We will then examine tissue angiogenic and fibrotic responses to the protein in in vivo studies. 2) To determine the function of islets encapsulated and transplanted with the angiogenic protein to induce neovascularization. Using an isograft model of normal Lewis rat islet donors and Streptozotocin-diabetic Lewis rat recipients, we will co- encapsulate islets with angiogenic protein, and will assess blood glucose and insulin levels for 90 days after transplantation in omentum pouches of recipients. 3) To determine the efficacy of the optimized model of this bioartificial pancreas in a rat allograft. We will isolate and encapsulate islets from normal Wistar-Furth rats and transplant them in diabetic Lewis rats. 4) To assess the bioartificial pancreas function in xenograft animal models - first, human islets transplanted in diabetic Lewis rats for 90 days; and second, human islet transplants in diabetic monkeys for 180 days. PUBLIC HEALTH RELEVANCE: It is now clear that islet transplantation provides the best treatment option for individuals afflicted with Type 1 diabetes. However, the shortage of human islets and the need to use risky drugs to prevent transplant rejection remain major obstacles to routine use of islet transplantation in diabetic patients. The purpose of this project is to develop a viable strategy to overcome these two barriers and make islet transplantation a more appealing and widely used treatment option for diabetic patients.

描述(申请人提供)：尽管埃德蒙顿方案有希望，但需要使用免疫抑制药物和人类胰岛的严重短缺仍然是临床胰岛移植的主要障碍。克服这两个障碍的一个有吸引力的策略是在移植前对胰岛进行微囊化技术。尽管如此，在这种方法可以成为临床现实之前，仍有许多问题需要解决。微囊化胰岛移植目前在未经改良的腹膜腔内进行，因为需要一个大的空间来容纳大的移植物体积，而传统的胰岛移植部位，如肝脏，不适合于这些移植物。微囊相对较大的表面积与体积比以及腹膜腔内缺乏血液供应，对被包裹的胰岛的足够氧气和营养供应以及被包裹的胰岛与体循环之间的葡萄糖和胰岛素交换构成了挑战。我们将验证这样的假设，即包膜胰岛移植的新生血管可以提高胰岛的生存能力，因为有足够的氧气和营养供应。这项建议的具体目的是：1)设计一种最佳的血管生成蛋白递送系统，以诱导藻酸盐微胶囊周围的新生血管形成。将新型HBGAM-R136K微囊包裹在海藻酸盐-聚鸟氨酸-海藻酸盐微囊的海藻酸层中后，我们将首先利用荧光和图像处理技术研究其体外释放动力学和体外微血管形成的性质和水平。然后，我们将在活体研究中检查组织对该蛋白的血管生成和纤维化反应。2)检测包裹血管生成蛋白的胰岛在诱导新生血管中的作用。使用正常的Lewis大鼠胰岛供体和链脲佐菌素-糖尿病Lewis大鼠受体的同种异体移植模型，我们将用血管生成蛋白共包裹胰岛，并在受体的大网膜袋中评估移植后90天的血糖和胰岛素水平。3)确定优化的生物人工胰腺模型在大鼠同种异体移植中的效果。我们将分离和包裹正常Wistar-Furth大鼠的胰岛，并将它们移植到糖尿病Lewis大鼠体内。4)评估异种移植动物模型中的生物人工胰腺功能--第一，人胰岛移植到糖尿病Lewis大鼠体内90天；第二，人胰岛移植到糖尿病猴体内180天。公共卫生相关性：现在很明显，胰岛移植为患有1型糖尿病的患者提供了最佳的治疗选择。然而，人类胰岛的短缺和需要使用高风险的药物来防止移植排斥反应仍然是糖尿病患者常规使用胰岛移植的主要障碍。这个项目的目的是开发一种可行的策略来克服这两个障碍，使胰岛移植成为对糖尿病患者更有吸引力和更广泛使用的治疗选择。