Islet Biology in Cystic Fibrosis Related Diabetes

囊性纤维化相关糖尿病中的胰岛生物学

• 批准号: 8447218
• 负责人: Lydia Aguilar-Bryan
• 金额: $ 60.03万
• 依托单位: PACIFIC NORTHWEST RESEARCH INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-15 至 2017-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8447218
• 关键词: 3 year old; Affect; Age-Years; Amyloid; Apoptosis; Atrophic; Biology; Caucasians; Caucasoid Race; Cell Death; Cell Proliferation; Cell physiology; Cells; Cellular biology; Chemicals; Clinic; Clinical Research; Complication; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Data; Deposition; Development; Diabetes Mellitus; Diagnosis; Diet; Electrophysiology (science); Exocrine pancreas; Exocrine pancreatic insufficiency; Exocytosis; Exposure to; Fatty acid glycerol esters; Fibrosis; Functional disorder; Gene Expression; Glucagon; Glucose Intolerance; Health; Hereditary Disease; Human; Hyperglycemia; In Vitro; Individual; Inflammation; Insulin; Insulin Resistance; Intestines; Ion Channel; Islet Cell; Islets of Langerhans; Knock-out; Lead; Leptin receptor mutation; Life; Longevity; Lung; Metabolic; Molecular; Morphology; Mus; Mutation; Nutritional; Oxidative Stress; Pancreas; Pancreatitis; Pathogenesis; Patients; Play; Proteins; Quality of life; Risk; Role; Sampling; Signal Transduction; Stress; Testing; cystic fibrosis patients; cytokine; improved; in vivo; insulin secretion; islet; mouse model; multidisciplinary; mutant; protein transport; response; stressor

DESCRIPTION (provided by applicant): Cystic fibrosis-related diabetes (CFRD) is commonly thought to be a consequence of insulin deficiency combined with insulin resistance. However, this explanation is not satisfactory because clinical studies in CFRD show inadequate insulin secretion but little evidence for insulin resistance. Furthermore, the commonly accepted pathogenesis for the insulin deficiency, namely that the pancreatitis of cystic fibrosis (CF) and subsequent pancreatic atrophy and fibrosis lead to islet destruction, is not likely a sufficient explanation. Since the cystic fibrosis transmembrane conductance regulator (CFTR) is expressed and functional in mouse and human pancreatic islet cells, we propose that CFTR mutations directly impair islet cell function and health. In this proposal, we will test the hypotheses that CFTR plays an important regulatory role in insulin and glucagon secretion and that mutations in CFTR lead to ¿ cell dysfunction, inadequate ¿ cell adaptation to islet "stressors" (pancreatitis, inflammation, hyperglycemia), and reduced ¿ cell mass, thus greatly increasing the risk for diabetes mellitus. We propose an integrated, multiple component pathogenesis involving abnormal CFTR ion channel activity and abnormal CFTR protein trafficking and cell biology, leading to secretory dysfunction, ¿ cell ER stress, and ¿ cell death. Our multidisciplinary team with expertise in electrophysiology, human islet biology, and CF will conduct in vitro and in vivo studies using unique mouse models and human islets to test these hypotheses and to discover information important for understanding the pathogenesis of human CFRD. We will pursue three aims: 1) Define the role of CFTR in regulating insulin and glucagon secretion and ¿ cell function and health by studying islets lacking CFTR; 2)Determine the impact of selected CF mutations on insulin and glucagon secretion and ¿ cell function and health; and 3) Determine the impact of selected CF mutations on ¿ cell function, health, and adaptation in response to "islet stressors" such as pancreatitis, hyperglycemia, and insulin resistance. PUBLIC HEALTH RELEVANCE: Cystic fibrosis (CF) is the most common hereditary disease in Caucasians. Most of the patients are diagnosed at 2-3 years of age and treatment is focused on improving survival and quality of life and recommended to take place at a cystic fibrosis clinic where the lung, bowel and nutritional problems can be properly managed. Over the last three decades, improvement in treatment has increased life span to 40-50 years of age and cystic fibrosis-related diabetes (CFRD) has become the most common complication. A better understanding of the cellular and molecular mechanisms that result in CFRD will be fundamental for the improvement of diagnosis and treatment of this severe CF complication.

描述（由申请人提供）：囊性纤维化相关性糖尿病（CFRD）通常被认为是胰岛素缺乏合并胰岛素抵抗的结果。然而，这种解释并不令人满意，因为临床研究显示CFRD的胰岛素分泌不足，但几乎没有胰岛素抵抗的证据。此外，普遍接受的胰岛素缺乏的发病机制，即囊性纤维化胰腺炎（CF）和随后的胰腺萎缩和纤维化导致胰岛破坏，不太可能是一个充分的解释。由于囊性纤维化跨膜传导调节因子（CFTR）在小鼠和人胰岛细胞中表达和发挥功能，我们提出CFTR突变直接损害胰岛细胞功能和健康。在本研究中，我们将验证CFTR在胰岛素和胰高血糖素分泌中发挥重要调节作用的假设，以及CFTR突变导致细胞功能障碍、细胞对胰岛“应激源”（胰腺炎、炎症、高血糖）适应不足和细胞质量减少，从而大大增加糖尿病风险的假设。我们提出了一个综合的、多组分的发病机制，涉及CFTR离子通道活性异常、CFTR蛋白转运异常和细胞生物学，导致分泌功能障碍、细胞内质网应激和细胞死亡。