alpha-Endosulfine, Insulin,& Adult Tissue Growth Control

α-硫磺、胰岛素、

• 批准号: 7065358
• 负责人: Daniela Drummond-Barbosa
• 金额: $ 5.13万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-05-01 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7065358
• 关键词: alpha; Endosulfine; Insulin; Adult; Tissue

DESCRIPTION (provided by applicant): Little is known about how adult tissues maintained by stem cells sense and respond to external stimuli such as changes in nutrition. We established the Drosophila ovary as a model system in which to study this question. We showed that nutritional status can control the number of cells produced in the Drosophila ovary, and that the insulin pathway and (z-endosulfine are part of the regulatory machinery. In mammals, a-endosulfine is likely to be involved in the regulation of ion channels and in the secretion of insulin; however, the available evidence as to its precise role is conflicting. In pancreatic ¿ cells in culture, a-endosulfine binds to the regulatory subunit, SUR, of a potassium channel, triggering membrane depolarization, calcium influx and secretion of insulin. In other studies, a-endosulfine was shown to inhibit insulin secretion by blocking calcium channels. Genetic analyses, which will be crucial in resolving the current controversies and understanding the in vivo role of a-endosulfine, have not yet been conducted. We propose a focused set of genetic approaches, combined with biochemical and cell biological assays, to address the role of a-endosulfine in tissue growth regulation, and test the hypothesis that it regulates ion channel activityand insulin secretion in vivo. The specific aims are: (1) to determine in what tissue a-endosulfine is required and if it is involved in insulin secretion; (2) to determine if a-endosulfine acts via the modulation SUR activity; and (3) to carry out structure-function analysis of a-endosulfine. These approaches will contribute significantly to the understanding of the role of a-endosulfine in insulin secretion, as well as of normal biological processes in which insulin is required. In particular, they will help elucidate mechanisms that lead to type II diabetes, an important step towards the development of new drugs to treat this disease. In addition, these studies will provide new insights into how stem cell-supported tissues respond to nutritional changes and, perhaps, identify new ways to manipulate this response for therapeutic purposes.

描述（由申请人提供）：关于干细胞维持的成体组织如何感知和响应外部刺激（如营养变化），我们知之甚少。我们建立了果蝇卵巢作为研究这个问题的模型系统。我们发现，营养状况可以控制果蝇卵巢中产生的细胞数量，胰岛素途径和β-内硫素是调节机制的一部分。在哺乳动物中，α-硫丹可能参与离子通道的调节和胰岛素的分泌;然而，关于其确切作用的现有证据相互矛盾。在胰腺中，在培养的细胞中，α-内硫素与钾通道的调节亚基SUR结合，触发膜去极化、钙内流和胰岛素分泌。在其他的研究中，α-内砜被证明通过阻断钙通道来抑制胰岛素分泌。遗传分析对于解决目前的争议和了解α-硫丹的体内作用至关重要，但尚未进行。我们提出了一套集中的遗传学方法，结合生物化学和细胞生物学测定，以解决α-硫丹在组织生长调节中的作用，并测试它在体内调节离子通道活性和胰岛素分泌的假设。具体目标是：（1）确定在什么组织中需要α-内砜以及它是否参与胰岛素分泌;（2）确定α-内砜是否通过调节SUR活性起作用;和（3）进行α-内砜的结构-功能分析。这些方法将大大有助于了解α-内砜在胰岛素分泌中的作用，以及胰岛素所需的正常生物过程。特别是，它们将有助于阐明导致II型糖尿病的机制，这是开发治疗这种疾病的新药的重要一步。此外，这些研究将为干细胞支持的组织如何应对营养变化提供新的见解，并可能确定新的方法来操纵这种反应用于治疗目的。