Defining the mechanisms of secretion in the Drosophila salivary gland

定义果蝇唾液腺的分泌机制

• 批准号: 7880078
• 负责人: Rebecca Marie Fox
• 金额: $ 5.3万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7880078
• 关键词: Address; Alleles; Antibodies; B-Lymphocytes; Binding; Binding Sites; Bioinformatics; Biological Assay; Biological Models; Blood Glucose; CREB1 gene; Cells; Confocal Microscopy; Consensus; Defect; Development; Diabetes Mellitus; Digestion; Disease; Drosophila genome; Drosophila genus; Electrophoretic Mobility Shift Assay; Embryo; Enhancers; Enzymes; Exhibits; Food; Foundations; Foxes; Functional disorder; Gene Components; Gene Expression; Gene Targeting; Genes; Genetic; Glucagon; Goals; Hematopoietic Neoplasms; Homologous Gene; Hormones; Human; Immune system; In Situ Hybridization; In Vitro; Infection; Insulin; Knock-out; Learning; Libraries; Mediating; Metabolism; Methods; Multiple Myeloma; Mutate; Mutation; Normal Cell; Organ; Organelles; Organism; Pancreas; Pancreatitis; Pathogenesis; Pathway interactions; Phosphorus; Plasma Cells; Play; Proteins; Regulation; Reporter Genes; Role; Salivary Glands; Site; System; Transmission Electron Microscopy; Up-Regulation; Work; biological adaptation to stress; blood glucose regulation; differentiated B cell; fighting; fly; homologous recombination; human disease; in vivo; interest; loss of function; mutant; plasma cell differentiation; research study; response; therapeutic development; transcription factor

DESCRIPTION (provided by applicant): Many specialized organs require high-level secretory activity to perform their normal functions. For example, in the immune system, B-cells differentiate into plasma cells by up-regulating the secretory machinery, thereby acquiring the ability to secrete large amounts of antibodies that fight infection and disease. Also, the pancreas secretes digestive enzymes that aid in food metabolism, as well as hormones that regulate blood glucose levels (i.e. glucagons and insulin). Correspondingly, loss of secretory control has been attributed to the pathogenesis of many human diseases, including pancreatitis and diabetes, as well as the blood cancer, multiple myeloma. One key to understanding secretory organ development and function is to define the mechanisms whereby normal cells gain the ability to secrete large amounts of protein. To do this, I will use a model system, the Drosophila salivary gland, which is the largest secretory organ in this organism and consists of cells that are specialized for high-level secretion. Two salivary gland expressed transcription factors (proteins that regulate expression of other genes) CrebA and Xbp1, have a role in regulating secretory activity. CrebA is required for the high level expression of 34 known secretory pathway component genes in the salivary gland. Consistent with this finding, CrebA mutants exhibit defects in secretory function. Xbp1 is a highly conserved transcription factor involved in ER stress response and whose mammalian counterpart is normally required for B-cells to become antibody secreting plasma cells. In Drosophila, Xbp1 is highly expressed in the embryonic salivary gland. Thus, I propose that CrebA and Xbp1 may function cooperatively to initiate and maintain the high-level secretory function of this organ. My studies will determine if CrebA and Xbp1 work in the same or parallel pathways to mediate secretory activity, if CrebA and xbpl mutants have defects in the secretory machinery, and if CrebA and/or Xbp1 directly regulate expression of the genes required to make this machinery. Finally, I will identify all of the genes that depend on CrebA and Xbp1 for their expression in the salivary gland, potentially revealing additional factors necessary for secretory function. Since both CrebA and Xbp1 homologues exist in humans, the mechanisms required to regulate secretory activity in the Drosophila salivary gland are likely to be conserved. Thus, these studies will provide a foundation for the development of therapeutics to treat diseases characterized by secretory dysfunction.

描述（由申请人提供）：许多专门的器官需要高水平的分泌活动来执行其正常功能。例如，在免疫系统中，B细胞通过上调分泌机制分化为浆细胞，从而获得分泌大量抗体的能力，这些抗体可以对抗感染和疾病。此外，胰腺分泌有助于食物代谢的消化酶，以及调节血糖水平的激素（即胰高血糖素和胰岛素）。相应地，分泌控制的丧失已被归因于许多人类疾病的发病机制，包括胰腺炎和糖尿病，以及血癌、多发性骨髓瘤。理解分泌器官发育和功能的一个关键是确定正常细胞获得分泌大量蛋白质的能力的机制。为了做到这一点，我将使用一个模型系统，果蝇唾液腺，它是这种生物体中最大的分泌器官，由专门用于高水平分泌的细胞组成。 两种唾液腺表达的转录因子（调节其他基因表达的蛋白质）CrebA和Xbp 1在调节分泌活性中起作用。CrebA是唾液腺中34种已知分泌途径组分基因高水平表达所必需的。与这一发现相一致，CrebA突变体表现出分泌功能的缺陷。Xbp 1是一种参与ER应激反应的高度保守的转录因子，其哺乳动物对应物通常是B细胞成为分泌抗体的浆细胞所需的。在果蝇中，Xbp 1在胚胎唾液腺中高度表达。因此，我建议，CrebA和Xbp 1可能发挥作用，合作启动和维持高水平的分泌功能，这一器官。我的研究将确定CrebA和Xbp 1是否以相同或平行的途径介导分泌活性，CrebA和Xbp 1突变体是否在分泌机制中存在缺陷，以及CrebA和/或Xbp 1是否直接调节制造这种机制所需的基因表达。最后，我将确定所有依赖于CrebA和Xbp 1在唾液腺中表达的基因，可能揭示分泌功能所需的其他因素。由于CrebA和Xbp 1同源物都存在于人类中，因此调节果蝇唾液腺分泌活性所需的机制可能是保守的。因此，这些研究将为开发治疗以分泌功能障碍为特征的疾病的疗法提供基础。