IL-7 and Lymphocyte Homeostasis: Life versus Death

IL-7 和淋巴细胞稳态：生与死

• 批准号: 7473259
• 负责人: Annette R Khaled
• 金额: $ 19.58万
• 依托单位: UNIVERSITY OF CENTRAL FLORIDA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-01 至 2010-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7473259
• 关键词: Abnormal Cell; Adult; Apoptosis; Apoptotic; Autophagocytosis; BAD gene; BAX gene; BCL-2 Protein; BCL2L11 gene; BIM Bcl-2-binding protein; Bad protein; Bax protein; Binding; Biological; Biological Assay; Cell Cycle; Cell Cycle Progression; Cell Cycle Regulation; Cell Death; Cell Line; Cell division; Cells; Cessation of life; Commit; Cyclin-Dependent Kinases; DNA biosynthesis; DNA chemical synthesis; Development; Down-Regulation; Environment; Equilibrium; Family; Family member; Future; Glucose; Glucose Transporter; Growth; Homeostasis; Immune system; Interleukin 7 Receptor; Interleukin-7; Life; Life Cycle Stages; Lymphocyte; Lymphocyte Subset; Lymphoma; Lymphomagenesis; Lymphoproliferative Disorders; MAP Kinase Gene; MAPK14 gene; Maintenance; Malignant Neoplasms; Mediating; Mediator of activation protein; Metabolic; Metabolism; Mitochondria; Modeling; Mus; Neonatal; Nutrient; Peripheral; Phase; Phosphoric Monoester Hydrolases; Phosphorylation; Physiological; Population Sizes; Process; Proteins; Purpose; Regulation; Research; Research Personnel; Resources; Role; S Phase; SLC2A1 gene; Signal Transduction; T-Lymphocyte; Testing; Tissues; Withdrawal; carcinogenesis; cell growth; cytokine; deprivation; design; glucose metabolism; glucose uptake; innovation; leukemia/lymphoma; prevent; pro-apoptotic protein; programs; research study; response; uptake

DESCRIPTION (provided by applicant): Homeostasis of the immune system is maintained through a balance of pro-life and pro-death signals, with availability of the cytokine, interleukin-7 (IL-7), a critical resource limiting population size. Cell death is a necessary process that eliminates abnormal cells in healthy tissue. Cell growth is mediated by regulation of the cell life cycle and metabolism. By exploring these biological activities of IL-7, this proposal expands the understanding of the origins of cancer. Key findings from the proposed studies will be developed into an innovative research program designed to study the role of IL-7 in lymphomagenesis. The hypothesis to be tested is that IL-7 promotes life by repressing apoptotic proteins of the BCL-2 family, while regulating cell cycling through the phosphatase, Cdc25A, and maintaining metabolic resources through glucose uptake. Loss of IL-7 triggers the apoptotic protein, BAX, which is inhibited by BCL-2. Studies suggest that the apoptotic protein, BIM, could be a target of IL-7 signaling and modulate the effector activities of BAX and BCL-2. This will be determined by examining the activity of BIM in lymphocytes - how IL-7 regulates BIM and how BIM interacts with other BCL-2 family members. The activity of IL-7 as a proliferative factor will be studied by examining the regulation and function of the phosphatase, Cdc25A, a key mediator of cell cycling. To establish the homeostatic potential of Cdc25A, cells expressing an active, stable form of Cdc25A will be evaluated for growth in an IL-7 deficient environment. The survival and proliferative activities of IL-7 may be supported by maintenance of energy resources. The factors mediating glucose uptake through IL-7 signaling will be examined in cells in which apoptosis has been inhibited or cell division induced. The approaches proposed combine the use of mouse experiments that establish physiological relevance with functional assays using cell lines to examine mechanisms underlying the activities of IL-7 essential for the homeostasis of peripheral cells. Expected findings will have significant impact in field of cytokine research.

描述（由申请方提供）：免疫系统的稳态通过促生命和促死亡信号的平衡以及细胞因子白细胞介素-7（IL-7）的可用性来维持，这是一种限制种群规模的关键资源。细胞死亡是消除健康组织中异常细胞的必要过程。细胞生长是通过调节细胞生命周期和代谢来介导的。通过探索IL-7的这些生物学活性，该提案扩展了对癌症起源的理解。这些研究的主要发现将被开发成一个创新的研究项目，旨在研究IL-7在淋巴瘤发生中的作用。待检验的假设是，IL-7通过抑制BCL-2家族的凋亡蛋白来促进生命，同时通过磷酸酶Cdc 25 A调节细胞周期，并通过葡萄糖摄取来维持代谢资源。IL-7的缺失触发凋亡蛋白BAX，其被BCL-2抑制。研究表明，凋亡蛋白BIM可能是IL-7信号转导的靶点，并调节BAX和BCL-2的效应活性。这将通过检查淋巴细胞中BIM的活性-IL-7如何调节BIM以及BIM如何与其他BCL-2家族成员相互作用来确定。将通过检查磷酸酶Cdc 25 A（细胞周期的关键介质）的调节和功能来研究IL-7作为增殖因子的活性。为了建立Cdc 25 A的稳态潜力，将评估表达活性、稳定形式的Cdc 25 A的细胞在IL-7缺陷环境中的生长。IL-7的存活和增殖活性可以通过维持能量资源来支持。通过IL-7信号传导介导葡萄糖摄取的因子将在细胞凋亡已被抑制或细胞分裂被诱导的细胞中进行检查。所提出的方法联合收割机结合使用小鼠实验，其建立生理相关性与使用细胞系的功能测定，以检查外周细胞稳态所必需的IL-7活性的潜在机制。预期的发现将在细胞因子研究领域产生重大影响。