IL-7 and Lymphocyte Homeostasis: Life versus Death

免疫系统的稳态通过亲生命和亲死亡信号的平衡来维持， 细胞因子白细胞介素-7（IL-7）的可用性，这是限制人口规模的关键资源。细胞死亡是一种 这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 细胞的生命周期和新陈代谢。通过探索IL-7的这些生物学活性，该提议扩展了IL-7的生物学活性。 了解癌症的起源。拟议研究的主要结果将发展成为一个 创新的研究计划，旨在研究IL-7在淋巴瘤发生中的作用。假设是 IL-7通过抑制BCL-2家族的凋亡蛋白来促进生命，同时调节细胞凋亡。 通过磷酸酶Cdc 25 A循环，并通过葡萄糖摄取维持代谢资源。 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这将通过检查淋巴细胞中BIM的活性来确定-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。IL-7作为增殖因子的活性将是 通过检测磷酸酶Cdc 25 A的调节和功能来研究，Cdc 25 A是细胞周期的关键介质。 为了建立Cdc 25 A的体内平衡潜力，将表达活性、稳定形式的Cdc 25 A的细胞在体外培养。 评估在IL-7缺乏环境中的生长。IL-7的存活和增殖活性可能是 以维持能源资源为支撑。通过IL-7介导葡萄糖摄取的因素 将在细胞凋亡已被抑制或细胞分裂已被诱导的细胞中检测信号传导。的 所提出的方法联合收割机结合使用小鼠实验， 使用细胞系的功能测定，以检查IL-7活性的基础机制， 外周细胞的稳态。预期的发现将在细胞因子研究领域产生重大影响。

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.