Aging and thymopoiesis: Changes in stroma, T-presursors

衰老和胸腺生成：基质、T 前体的变化

• 批准号: 7273629
• 负责人: PHONG T LE
• 金额: $ 26.6万
• 依托单位: LOYOLA UNIVERSITY CHICAGO
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-08-15 至 2009-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7273629
• 关键词: Address; Affect; Age; Aging; Antigens; Autoimmune Diseases; Bone Marrow Transplantation; CD44 gene; CD8B1 gene; Cell Aging; Cell Count; Cell physiology; Cells; Cellularity; Chronically Ill; Commit; Complex; Condition; DNA Sequence Rearrangement; Data; Development; Disease; Elderly; Epithelial; Epithelium; Essential Genes; Event; Gene Targeting; Genetic Transcription; Goals; HIV; Human; IL2RA gene; Immune response; Immunologic Deficiency Syndromes; Incidence; Infection; Knowledge; Lead; Life; Ligands; Lymphoid; Mature T-Lymphocyte; Molecular; Mus; Numbers; Organ; Organogenesis; Output; Pathway interactions; Patients; Peripheral; Process; Production; Protein Overexpression; Research; Research Personnel; Rodent; Signal Transduction; Staging; Stem cells; T-Cell Development; T-Cell Receptor; T-Lymphocyte; Thymic epithelial cell; Thymocyte Development; Thymus Gland; Transgenic Mice; aged; alpha-beta T-Cell Receptor; base; cell age; cell growth; chemotherapy; member; molecular array; notch protein; novel strategies; progenitor; programs; receptor; thymocyte; tool; transcription factor

DESCRIPTION (provided by applicant): The thymus has crucial functions in the development of most naive T cells for the peripheral naive T cell pool in humans and rodents. Despite this essential function, the thymus involutes with age, leading to a dramatic reduction in naive T cell output. Thus, aging is associated with increased incidence of potentially life-threatening infections and autoimmune diseases. Our recent findings and the proposed studies indicate that it might be possible to ameliorate such reduced thymopoiesis. To do so, we must first understand the cellular and molecular changes that lead to thymic involution, which is the long-term goal of our research. Clinically, this knowledge will help us develop novel strategies to rejuvenate the thymus and increase thymic output of naive T cells in the elderly or chronically ill, in patients with immunodeficiency diseases such as HIV, and in patients undergoing chemotherapy or bone marrow transplant. The development of T cells or thymocytes in the thymus depends on thymic epithelial stroma and is regulated by transcription factors whose temporal expression is tightly regulated. We hypothesize that Notch signaling is at the apex of the signal cascade that orchestrates the coordinated expression of transcription factors critical for T lineage commitment and differentiation as well as thymic epithelial cell functional maturation. Changes in the temporal expression of transcription factors that control the development of the immature triple negative (TN) thymocytes result in lower thymic naive T cell output. We also hypothesize that thymic epithelial stroma modulates changes in the expression of these transcription factors. The development of TN thymocytes requires T lineage commitment, cell expansion, and rearrangement of T cell receptors beta and alpha. We propose four specific aims: Aim 1, to determine whether T cell commitment is altered in the aged thymus; Aim 2, to determine whether cell expansion is altered during DN thymocyte development; Aim 3, to determine whether rearrangement of T cell receptors beta and alpha are altered in DN development in the aged thymus; Aim 4, to determine how Notch signaling regulates FoxN1 transcription. We have generated transgenic mice for the epithelium-specific transcription factor Foxn1. These mice show absence of age- associated changes in DN development and are a unique tool for delineating the control of expression of transcription factors in aged thymocytes and the function of thymic epithelial stroma in this process.

描述（由申请方提供）：胸腺在人类和啮齿类动物外周幼稚T细胞池的大多数幼稚T细胞发育中具有关键作用。尽管有这一基本功能，胸腺随着年龄的增长而退化，导致幼稚T细胞输出急剧减少。因此，衰老与潜在危及生命的感染和自身免疫性疾病的发病率增加有关。我们最近的发现和拟议的研究表明，这可能是可能的，以改善这种减少胸腺细胞。为此，我们必须首先了解导致胸腺退化的细胞和分子变化，这是我们研究的长期目标。在临床上，这些知识将帮助我们开发新的策略，以恢复胸腺和增加胸腺输出的幼稚T细胞在老年人或慢性病患者，免疫缺陷疾病，如艾滋病毒，并在接受化疗或骨髓移植的患者。胸腺中T细胞或胸腺细胞的发育依赖于胸腺上皮基质，并受转录因子的调节，转录因子的时间表达受到严格调节。我们假设Notch信号传导处于信号级联的顶点，该信号级联协调对T谱系定型和分化以及胸腺上皮细胞功能成熟至关重要的转录因子的协调表达。控制未成熟三阴性（TN）胸腺细胞发育的转录因子的时间表达的变化导致胸腺幼稚T细胞输出降低。我们还假设胸腺上皮基质调节这些转录因子表达的变化。TN胸腺细胞的发育需要T谱系定型、细胞扩增和T细胞受体β和α的重排。我们提出四个具体目标：目的1，以确定是否T细胞的承诺是改变在老年胸腺;目的2，以确定是否细胞扩张是改变在DN胸腺细胞的发展;目的3，以确定是否重排的T细胞受体β和α在DN的发展在老年胸腺改变;目的4，以确定如何Notch信号调节FoxN 1转录。我们已经产生了上皮特异性转录因子Foxn 1的转基因小鼠。这些小鼠显示在DN发展中不存在与年龄相关的变化，并且是用于描绘衰老胸腺细胞中转录因子表达的控制和胸腺上皮基质在该过程中的功能的独特工具。