Regulatory Role of Transcription Factor Slug in Aging

转录因子 Slug 在衰老中的调节作用

• 批准号: 8309141
• 负责人: WEN-SHU WU
• 金额: $ 33.21万
• 依托单位: CHILDREN'S HOSPITAL & RES CTR AT OAKLAND
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-01 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8309141
• 关键词: Adipose tissue; Adult; Affect; Aging; Aging-Related Process; American; Animal Model; Attenuated; Behavioral Research; Binding; Binding Sites; Biological Assay; Body Weight decreased; Boxing; Bromodeoxyuridine; CDKN2A gene; Cell Aging; Cell Cycle; Cell Cycle Arrest; Cell Cycle Progression; Cell Survival; Cells; Cellular Stress; Consensus; Cyclin-Dependent Kinase Inhibitor 2A; Cyclin-Dependent Kinases; DNA biosynthesis; Data; Development; E-Box Elements; Electrophoretic Mobility Shift Assay; Embryo; Epithelial; Event; Fibroblasts; Foundations; Genetic; Genetic Transcription; Genetically Modified Animals; Goals; Growth; HMGA2 gene; Health; Hematopoietic; Hematopoietic stem cells; Human; In Vitro; Intervention; Knock-out; Kyphosis deformity of spine; Laboratories; Learning; Link; Luciferases; Mesenchymal; Methods; Mission; Modeling; Molecular; Mus; Muscle satellite cell; Oncogene Activation; Osteoporosis; Outcome; Pathway interactions; Personal Satisfaction; Phenotype; Premature aging syndrome; Process; Promoter Regions; Public Health; Regulation; Reporter; Research; Research Project Grants; Role; Series; Site; Skeletal Muscle; Stem cells; Technology; Testing; Therapeutic; Therapeutic Intervention; Tissues; United States National Institutes of Health; Work; Zinc Fingers; adult stem cell; anti aging; chromatin immunoprecipitation; combat; derepression; improved; in vivo; inhibitor/antagonist; innovation; insight; method development; novel; overexpression; oxidative damage; p19ARF; prevent; promoter; regenerative; research study; self-renewal; senescence; slug; small hairpin RNA; social; stem; tissue regeneration; transcription factor

DESCRIPTION (provided by applicant): Recent evidence suggests that the cellular senescence machinery and the decline of the regenerative capacity of certain self-renewing stem cell compartments may contribute importantly to mammalian aging. Although derepression of INK4A/ ARF locus is thought to be an intrinsically linked event, very little is known about the specific mechanisms responsible for modulation of p16INK4 and p19ARF expression. Preliminary work from the PI's laboratory suggests that Slug, a zinc-finger transcription factor known to affect cell survival and the epithelial-mesenchymal transition in a variety of tissues, directly inhibits p16INK4 transcription, to the extent that Slug deficiency leads to cellular senescence and premature aging in vitro and in animal models. We therefore hypothesize that Slug influences aging by restraining cellular senescence and sustaining the regenerative potential of adult stem and progenitor cells, primarily through direct negative regulation of the p16INK4 gene. These developments promote our long-term objective -- to discover novel molecular pathways underlying the senescence of both differentiated and stem and progenitor cells -- and have led to three immediate research aims to determine the precise contribution of Slug to organismal aging. Aim 1 will establish the extent to which p16INK4a contributes to accelerated senescence in Slug-deficient MEFs using both knockdown and knockout technologies. Aim 2 will attempt to elucidate the molecular mechanisms by which Slug negatively regulates expression of p16INK4a, by relying on chromatin immunoprecipitation and electrophoretic mobility shift assays. Aim 3 will define the functional role of Slug in tissue senescence and the regenerative potential of adult stem and progenitor cells. These experiments will use a series of genetically modified animal models as well as hematopoietic and skeletal muscle stem cells from Slug and p16INK4a- deficient mice. This proposal is innovative because it exploits a transcription factor, Slug, with unique regulatory activity at the INK4a/ ARF locus. The likelihood that a better understanding of the in vivo regulation of this locus, and hence of mammalian aging, will emerge from our project appears high.

描述（由申请人提供）：最近的证据表明，细胞衰老机制和某些自我更新干细胞区室再生能力的下降可能对哺乳动物衰老有重要作用。尽管INK 4A/ ARF基因座的去抑制被认为是一个内在联系的事件，但对p16 INK 4和p19 ARF表达调节的具体机制知之甚少。PI实验室的初步工作表明，Slug是一种锌指转录因子，已知会影响各种组织中的细胞存活和上皮-间充质转化，直接抑制p16 INK 4转录，以至于Slug缺乏会导致体外和动物模型中的细胞衰老和过早衰老。因此，我们假设鼻涕虫通过抑制细胞衰老和维持成体干细胞和祖细胞的再生潜力来影响衰老，主要是通过p16 INK 4基因的直接负调控。这些发展促进了我们的长期目标-发现分化细胞、干细胞和祖细胞衰老的新分子途径-并导致了三个直接的研究目标，以确定鼻涕虫对生物体衰老的精确贡献。目的1将建立在何种程度上p16 INK 4a有助于在蛞蝓缺陷MEFs使用敲除和敲除技术加速衰老。目的2将试图阐明Slug负调控p16 INK 4a表达的分子机制，依赖于染色质免疫沉淀和电泳迁移率变动分析。目的3将明确Slug在组织衰老中的功能作用以及成体干细胞和祖细胞的再生潜力。这些实验将使用一系列转基因动物模型以及来自Slug和p16 INK 4a缺陷小鼠的造血和骨骼肌干细胞。这个提议是创新的，因为它利用了一种转录因子Slug，在INK 4a/ ARF位点具有独特的调节活性。更好地了解该基因座的体内调控，从而了解哺乳动物衰老的可能性，将从我们的项目中出现。