Regulation of mesodermal progenitors in transgenic zebrafish

转基因斑马鱼中胚层祖细胞的调控

• 批准号: 7631225
• 负责人: David Kimelman
• 金额: $ 32.34万
• 依托单位: UNIVERSITY OF WASHINGTON
• 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 2012-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7631225
• 关键词: Anterior; Binding; Biological Models; Boxing; Brachyury protein; Cell Maintenance; Cell Transplantation; Cell Transplants; Cells; Commit; Defect; Development; Disease; Down-Regulation; Embryo; Environment; Gastrula; Gene Expression; Genes; Genetic Transcription; Heat-Shock Response; Injection of therapeutic agent; Knock-out; Label; Left; Life; Mammals; Mesoderm Cell; Messenger RNA; Methods; Modeling; Orthologous Gene; Pattern; Play; Population; Process; Regulation; Reporter; Resources; Rest; Role; Signal Transduction; Somites; Staging; Stem cells; System; Tail; Technology; Testing; Time; Tissues; Transgenic Organisms; Up-Regulation; Vertebrates; Work; Zebrafish; blastomere structure; cell behavior; in vivo; mutant; novel strategies; progenitor; somitogenesis; transcription factor

DESCRIPTION (provided by applicant): A large body of evidence in vertebrates shows that the development of the anterior trunk and the rest of the body are differentially regulated. Previous studies using mutants, knockouts, morpholinos and mRNA injection have provided very important information on the role of signaling and transcription factors in establishing the embryonic vertebrate body plan during the early gastrula stages. However, because alterations in the patterning of the early gastrula embryo cause such severe embryological defects, it has been difficult to study later stages when most of the body develops. Using transgenic lines containing heat-shock inducible cell autonomous regulators of signaling and transcription, together with a new transgenic line we developed that allows us to temporally and specifically label the mesodermal progenitors, we now have the ability to determine how the mesodermal progenitors are regulated by signaling and T-box transcription factors to progressively differentiate during somitogenesis, a process that is essential for forming a normal body and is conserved in all vertebrates. The studies described here take advantage of the ability in zebrafish to analyze the mesodermal progenitors at the single-cell level in living embryos, using cell transplants to study experimentally cell-autonomously perturbed cells within a normal background. This novel approach will allow us to examine cell behaviors that are obscured when all of the embryonic cells have alterations in signaling or transcription. Studies, particularly in mammals, show that the mesodermal progenitors are a stem-cell like population, which normally has a defined lifetime. With recent advances in the technology to produce transgenic lines, combined with the ability to study progenitors in living embryos using fluorescent reporters, zebrafish provides an excellent model system for understanding how vertebrate stem cells are regulated in vivo. As stem cells have great promise for the treatment of many diseases, the studies described here will provide valuable information about the signaling networks and transcription factors that control stem cell maintenance and tissue formation. Studies, particularly in mammals, show that the mesodermal progenitors are a stem-cell like population, which normally has a defined lifetime. With recent advances in the technology to produce transgenic lines, combined with the ability to study progenitors in living embryos using fluorescent reporters, zebrafish provides an excellent model system for understanding how vertebrate stem cells are regulated in vivo. As stem cells have great promise for the treatment of many diseases, the studies described here will provide valuable information about the signaling networks and transcription factors that control stem cell maintenance and tissue formation.

描述（由申请人提供）： 脊椎动物中的大量证据表明，前躯干和身体其他部分的发育受到不同的调节。以前的研究使用突变体，敲除，吗啉和mRNA注射提供了非常重要的信息，在早期原肠胚阶段的信号和转录因子在建立胚胎脊椎动物的身体计划的作用。然而，由于早期原肠胚胚胎模式的改变会导致如此严重的胚胎学缺陷，因此很难研究身体大部分发育的后期阶段。使用含有热休克诱导的细胞信号传导和转录自主调节因子的转基因系，以及我们开发的允许我们暂时和特异性标记中胚层祖细胞的新转基因系，我们现在有能力确定中胚层祖细胞如何受信号传导和T-box转录因子的调节，以在体节发生期间逐步分化，形成正常身体所必需的过程，在所有脊椎动物中都存在。这里描述的研究利用斑马鱼在活胚胎中的单细胞水平上分析中胚层祖细胞的能力，使用细胞移植来研究正常背景下实验性细胞自主扰动的细胞。这种新方法将使我们能够检查当所有胚胎细胞在信号或转录方面发生变化时被掩盖的细胞行为。特别是在哺乳动物中的研究表明，中胚层祖细胞是干细胞样群体，其通常具有确定的寿命。随着转基因品系生产技术的最新进展，以及使用荧光报告基因研究活胚胎中祖细胞的能力，斑马鱼为了解脊椎动物干细胞在体内的调控提供了一个很好的模型系统。由于干细胞在治疗许多疾病方面具有巨大的前景，本文所述的研究将提供有关控制干细胞维持和组织形成的信号网络和转录因子的有价值的信息。特别是在哺乳动物中的研究表明，中胚层祖细胞是干细胞样群体，其通常具有确定的寿命。随着转基因品系生产技术的最新进展，以及使用荧光报告基因研究活胚胎中祖细胞的能力，斑马鱼为了解脊椎动物干细胞在体内的调控提供了一个很好的模型系统。由于干细胞在治疗许多疾病方面具有巨大的前景，本文所述的研究将提供有关控制干细胞维持和组织形成的信号网络和转录因子的有价值的信息。