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Wnt signaling in zebrafish fin regeneration: Chemical biology using a GSK3Beta inhibitor.

机译:斑马鱼鳍再生中的Wnt信号传导:使用GSK3Beta抑制剂的化学生物学。

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摘要

Bone growth can be impaired due to disease, such as osteoporosis. Currently, intermittent parathyroid hormone (PTH) treatment is the only approved therapy in the United States for anabolic bone growth in osteoporosis patients. The anabolic effects of PTH treatment are due, at least in part, to modulation of the Wnt/beta-catenin pathway. Activation of the Wnt/beta-catenin pathway using a small molecule inhibitor of GSK3beta was previously shown to increase markers of bone formation in vitro. Our study utilized a zebrafish model system to study Wnt activated fin regeneration and bone growth. Wnt signaling is the first genetically identified step in fin regeneration, and bony rays are the main structure in zebrafish fins. Thus, zebrafish fin regeneration may be a useful model to study Wnt signaling mediated bone growth. Fin regeneration experiments were conducted using various concentrations of a GSK3beta inhibitor compound, LSN 2105786, for different treatment periods and regenerative outgrowth was measured at 4 and 7 days post amputation. Experiments revealed continuous low concentration (4-5 nM) treatment to be most effective at increasing regeneration. Higher concentrations inhibited fin growth, perhaps by excessive stimulation of differentiation programs. In situ hybridization experiments were performed to examine effects of GSK3beta inhibitor on Wnt responsive gene expression. Experiments showed temporal and spatial changes on individual gene markers following GSK3beta inhibitor treatment. Additionally, confocal microscopy and immunofluorescence labeling data indicated that the Wnt signaling intracellular signal transducer, beta-catenin, accumulates throughout GSK3beta inhibitor treated tissues. Finally, experiments revealed increased cell proliferation in fin regenerates following LSN 2105786 treatment. Together, these data indicate that bone growth in zebrafish fin regeneration is improved by activating Wnt signaling. Zebrafish Wnt signaling experiments provide a good model to study bone growth and bone repair mechanisms, and may provide an efficient drug discovery platform.
机译:由于疾病,例如骨质疏松症,可能会损害骨骼生长。目前,间歇性甲状旁腺激素(PTH)治疗是美国唯一批准的骨质疏松症患者合成代谢骨生长疗法。 PTH治疗的合成代谢作用至少部分归因于Wnt /β-catenin途径的调节。以前显示使用小分子GSK3beta抑制剂激活Wnt /β-catenin途径会增加体外骨形成的标志物。我们的研究利用斑马鱼模型系统来研究Wnt激活的鳍再生和骨骼生长。 Wnt信号传导是鳍鳍再生的第一个遗传鉴定步骤,而骨射线是斑马鱼鳍鳍的主要结构。因此,斑马鱼鳍再生可能是研究Wnt信号介导的骨生长的有用模型。使用不同浓度的GSK3beta抑制剂化合物LSN 2105786进行鳍片再生实验,以用于不同的治疗时间,并在截肢后4天和7天测量再生的生长。实验表明,连续低浓度(4-5 nM)处理最有效地提高了再生能力。较高的浓度可能通过过度刺激分化程序而抑制了鳍的生长。进行原位杂交实验以检查GSK3beta抑制剂对Wnt反应基因表达的影响。实验表明,GSK3beta抑制剂治疗后单个基因标记的时空变化。另外,共聚焦显微镜和免疫荧光标记数据表明,Wnt信号细胞内信号转导子,β-catenin,在整个GSK3beta抑制剂治疗的组织中积累。最后,实验揭示了LSN 2105786处理后鳍再生中细胞增殖的增加。总之,这些数据表明,通过激活Wnt信号传导,可改善斑马鱼鳍再生中的骨骼生长。斑马鱼Wnt信号实验提供了研究骨骼生长和骨骼修复机制的良好模型,并可能提供有效的药物发现平台。

著录项

  • 作者

    Curtis, Courtney L.;

  • 作者单位

    Purdue University.;

  • 授予单位 Purdue University.;
  • 学科 Biology General.;Biology Cell.
  • 学位 M.S.
  • 年度 2013
  • 页码 51 p.
  • 总页数 51
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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