首页> 美国卫生研究院文献>other >Fluorescent Activated Cell Sorting (FACS) Combined with Gene Expression Microarrays for Transcription Enrichment Profiling of Zebrafish Lateral Line Cells
【2h】

Fluorescent Activated Cell Sorting (FACS) Combined with Gene Expression Microarrays for Transcription Enrichment Profiling of Zebrafish Lateral Line Cells

机译:荧光激活细胞分选(FACS)结合基因表达微阵列的斑马鱼侧线细胞转录富集分析。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Transgenic lines carrying fluorescent reporter genes like GFP have been of great value in the elucidation of developmental features and physiological processes in various animal models, including zebrafish. The lateral line (LL), which is a fish specific superficial sensory organ, is an emerging organ model for studying complex cellular processes in the context of the whole living animal. Cell migration, mechanosensory cell development/differentiation and regeneration are some examples. This sensory system is made of superficial and sparse small sensory patches called neuromasts, with less than 50 cells in any given patch. The paucity of cells is a real problem in any effort to characterize those cells at the transcriptional level. We describe here a method which we applied to efficiently separate subpopulation of cells of the LL, using two distinct stable transgenic zebrafish lines, Tg(cldnb:gfp) and Tg(tnks1bp1:EGFP). In both cases, the GFP positive (GFP+) cells were separated from the remainder of the animal by using a Fluorescent Activated Cell Sorter (FACS). The transcripts of the GFP+ cells were subsequently analyzed on gene expression microarrays. The combination of FACS and microarrays is an efficient method to establish a transcriptional signature for discrete cell populations which would otherwise be masked in whole animal preparation.
机译:带有荧光报告基因如GFP的转基因品系在阐明包括斑马鱼在内的各种动物模型的发育特征和生理过程中具有重要价值。侧线(LL)是鱼类特有的表面感觉器官,是一种新兴的器官模型,用于研究整个活体动物中的复杂细胞过程。细胞迁移,机械感觉细胞发育/分化和再生是一些例子。这种感觉系统由称为神经质的浅表和稀疏的小感觉斑块组成,每个给定斑块中的细胞少于50个。在以转录水平表征这些细胞的任何努力中,细胞的缺乏都是一个真正的问题。我们在这里描述了一种方法,我们使用两个不同的稳定转基因斑马鱼品系Tg(cldnb:gfp)和Tg(tnks1bp1:EGFP)有效地分离了LL细胞的亚群。在这两种情况下,通过使用荧光激活细胞分选仪(FACS)将GFP阳性(GFP +)细胞与动物的其余部分分离。随后在基因表达微阵列上分析GFP +细胞的转录本。 FACS和微阵列的组合是一种为离散细胞群体建立转录特征的有效方法,否则该突变将在整个动物制备过程中被掩盖。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号