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脊索细胞在胚胎形成髓核过程中的全转录组分析。

Whole Transcriptome Analysis of Notochord-Derived Cells during Embryonic Formation of the Nucleus Pulposus.

机构信息

Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Sci Rep. 2017 Sep 5;7(1):10504. doi: 10.1038/s41598-017-10692-5.

Abstract

Recapitulation of developmental signals represents a promising strategy for treating intervertebral disc degeneration. During development, embryonic notochord-derived cells (NDCs) are the direct progenitors of cells that populate the adult nucleus pulposus (NP) and are an important source of secreted signaling molecules. The objective of this study was to define global gene expression profiles of NDCs at key stages of embryonic disc formation. NDCs were isolated from Shh-cre;ROSA:YFP mice at embryonic day 12.5 and postnatal day 0, representing opposite ends of the notochord to NP transformation. Differences in global mRNA abundance across this developmental window were established using RNA-Seq. Protein expression of selected molecules was confirmed using immunohistochemistry. Principal component analysis revealed clustering of gene expression at each developmental stage with more than 5000 genes significantly differentially expressed between E12.5 and P0. There was significantly lower mRNA abundance of sonic hedgehog pathway elements at P0 vs E12.5, while abundance of elements of the transforming growth factor-beta and insulin-like growth factors pathways, and extracellular matrix components including collagen 6 and aggrecan, were significantly higher at P0. This study represents the first transcriptome-wide analysis of embryonic NDCs. Results suggest signaling and biosynthesis of NDCs change dramatically as a function of developmental stage.

摘要

发育信号的重现将成为治疗椎间盘退变的有前途的策略。在发育过程中,胚胎脊索源性细胞(NDC)是成年核髓核(NP)细胞的直接前体细胞,是分泌信号分子的重要来源。本研究的目的是定义胚胎椎间盘形成关键阶段 NDC 的全基因表达谱。从 Shh-cre;ROSA:YFP 小鼠中分离出 E12.5 和 P0 天的 NDC,代表脊索到 NP 转化的相反端。使用 RNA-Seq 确定了整个发育窗口中全局 mRNA 丰度的差异。使用免疫组织化学法证实了选定分子的蛋白质表达。主成分分析显示在每个发育阶段的基因表达聚类,E12.5 和 P0 之间有超过 5000 个基因显著差异表达。与 E12.5 相比,P0 时 sonic hedgehog 通路元件的 mRNA 丰度显著降低,而转化生长因子-β和胰岛素样生长因子通路的元件以及细胞外基质成分(包括胶原 6 和聚集蛋白聚糖)的丰度在 P0 时显著增加。本研究代表了对胚胎 NDC 进行的全转录组分析。结果表明,NDC 的信号和生物合成随发育阶段的变化而显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db66/5585380/774d41015278/41598_2017_10692_Fig1_HTML.jpg

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