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微小RNA调控小鼠骨髓基质细胞的成骨和成软骨作用。

MicroRNAs regulate osteogenesis and chondrogenesis of mouse bone marrow stromal cells.

作者信息

Suomi Salla, Taipaleenmäki Hanna, Seppänen Anne, Ripatti Tommi, Väänänen Kalervo, Hentunen Teuvo, Säämänen Anna-Marja, Laitala-Leinonen Tiina

机构信息

Bone Biology Research Consortium, Department of Anatomy, Institute of Biomedicine, University of Turku, FI-20520, Finland.

出版信息

Gene Regul Syst Bio. 2008 Apr 22;2:177-91. doi: 10.4137/grsb.s662.

Abstract

MicroRNAs (miRNAs) are non-coding RNAs that bind to target mRNA leading to translational arrest or mRNA degradation. To study miRNA-mediated regulation of osteogenesis and chondrogenesis, we compared the expression of 35 miRNAs in osteoblasts and chondroblasts derived from mouse marrow stromal cells (MSCs). Differentiation of MSCs resulted in up- or downregulation of several miRNAs, with miR-199a expression being over 10-fold higher in chondroblasts than in undifferentiated MSCs. In addition, miR-124a was strongly upregulated during chondrogenesis while the expression of miR-96 was substantially suppressed. A systems biological analysis of the potential miRNA target genes and their interaction networks was combined with promoter analysis. These studies link the differentially expressed miRNAs to collagen synthesis and hypoxia, key pathways related to bone and cartilage physiology. The global regulatory networks described here suggest for the first time how miRNAs and transcription factors are capable of fine-tuning the osteogenic and chondrogenic differentiation of mouse MSCs.

摘要

微小RNA(miRNA)是一类非编码RNA,可与靶mRNA结合,导致翻译停滞或mRNA降解。为了研究miRNA介导的成骨和成软骨调节作用,我们比较了从小鼠骨髓基质细胞(MSC)衍生的成骨细胞和软骨细胞中35种miRNA的表达情况。MSC的分化导致几种miRNA的上调或下调,其中miR-199a在软骨细胞中的表达比未分化的MSC高10倍以上。此外,miR-124a在软骨形成过程中强烈上调,而miR-96的表达则被显著抑制。对潜在的miRNA靶基因及其相互作用网络进行了系统生物学分析,并结合了启动子分析。这些研究将差异表达的miRNA与胶原蛋白合成和缺氧联系起来,这是与骨骼和软骨生理相关的关键途径。这里描述的全局调控网络首次表明miRNA和转录因子如何能够微调小鼠MSC的成骨和成软骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52ed/2733092/1c5964dbfad0/grsb-2008-177f1.jpg

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