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从鼠诱导多能干细胞体外生成血管壁驻留的间充质多能干细胞。

In Vitro Generation of Vascular Wall-Resident Multipotent Stem Cells of Mesenchymal Nature from Murine Induced Pluripotent Stem Cells.

机构信息

Institute of Cell Biology (Cancer Research), University Hospital Essen, Medical Faculty, University of Duisburg-Essen, 45122 Essen, Germany.

Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, 45122 Essen, Germany.

出版信息

Stem Cell Reports. 2017 Apr 11;8(4):919-932. doi: 10.1016/j.stemcr.2017.03.001. Epub 2017 Mar 30.

Abstract

The vascular wall (VW) serves as a niche for mesenchymal stem cells (MSCs). In general, tissue-specific stem cells differentiate mainly to the tissue type from which they derive, indicating that there is a certain code or priming within the cells as determined by the tissue of origin. Here we report the in vitro generation of VW-typical MSCs from induced pluripotent stem cells (iPSCs), based on a VW-MSC-specific gene code. Using a lentiviral vector expressing the so-called Yamanaka factors, we reprogrammed tail dermal fibroblasts from transgenic mice containing the GFP gene integrated into the Nestin-locus (NEST-iPSCs) to facilitate lineage tracing after subsequent MSC differentiation. A lentiviral vector expressing a small set of recently identified human VW-MSC-specific HOX genes then induced MSC differentiation. This direct programming approach successfully mediated the generation of VW-typical MSCs with classical MSC characteristics, both in vitro and in vivo.

摘要

血管壁(VW)是间充质干细胞(MSCs)的龛位。一般来说,组织特异性干细胞主要向其来源的组织类型分化,这表明细胞内存在一定的代码或启动子,由起源组织决定。在这里,我们报告了基于 VW-MSC 特异性基因代码,从诱导多能干细胞(iPSCs)体外生成 VW 典型 MSCs。我们使用表达所谓的山中因子的慢病毒载体,重编程来自含有 GFP 基因整合到 Nestin 基因座的转基因小鼠尾部真皮成纤维细胞(NEST-iPSCs),以促进随后 MSC 分化后的谱系追踪。然后,表达一小组最近鉴定的人类 VW-MSC 特异性 HOX 基因的慢病毒载体诱导 MSC 分化。这种直接编程方法成功地介导了 VW 典型 MSCs 的生成,具有经典 MSC 的特征,无论是在体外还是体内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad1e/5390238/8e5692bfe24e/gr1.jpg

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