首页> 美国卫生研究院文献>Stem Cells International >BMSCs Interactions with Adventitial Fibroblasts Display Smooth Muscle Cell Lineage Potential in Differentiation and Migration That Contributes to Neointimal Formation
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BMSCs Interactions with Adventitial Fibroblasts Display Smooth Muscle Cell Lineage Potential in Differentiation and Migration That Contributes to Neointimal Formation

机译:骨髓间充质干细胞与优势成纤维细胞的相互作用显示出平滑肌细胞谱系潜能的分化和迁移有助于新内膜形成。

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摘要

In this study a model of simulated vascular injury in vitro was used to study the characterization of bone-marrow-derived mesenchymal stem cells (BMSCs) morphology and to investigate the differentiation and migration of BMSCs in the presence of adventitial fibroblasts. BMSCs from rats were indirectly cocultured with adventitial fibroblasts in a transwell chamber apparatus for 7 days, and clonogenic assays demonstrated that BMSCs could be differentiated into smooth muscle-like cells with this process, including smooth muscle α-actin (α-SMA) expression by immunofluorescence staining. Cell morphology of BMSCs was assessed by inverted microscope, while cell proliferation was assessed by MTT assay. The expressions of TGF-β1, MMP-1, and NF-κB were detected by immunofluorescence staining and Smad3 mRNA was measured by reverse transcription PCR. Migration ability of BMSCs with DAPI-labeled nuclei was measured by laser confocal microscopy. Our results demonstrate that indirect interactions with adventitial fibroblasts can induce proliferation, differentiation, and migration of BMSCs that can actively participate in neointimal formation. Our results indicate that the pathogenesis of vascular remodeling might perform via TGF-β1/Smad3 signal transduction pathways.
机译:在这项研究中,在体外模拟血管损伤模型用于研究骨髓来源的间充质干细胞(BMSCs)形态的特征,并研究在外膜成纤维细胞存在下BMSCs的分化和迁移。将大鼠的BMSC与外膜成纤维细胞在Transwell腔室装置中间接共培养7天,克隆形成试验表明,通过该过程,BMSC可以分化为平滑肌样细胞,包括通过以下途径表达平滑肌α-肌动蛋白(α-SMA)。免疫荧光染色。倒置显微镜评估BMSCs的细胞形态,MTT法评估细胞增殖。免疫荧光染色检测TGF-β1,MMP-1和NF-κB的表达,逆转录PCR检测Smad3 mRNA的表达。通过激光共聚焦显微镜测量具有DAPI标记核的BMSC的迁移能力。我们的结果表明,与外膜成纤维细胞的间接相互作用可以诱导BMSC的增殖,分化和迁移,而BMSC可以积极参与新内膜的形成。我们的结果表明,血管重塑的发病机制可能是通过TGF-β1/ Smad3信号转导途径进行的。

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