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首页> 外文期刊>Journal of vascular research >Vascular cell-like potential of undifferentiated ligament fibroblasts to construct vascular cell-specific marker-positive blood vessel structures in a PI3K activation-dependent manner.
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Vascular cell-like potential of undifferentiated ligament fibroblasts to construct vascular cell-specific marker-positive blood vessel structures in a PI3K activation-dependent manner.

机译:未分化的韧带成纤维细胞的血管细胞样潜力以依赖PI3K激活的方式构建血管细胞特异性标志物阳性血管结构。

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摘要

OBJECTIVE: To evaluate whether fibroblasts derived from periodontal ligament retain the ability to differentiate into putative vascular cells and construct vascular cell-specific marker-positive blood vessel structures. We also evaluated the morphological features of the structure and investigated the intracellular molecular mechanism underlying the angiogenic activity of these cells. METHODS: Single cell-derived cultures (SCDCs) were established from primary rat ligament fibroblast cultures, and their expression of ligament cell-, mesenchymal stem cell- and vascular cell-specific markers was evaluated by RT-PCR and immunocytochemistry. The ability of the cells to construct a blood vessel structure was evaluated in a three-dimensional type I collagen scaffold. The morphological and immunohistological characteristics of the structure were then evaluated. RESULTS: Each SCDC expressed endothelial cell (EC)-specific and smooth muscle cell-specific markers, in addition to mesenchymal stem cell- and ligament cell-specific markers. SCDC2 cells, which abundantly expressed the EC markers Flk-1 and Tie-2, vigorously constructed a blood vessel structure in a phosphoinositide 3-kinase activation-dependent manner. CONCLUSION: Periodontal ligament fibroblasts have the potential to construct an EC marker-positive blood vessel-like structure. Consequently, the fibroblastic lineage in ligament tissue could be a candidate precursor for construction of a vascular system around damaged ligament tissue to facilitate its regeneration.
机译:目的:评价源自牙周膜的成纤维细胞是否仍具有分化为假定的血管细胞和构建血管细胞特异性标志物阳性血管结构的能力。我们还评估了该结构的形态学特征,并研究了这些细胞的血管生成活性背后的细胞内分子机制。方法:从原代大鼠韧带成纤维细胞培养物中建立单细胞来源的培养物(SCDC),并通过RT-PCR和免疫细胞化学方法评估它们在韧带细胞,间充质干细胞和血管细胞中的表达。在三维I型胶原蛋白支架中评估了细胞构建血管结构的能力。然后评估该结构的形态学和免疫组织学特征。结果:除了间充质干细胞和韧带细胞特异性标记外,每个SCDC还表达了内皮细胞(EC)特异性和平滑肌细胞特异性标记。大量表达EC标记Flk-1和Tie-2的SCDC2细胞以磷酸肌醇3激酶激活依赖性方式强烈构建了血管结构。结论:牙周膜成纤维细胞具有构建EC标志物阳性血管样结构的潜力。因此,韧带组织中的成纤维细胞谱系可以是在受损的韧带组织周围构造血管系统以促进其再生的候选前体。

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