首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Angiogenic potential of human mesenchymal stromal cell and circulating mononuclear cell cocultures is reflected in the expression profiles of proangiogenic factors leading to endothelial cell and pericyte differentiation
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Angiogenic potential of human mesenchymal stromal cell and circulating mononuclear cell cocultures is reflected in the expression profiles of proangiogenic factors leading to endothelial cell and pericyte differentiation

机译:人间充质基质细胞和循环单核细胞共培养物的血管生成潜力反映在导致内皮细胞和细胞分化的常规因子的表达谱中

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Abstract Endothelial progenitors found among the peripheral blood (PB) mononuclear cells (MNCs) are interesting cells for their angiogenic properties. Mesenchymal stromal cells (MSCs) in turn can produce proangiogenic factors as well as differentiate into mural pericytes, making MSCs and MNCs an attractive coculture setup for regenerative medicine. In this study, human bone marrow‐derived MSCs and PB‐derived MNCs were cocultured in basal or osteoblastic medium without exogenously supplied growth factors to demonstrate endothelial cell, pericyte and osteoblastic differentiation. The expression levels of various proangiogenic factors, as well as endothelial cell, pericyte and osteoblast markers in cocultures were determined by quantitative polymerase chain reaction. Immunocytochemistry for vascular endothelial growth factor receptor‐1 and α‐smooth muscle actin as well as staining for alkaline phosphatase were performed after 10 and 14?days. Messenger ribonucleic acid expression of endothelial cell markers was highly upregulated in both basal and osteoblastic conditions after 5?days of coculture, indicating an endothelial cell differentiation, which was supported by immunocytochemistry for vascular endothelial growth factor receptor‐1. Stromal derived factor‐1 and vascular endothelial growth factor were highly expressed in MSC‐MNC coculture in basal medium but not in osteoblastic medium. On the contrary, the expression levels of bone morphogenetic protein‐2 and angiopoietin‐1 were significantly higher in osteoblastic medium. Pericyte markers were highly expressed in both cocultures after 5?days. In conclusion, it was demonstrated endothelial cell and pericyte differentiation in MSC‐MNC cocultures both in basal and osteoblastic medium indicating a potential for neovascularization for tissue engineering applications.
机译:摘要外周血(PB)单核细胞(MNC)中发现的内皮祖细胞是有趣的细胞,用于其血管生成特性。间充质基质细胞(MSCs)又可以产生常规因子,以及分化成壁质周细胞,使MSC和MNCS成为再生医学的吸引力的共培养设置。在该研究中,人骨髓衍生的MSCs和PB衍生的MNC在基础或骨细胞培养基中通过外源供应生长因子来培养,以证明内皮细胞,周刊和骨细胞分化。通过定量聚合酶链式反应测定各种常规因子的表达水平,以及共培养物中的内皮细胞,内皮细胞和成骨细胞标记物。血管内皮生长因子受体-1和α-平滑肌肌动蛋白的免疫细胞化学以及碱性磷酸酶染色后10-14天进行。在培养的5?天数之后的基础和骨细胞条件下,内皮细胞标记物的信使核糖核核酸表达高度上调,表明内皮细胞分化,其被用于血管内皮生长因子受体-1的免疫细胞化学支持。基质衍生因子-1和血管内皮生长因子在基础培养基中的MSC-MNC共培养物中高度表达,但不在骨细胞介质中。相反,骨髓细胞介质中骨形态发生蛋白-2和血管生成素-1的表达水平显着较高。在5?天后的共科卢比中,细胞标记物高度表达。总之,在基础和成骨细胞介质中,在MSC-MNC培养基中证明了内皮细胞和细胞分化,这表明用于组织工程应用的新血管形成的潜力。

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