Combinations of growth factors for human mesenchymal stem cell proliferation and osteogenic differentiation

肝细胞生长因子 生长因子 间充质干细胞 细胞生长 细胞生物学 血管内皮生长因子 碱性成纤维细胞生长因子 碱性磷酸酶 细胞外基质 转化生长因子 生物 成纤维细胞生长因子 细胞分化 化学 受体 癌症研究 生物化学 血管内皮生长因子受体 基因
作者
Veronika Hefka Blahnová,Jana Daňková,Michala Rampichová,Eva Filová
出处
期刊:Bone and Joint Research [Journal of Bone and Joint Surgery]
卷期号:9 (7): 412-420 被引量:32
标识
DOI:10.1302/2046-3758.97.bjr-2019-0183.r2
摘要

Here we introduce a wide and complex study comparing effects of growth factors used alone and in combinations on human mesenchymal stem cell (hMSC) proliferation and osteogenic differentiation. Certain ways of cell behaviour can be triggered by specific peptides - growth factors, influencing cell fate through surface cellular receptors.In our study transforming growth factor β (TGF-β), basic fibroblast growth factor (bFGF), hepatocyte growth factor (HGF), insulin-like growth factor 1 (IGF-1), and vascular endothelial growth factor (VEGF) were used in order to induce osteogenesis and proliferation of hMSCs from bone marrow. These cells are naturally able to differentiate into various mesodermal cell lines. Effect of each factor itself is pretty well known. We designed experimental groups where two and more growth factors were combined. We supposed cumulative effect would appear when more growth factors with the same effect were combined. The cellular metabolism was evaluated using MTS assay and double-stranded DNA (dsDNA) amount using PicoGreen assay. Alkaline phosphatase (ALP) activity, as early osteogenesis marker, was observed. Phase contrast microscopy was used for cell morphology evaluation.TGF-β and bFGF were shown to significantly enhance cell proliferation. VEGF and IGF-1 supported ALP activity. Light microscopy showed initial extracellular matrix mineralization after VEGF/IGF-1 supply.A combination of more than two growth factors did not support the cellular metabolism level and ALP activity even though the growth factor itself had a positive effect. This is probably caused by interplay of various messengers shared by more growth factor signalling cascades.Cite this article: Bone Joint Res 2020;9(7):412-420.
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