4.6 Article

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

Journal

BONE & JOINT RESEARCH
Volume 9, Issue 7, Pages 412-420

Publisher

BRITISH EDITORIAL SOC BONE & JOINT SURGERY
DOI: 10.1302/2046-3758.97.BJR-2019-0183.R2

Keywords

Mesenchymal stem cell; Growth factor; Osteogenic differentiation; Regenerative medicine

Funding

  1. Grant Agency of Charles University [448218]
  2. Ministry of Education, Youth and Sports of the Czech Republic within National Sustainability Programme I [RP NPUI:LO1508, RP NPU-I:LO1309, CZ.2.16/3.1.00/24006]
  3. Czech Science Foundation [18 to 09306 S]
  4. Internal Grant Agency of the Ministry of Health of the Czech Republic [NV18-05-00379, 16-28637A, 17-32285A]

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Aims 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. Methods In our study transforming growth factor beta (TGF-beta), 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. Results TGF-beta 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. Conclusion 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.

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