Effect of donor variation on osteogenesis and vasculogenesis in hydrogel cocultures.
Iris PenningsLukas A van DijkJuliet van HuukslootJoost O FledderusKoen SchepersA Koen BraatEdward C HsiaoEmilie BarruetBlanca M MoralesMarianne Christina VerhaarAntoine J W P RosenbergDebby GawlittaPublished in: Journal of tissue engineering and regenerative medicine (2019)
To introduce a functional vascular network into tissue-engineered bone equivalents, human endothelial colony forming cells (ECFCs) and multipotent mesenchymal stromal cells (MSCs) can be cocultured. Here, we studied the impact of donor variation of human bone marrow-derived MSCs and cord blood-derived ECFCs on vasculogenesis and osteogenesis using a 3D in vitro coculture model. Further, to make the step towards cocultures consisting of cells derived from a single donor, we tested how induced pluripotent stem cell (iPSC)-derived human endothelial cells (iECs) performed in coculture models. Cocultures with varying combinations of human donors of MSCs, ECFCs, or iECs were prepared in Matrigel. The constructs were cultured in an osteogenic differentiation medium. Following a 10-day culture period, the length of the prevascular structures and osteogenic differentiation were evaluated for up to 21 days of culture. The particular combination of MSC and ECFC donors influenced the vasculogenic properties significantly and induced variation in osteogenic potential. In addition, the use of iECs in the cocultures resulted in prevascular structure formation in osteogenically differentiated constructs. Together, these results showed that close attention to the source of primary cells, such as ECFCs and MSCs, is critical to address variability in vasculogenic and osteogenic potential. The 3D coculture model appeared to successfully generate prevascularized constructs and were sufficient in exceeding the ~200 μm diffusion limit. In addition, iPSC-derived cell lineages may decrease variability by providing a larger and potentially more uniform source of cells for future preclinical and clinical applications.
Keyphrases
- endothelial cells
- mesenchymal stem cells
- high glucose
- induced apoptosis
- bone marrow
- induced pluripotent stem cells
- cell cycle arrest
- stem cells
- umbilical cord
- cord blood
- endoplasmic reticulum stress
- oxidative stress
- pluripotent stem cells
- signaling pathway
- vascular endothelial growth factor
- diabetic rats
- working memory
- single cell
- pi k akt
- postmenopausal women
- drug induced
- soft tissue
- mass spectrometry
- network analysis