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The PLLA nanofibres displayed a significantly better proliferation rate, and enabled endothelial cells to proliferate in the monolayer.
Figure 3 indicates that better proliferation has occurred for glass-containing scaffolds.
Results showed that the construct had better proliferation and ECM secretion with bFGF.
On the apatite-coated composite scaffolds cells presented better proliferation than on apatite-coated chitosan scaffolds.
The higher efficiency of SF-mediated transfection compared to L2K was also correlated with better proliferation of cells.
The cytocompatibility test revealed better proliferation of mesenchymal stem cells on the nanofibrous mats than on the sponges.
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The amounts of proliferations were found slightly better than proliferation on hydrophilic graphene oxide (GO) sheets, and significantly higher than non-uniform proliferations on hydrophobic reduced graphene oxide (rGO) sheets and polydimethylsiloxane substrate.
However, better cell proliferation and differentiation were observed on the hMSC-encapsulated scaffolds compared to the hMSC-seeded scaffolds.
iPSC-derived MSCs (iMSCs) are also rejuvenated during the reprogramming process with better survival, proliferation and differentiations capabilities (Liu et al. 2013).
Bone marrow mesenchymal stem cells (MSCs) exhibited better adherence, proliferation and osteogenic phenotypes on nHA/PHB scaffolds than on PHB scaffolds.
The results showed that BMSC expressing BMP7 preferred a pore size between 100 and 300 μm in silk fibroin protein fabricated scaffolds, with better cell proliferation and ECM production.
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