Reprogramming hMSCs morphology with silicon/porous silicon geometric micro-patterns

• Published in: Biomedical microdevices 2014-04, Vol.16 (2), p.229-236
• Main Authors: Ynsa, M. D., Dang, Z. Y., Manso-Silvan, M., Song, J., Azimi, S., Wu, J. F., Liang, H. D., Torres-Costa, V., Punzon-Quijorna, E., Breese, M. B. H., Garcia-Ruiz, J. P.
• Format: Article
• Language: English
• Subjects: Biological and Medical Physics; Biomedical engineering; Biomedical Engineering and Bioengineering; Biophysics; Bones; Cell Culture Techniques - instrumentation; Cell Culture Techniques - methods; Cells, Cultured; Cellular biology; Cellular Reprogramming; Core Binding Factor Alpha 1 Subunit - genetics; Core Binding Factor Alpha 1 Subunit - metabolism; Engineering; Engineering Fluid Dynamics; Hexagons; Human; Humans; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - metabolism; Morphology; Nanotechnology; Networks; Porosity; Porous silicon; Receptors, Calcitriol - genetics; Receptors, Calcitriol - metabolism; Silicon; Silicon - chemistry; Silicon substrates; Stem cells; Vitamins
• ISSN: 1387-2176; 1572-8781
• DOI: 10.1007/s10544-013-9826-0

Geometric micro-patterned surfaces of silicon combined with porous silicon (Si/PSi) have been manufactured to study the behaviour of human Mesenchymal Stem Cells (hMSCs). These micro-patterns consist of regular silicon hexagons surrounded by spaced columns of silicon equilateral triangles separated by PSi. The results show that, at an early culture stage, the hMSCs resemble quiescent cells on the central hexagons with centered nuclei and actin/β-catenin and a microtubules network denoting cell adhesion. After 2 days, hMSCs adapted their morphology and cytoskeleton proteins from cell-cell dominant interactions at the center of the hexagonal surface. This was followed by an intermediate zone with some external actin fibres/β-catenin interactions and an outer zone where the dominant interactions are cell-silicon. Cells move into silicon columns to divide, migrate and communicate. Furthermore, results show that Runx2 and vitamin D receptors, both specific transcription factors for skeleton-derived cells, are expressed in cells grown on micropatterned silicon under all observed circumstances. On the other hand, non-phenotypic alterations are under cell growth and migration on Si/PSi substrates. The former consideration strongly supports the use of micro-patterned silicon surfaces to address pending questions about the mechanisms of human bone biogenesis/pathogenesis and the study of bone scaffolds.